-
1
-
-
72449131828
-
-
OMIM HD
-
OMIM 143 100: HUNTINGTON DISEASE; HD
-
Huntington Disease
, vol.143
, pp. 100
-
-
-
2
-
-
0023187041
-
Epidemiologic study of Huntington disease in the catchment area of the Wurzburg University Neurologic Clinic with special reference to the Lower Franconia district
-
Przuntek H, Steigerwald A. Epidemiologic study of Huntington disease in the catchment area of the Wurzburg University Neurologic Clinic with special reference to the Lower Franconia district. Nervenarzt 1987; 58: 424-427
-
(1987)
Nervenarzt
, vol.58
, pp. 424-427
-
-
Przuntek, H.1
Steigerwald, A.2
-
3
-
-
0017656989
-
Electron spin resonance study of membrane protein alterations in erythrocytes in Huntington's disease
-
Butterfield DA, Oeswein JQ, Markesbery WR. Electron spin resonance study of membrane protein alterations in erythrocytes in Huntington's disease. Nature 1977; 267: 453-455
-
(1977)
Nature
, vol.267
, pp. 453-455
-
-
Butterfield, D.A.1
Oeswein, J.Q.2
Markesbery, W.R.3
-
5
-
-
0022645873
-
Spin label study of red blood cell membranes in Huntington's disease
-
Kraus PH, Vigenschow H, Przuntek H. Spin label study of red blood cell membranes in Huntington's disease. Eur Neurol 1986; 25: 61-66 (Pubitemid 16208303)
-
(1986)
European Neurology
, vol.25
, Issue.1
, pp. 61-66
-
-
Kraus, P.H.1
Vigenschow, H.2
Przuntek, H.3
-
6
-
-
0021289459
-
2O molecules across membranes of erythrocyte ghosts from patients with Huntington's disease and from normal individuals
-
Vigenschow H, Przuntek H, Lawaczeck R. On the exchange of H20/ D20 molecules across membranes of erythrocyte ghosts from patients with Huntington's disease and from normal individuals. J Neurol 1984; 231: 54-55 (Pubitemid 14196249)
-
(1984)
Journal of Neurology
, vol.231
, Issue.1
, pp. 54-55
-
-
Vigenschow, H.1
Przuntek, H.2
Lawaczeck, R.3
-
8
-
-
0021349731
-
Huntington's disease: Biochemical prediction by determination of GABA synthesis of cultured fibroblasts
-
Gohlich G, Kuhn W, Hohn H et al. Huntington's disease: biochemical prediction by determination of GABA synthesis of cultured fibroblasts.J Neurol 1984; 231: 50-51
-
(1984)
J Neurol
, vol.231
, pp. 50-51
-
-
Gohlich, G.1
Kuhn, W.2
Hohn, H.3
-
9
-
-
0018580183
-
GABA synthesis by cultured fibroblasts obtained from persons with Huntington's disease
-
Gray PN, Dana SL GABA synthesis by cultured fibroblasts obtained from persons with Huntington's disease. J Neurochem 1979; 33: 985-992
-
(1979)
J Neurochem
, vol.33
, pp. 985-992
-
-
Gray, P.N.1
Dana, S.L.2
-
10
-
-
0019774040
-
3H]muscimol radioreceptor assay
-
Hamel E, Goetz IE, Roberts E. Glutamic acid decarboxylase and gamma-aminobutyric acid in Huntington's disease fibroblasts and other cultured cells, determined by a [3H]muscimol radioreceptor assay. J Neurochem 1981; 37: 1032-1038 (Pubitemid 12209343)
-
(1981)
Journal of Neurochemistry
, vol.37
, Issue.4
, pp. 1032-1038
-
-
Hamel, E.1
Goetz, I.E.2
Roberts, E.3
-
11
-
-
84959787530
-
Huntington's chorea
-
Post-mortem measurement of glutamic acid decarboxylase, choline acetyltransferase and dopamine in basal ganglia.
-
Bird ED, Iversen LL. Huntington's chorea. Post-mortem measurement of glutamic acid decarboxylase, choline acetyltransferase and dopamine in basal ganglia. Brain 1974; 97: 457-472
-
(1974)
Brain
, vol.97
, pp. 457-472
-
-
Bird, E.D.1
Iversen, L.L.2
-
12
-
-
0015790444
-
Deficiency of gamma-aminobutyricacid in brain
-
Huntington's chorea.
-
Perry TL, Hansen S, Kloster M. Huntington's chorea. Deficiency of gamma-aminobutyricacid in brain. N EnglJ Med 1973; 288: 337-342
-
(1973)
N Engl J Med
, vol.288
, pp. 337-342
-
-
Perry, T.L.1
Hansen, S.2
Kloster, M.3
-
13
-
-
0023258197
-
Decreased glutamic acid and increased 5-hydroxytryptamine in Huntington's disease brain
-
Reynolds GP, Pearson SJ. Decreased glutamic acid and increased 5-hydroxytryptamine in Huntington's disease brain. Neurosci Lett 1987; 78:233-238
-
(1987)
Neurosci Lett
, vol.78
, pp. 233-238
-
-
Reynolds, G.P.1
Pearson, S.J.2
-
14
-
-
0018973928
-
Neurochemical alterations in Huntington's chorea. A study of post mortem brain tissue
-
Spokes EG. Neurochemical alterations in Huntington's chorea: a study of post-mortem brain tissue. Brain 1980; 103: 179-210 (Pubitemid 10009481)
-
(1980)
Brain
, vol.103
, Issue.1
, pp. 179-210
-
-
Spokes, E.G.S.1
-
15
-
-
0023269358
-
Elevated serotonin and reduced dopamine in subregionally divided Huntington's disease striatum
-
Kish SJ, Shannak K, Hornykiewicz O. Elevated serotonin and reduced dopamine in subregionally divided Huntington's disease striatum. Ann Neurol 1987; 22: 386-389 (Pubitemid 17137904)
-
(1987)
Annals of Neurology
, vol.22
, Issue.3
, pp. 386-389
-
-
Kish, S.J.1
Shannak, K.2
Hornykiewicz, O.3
-
16
-
-
0017183963
-
Morphometric studies of the neuropathological changes in choreatic diseases
-
Lange H, Thorner G, Hopf A et al. Morphometric studies of the neuropathological changes in choreatic diseases. J Neurol Sei 1976; 28: 401-425
-
(1976)
J Neurol Sei
, vol.28
, pp. 401-425
-
-
Lange, H.1
Thorner, G.2
Hopf, A.3
-
17
-
-
0021982117
-
Evidence for degenerative and regenerative changes in neostriatal spiny neurons in Huntington's disease
-
Graveland GA, Williams RS, DiFiglia M. Evidence for degenerative and regenerative changes in neostriatal spiny neurons in Huntington's disease. Science 1985; 227: 770-773 (Pubitemid 15168268)
-
(1985)
Science
, vol.227
, Issue.4688
, pp. 770-773
-
-
Graveland, G.A.1
Williams, R.S.2
Difiglia, M.3
-
18
-
-
0022876328
-
Huntington's disease. Pathogenesis and management
-
Martin JB, Gusella JF. Huntington's disease. Pathogenesis and management. N Engl J Med 1986; 315: 1267-1276
-
(1986)
N Engl J Med
, vol.315
, pp. 1267-1276
-
-
Martin, J.B.1
Gusella, J.F.2
-
19
-
-
0022527062
-
Opioid peptides in Huntington's disease: Alterations in prodynorphin and proenkephalin system
-
DOI 10.1016/0006-8993(86)90946-7
-
Seizinger BR, Liebisch DC, Kish SJ et al. Opioid peptides in Huntington's disease: alterations in prodynorphin and proenkephalin system. Brain Res 1986; 378: 405-408 (Pubitemid 16055581)
-
(1986)
Brain Research
, vol.378
, Issue.2
, pp. 405-408
-
-
Seizinger, B.R.1
Liebisch, D.C.2
Kish, S.J.3
-
20
-
-
0001891547
-
The neurobiology of Huntington's disease
-
Harper PS. Second Edition. London: WP Saunders
-
MacMillan JC, Quarrell OWJ. The neurobiology of Huntington's disease. In: Harper PS. Huntington's disease. Second Edition. London: WP Saunders, 1996:317-357
-
(1996)
Huntington's Disease.
, pp. 317-357
-
-
MacMillan, J.C.1
Quarrell, O.W.J.2
-
21
-
-
0028978124
-
Striatal D1 and D2 receptor binding in patients with Huntington's disease and other choreas
-
Turjanski N, Weeks R, Dolan R et al. Striatal D1 and D2 receptor binding in patients with Huntington's disease and other choreas. A PET study. Brain 1995; 118: 689-696
-
(1995)
A PET Study. Brain
, vol.118
, pp. 689-696
-
-
Turjanski, N.1
Weeks, R.2
Dolan, R.3
-
22
-
-
0029895292
-
Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease
-
Weeks RA, Piccini P, Harding AE et al. Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease. Ann Neurol 1996; 40: 49-54
-
(1996)
Ann Neurol
, vol.40
, pp. 49-54
-
-
Weeks, R.A.1
Piccini, P.2
Harding, A.E.3
-
23
-
-
0023690166
-
NMDA receptor losses in putamen from patients with Huntington's disease
-
Young AB, Greenamyre JT, Hollingsworth Z et al. NMDA receptor losses in putamen from patients with Huntington's disease. Science 1988; 241:981-983
-
(1988)
Science
, vol.241
, pp. 981-983
-
-
Young, A.B.1
Greenamyre, J.T.2
Hollingsworth, Z.3
-
24
-
-
0025322132
-
Abnormalities of striatal projection neurons and N-methyl-D-aspartate receptors in presymptomatic Huntington's disease
-
Albin RL Young AB, Penney JB et al. Abnormalities of striatal projection neurons and N-methyl-D-aspartate receptors in presymptomatic Huntington's disease. N engl J Med 1990; 322: 1293-1298
-
(1990)
N Engl J Med
, vol.322
, pp. 1293-1298
-
-
Albin, R.L.1
Young, A.B.2
Penney, J.B.3
-
25
-
-
0032568517
-
Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human huntington disease gene
-
Cha JH, Kosinski CM, Kerner JA et al. Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human huntington disease gene. PNAS (USA) 1998; 95: 6480-6485
-
(1998)
PNAS (USA)
, vol.95
, pp. 6480-6485
-
-
Cha, J.H.1
Kosinski, C.M.2
Kerner, J.A.3
-
26
-
-
0033210254
-
Huntington chorea
-
Animal models reveal new hypotheses for pathophysiology and therapy
-
Kosinski CM, Cha JH, Young AB et al. Huntington chorea. Animal models reveal new hypotheses for pathophysiology and therapy. Nervenarzt 1999; 70: 878-888
-
(1999)
Nervenarzt
, vol.70
, pp. 878-888
-
-
Kosinski, C.M.1
Cha, J.H.2
Young, A.B.3
-
27
-
-
0021028244
-
A polymorphic DNA marker genetically linked to Huntington's disease
-
Gusella JF, Wexler NS, Conneally PM et al. A polymorphic DNA marker genetically linked to Huntington's disease. Nature 1983; 306: 234-238
-
(1983)
Nature
, vol.306
, pp. 234-238
-
-
Gusella, J.F.1
Wexler, N.S.2
Conneally, P.M.3
-
28
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
The Huntington's Disease Collaborative Research Group
-
The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 1993; 72: 971-983
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
30
-
-
33748321965
-
Predictive testing for Huntington disease: Interpretation and significance of intermediate alleles
-
DOI 10.1111/j.1399-0004.2006.00668.x
-
Semaka A, Creighton S, Warby S et al. Predictive testing for Huntington disease: interpretation and significance of intermediate alleles. Clin Genet 2006; 70: 283-294 (Pubitemid 44323391)
-
(2006)
Clinical Genetics
, vol.70
, Issue.4
, pp. 283-294
-
-
Semaka, A.1
Creighton, S.2
Warby, S.3
Hayden, M.A.4
-
32
-
-
0032897901
-
Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism
-
DOI 10.1093/hmg/8.2.173
-
Leeflang EP, Tavare S, Marjoram P et al. Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism. Hum Mol Gen 1999; 8: 173-183 (Pubitemid 29054259)
-
(1999)
Human Molecular Genetics
, vol.8
, Issue.2
, pp. 173-183
-
-
Leeflang, E.P.1
Tavare, S.2
Marjoram, P.3
Neal, C.O.S.4
Srinidhi, J.5
MacDonald, M.E.6
Wexler, N.S.7
Gusella, J.F.8
Arnheim, N.9
-
33
-
-
0042307369
-
Huntington disease expansion mutations in humans can occur before meiosis is completed
-
Yoon SR, Dubeau L, deYoung M et al. Huntington disease expansion mutations in humans can occur before meiosis is completed. PNAS (USA) 2003; 100:8834-8838
-
(2003)
PNAS (USA)
, vol.100
, pp. 8834-8838
-
-
Yoon, S.R.1
Dubeau, L.2
Deyoung, M.3
-
35
-
-
33947729229
-
Biomarkers of neurodegeneration for diagnosis and monitoring therapeutics
-
DOI 10.1038/nrd2176, PII NRD2176
-
Shaw LM, Korecka M, Clark CM et al. Biomarkers of neurodegeneration for diagnosis and monitoring therapeutics. Nat Rev Drug Discov 2007; 6: 295-303 (Pubitemid 46505880)
-
(2007)
Nature Reviews Drug Discovery
, vol.6
, Issue.4
, pp. 295-303
-
-
Shaw, L.M.1
Korecka, M.2
Clark, C.M.3
Lee, V.M.-Y.4
Trojanowski, J.Q.5
-
36
-
-
85009332113
-
Unified Huntington's disease rating scale: Reliability and consistency
-
DOI 10.1002/mds.870110204
-
Huntington Study Group. Unified Huntington's Disease Rating Scale: reliability and consistency. Mov Disord 1996; 11:136-142 (Pubitemid 26082779)
-
(1996)
Movement Disorders
, vol.11
, Issue.2
, pp. 136-142
-
-
Kieburtz, K.1
-
37
-
-
0031740575
-
Unified Huntington's disease rating scale: A follow up
-
Siesling S, van Vugt JP, Zwlnderman KA et al. Unified Huntington's disease rating scale: a follow up. Mov Disord 1998; 13: 915-919 (Pubitemid 28517668)
-
(1998)
Movement Disorders
, vol.13
, Issue.6
, pp. 915-919
-
-
Siesling, S.1
Van Vugt, J.P.2
Zwinderman, K.A.H.3
Kieburtz, K.4
Roos, R.A.C.5
-
39
-
-
34248560852
-
Patients with Huntington's disease have impaired awareness of cognitive, emotional, and functional abilities
-
Hoth KF, Paulsen JS, Moser DJ et al. Patients with Huntington's disease have impaired awareness of cognitive, emotional, and functional abilities. J Clin Exp Neuropsychol 2007; 29: 365-376
-
(2007)
J Clin Exp Neuropsychol
, vol.29
, pp. 365-376
-
-
Hoth, K.F.1
Paulsen, J.S.2
Moser, D.J.3
-
40
-
-
0033650898
-
Subtle changes among presymptomatic carriers of the Huntington's disease gene
-
Kirkwood SC, Siemers E, Hodes ME et al. Subtle changes among presymptomatic carriers of the Huntington's disease gene. J Neurol Neurosurg Psychiatry 2000; 69: 773-779
-
(2000)
J Neurol Neurosurg Psychiatry
, vol.69
, pp. 773-779
-
-
Kirkwood, S.C.1
Siemers, E.2
Hodes, M.E.3
-
41
-
-
0031975912
-
Subtle involuntary movements are not reliable indicators of incipient Huntington's disease
-
DOI 10.1002/mds.870130120
-
De Boo G, Tibben A, Hermans J et al. Subtle involuntary movements are not reliable indicators of incipient Huntington's disease. Mov Disord 1998; 13: 96-99 (Pubitemid 28029859)
-
(1998)
Movement Disorders
, vol.13
, Issue.1
, pp. 96-99
-
-
De, B.1
Tibben, A.2
Hermans, J.3
Maat, A.4
Roos, R.A.C.5
-
43
-
-
20944438389
-
Interrater agreement in the assessment of motor manifestations of Huntington's disease
-
DOI 10.1002/mds.20332
-
Hogarth P, Kayson E, Kieburtz K et al. Interrater agreement in the assessment of motor manifestations of Huntington's disease. Mov Disord 2005; 20: 293-297 (Pubitemid 40613289)
-
(2005)
Movement Disorders
, vol.20
, Issue.3
, pp. 293-297
-
-
Hogarth, P.1
Kayson, E.2
Kieburtz, K.3
Marder, K.4
Oakes, D.5
Rosas, D.6
Shoulson, I.7
Wexler, N.S.8
Young, A.B.9
Zhao, H.10
Adler, C.11
Albin, R.12
Ashizawa, T.13
Bird, T.14
Blindauer, K.15
Bundlie, S.16
Caress, J.17
Caviness, J.18
Chouinard, S.19
Comella, C.20
Como, P.21
Corey-Bloom, J.22
Counihan, T.23
Deckel, W.24
Dubinsky, R.25
Duffy, J.26
Dure, L.27
Factor, S.28
Feigin, A.29
Fernandez, H.30
Friedman, J.31
Greenamyre, T.32
Guttman, M.33
Hauser, R.34
Hersch, S.35
Hersh, B.36
Hickenbottom, S.37
Higgins, D.38
Hobson, D.39
Jackson, G.40
Jankovic, J.41
Jennings, D.42
Johnson, W.43
Koller, W.44
Louis, E.45
Lafontaine, A.L.46
Leventhal, C.47
Mallonee, W.48
Marder, K.49
Marek, K.50
Martin, W.51
Mentis, M.52
Molho, E.53
Nance, M.54
O'Brien, C.55
Orme, C.56
Palmer, D.57
Paulsen, J.58
Paulson, G.59
Percy, A.60
Perlman, S.61
Perlmutter, J.62
Podskalny, G.63
Quiad, K.64
Racette, B.65
Rachez-Ramos, J.66
Raymond, L.67
Richman, D.68
Roberts, T.69
Rodnitzky, R.70
Ross, C.71
Rouleau, G.72
Rubin, A.73
Sax, D.74
Schimke, N.75
Shannon, K.76
Shelton, P.77
Shinaman, A.78
Shinobu, L.79
Shults, C.80
Siemers, E.81
Suchowersky, O.82
Walker, F.83
Weiner, W.84
Wheelock, V.85
Wojcieszek, J.86
Wooten, F.87
Bonilla, E.88
Cha, J.-H.89
Fischbeck, K.90
Negrette, A.91
Penney, J.B.92
Ramos, M.93
Snodgrass, R.94
Thompson, L.95
more..
-
44
-
-
33847607138
-
Change in MRI striatal volumes as a biomarker in preclinical Huntington's disease
-
Aylward EH. Change in MRI striatal volumes as a biomarker in preclinical Huntington's disease. Brain Res bull 2007; 72: 152-158
-
(2007)
Brain Res Bull
, vol.72
, pp. 152-158
-
-
Aylward, E.H.1
-
45
-
-
23844514798
-
Using advances in neuroimaging to detect, understand, and monitor disease progression in Huntington's disease
-
Rosas HD, Feigin AS, Hersch SM. Using advances in neuroimaging to detect, understand, and monitor disease progression in Huntington's disease. NeuroRx 2004; 1: 263-272
-
(2004)
NeuroRx
, vol.1
, pp. 263-272
-
-
Rosas, H.D.1
Feigin, A.S.2
Hersch, S.M.3
-
46
-
-
33645216173
-
Dose-dependent improvement of myoclonic hyperkinesia due to valproic acid in eight Huntington's disease patients: A case series
-
Saft C, Lauter T, Kraus PH et al. Dose-dependent improvement of myoclonic hyperkinesia due to valproic acid in eight Huntington's disease patients: a case series. BMC Neurology 2006; 6:11
-
(2006)
BMC Neurology
, vol.6
, pp. 11
-
-
Saft, C.1
Lauter, T.2
Kraus, P.H.3
-
47
-
-
0034711708
-
Rate of functional decline in Huntington's disease
-
Marder K, Zhao H, Myers RH et al. Rate of functional decline in Huntington's disease. Huntington Study Group. Neurology 2000; 54: 452-458 (Pubitemid 30078083)
-
(2000)
Neurology
, vol.54
, Issue.2
, pp. 452-458
-
-
Marder, K.1
Zhao, H.2
Myers, R.H.3
Cudkowicz, M.4
Kayson, E.5
Kieburtz, K.6
Orme, C.7
Paulsen, J.8
Penney Jr., J.B.9
Siemers, E.10
Shoulson, I.11
-
48
-
-
0032419075
-
Treatment of the psychiatric manifestations of Huntington's disease: A review of the literature
-
Leroi I, Michalon M. Treatment of the psychiatric manifestations of Huntington's disease: a review of the literature. Can J Psychiatry 1998; 43: 933-940 (Pubitemid 29173303)
-
(1998)
Canadian Journal of Psychiatry
, vol.43
, Issue.9
, pp. 933-940
-
-
Leroi, I.1
Michalon, M.2
-
49
-
-
0020954957
-
The association of affective disorder with Huntington's disease in a case series and in families
-
Folstein S, Abbott MH, Chase GA et al. The association of affective disorder with Huntington's disease in a case series and in families. Psychol Med 1983; 13: 537-542
-
(1983)
Psychol Med
, vol.13
, pp. 537-542
-
-
Folstein, S.1
Abbott, M.H.2
Chase, G.A.3
-
50
-
-
0036714830
-
Longitudinal personality changes among presymptomatic Huntington disease gene carriers
-
Kirkwood SC, Siemers E, Viken R et al. Longitudinal personality changes among presymptomatic Huntington disease gene carriers. Neuropsychiatry Neuropsychol Behav Neurol 2002; 15: 192-197 (Pubitemid 35006774)
-
(2002)
Neuropsychiatry, Neuropsychology and Behavioral Neurology
, vol.15
, Issue.3
, pp. 192-197
-
-
Kirkwood, S.C.1
Siemers, E.2
Viken, R.3
Hodes, M.E.4
Conneally, P.M.5
Christian, J.C.6
Foroud, T.7
-
52
-
-
0027934078
-
A controlled psychiatric study of individuals at risk for Huntington's disease
-
Shiwach RS, Norbury CG. A controlled psychiatric study of individuals at risk for Huntington's disease. Br J Psychiatry 1994; 165: 500-505 (Pubitemid 24305959)
-
(1994)
British Journal of Psychiatry
, vol.165
, Issue.OCT
, pp. 500-505
-
-
Shiwach, R.S.1
Norbury, C.G.2
-
53
-
-
33745110056
-
Preparing for preventive clinical trials: The predict-HD study
-
DOI 10.1001/archneur.63.6.883
-
Paulsen JS, Hayden M, Stout JC et al. Preparing for preventive clinical trials: the Predict-HD study. Arch Neurol 2006; 63: 883-890 (Pubitemid 43882298)
-
(2006)
Archives of Neurology
, vol.63
, Issue.6
, pp. 883-890
-
-
Paulsen, J.S.1
Hayden, M.2
Stout, J.C.3
Langbehn, D.R.4
Aylward, E.5
Ross, C.A.6
Guttman, M.7
Nance, M.8
Kieburtz, K.9
Oakes, D.10
Shoulson, I.11
Kayson, E.12
Johnson, S.13
Penziner, E.14
-
54
-
-
36549036813
-
Psychiatric Symptoms in Huntington's Disease before Diagnosis: The Predict-HD Study
-
DOI 10.1016/j.biopsych.2006.11.034, PII S0006322306015617
-
Duff K, PaulsenJS, Begllnger LJ et al. Psychiatric symptoms in Huntington's disease before diagnosis: the predict-HD study. Biol Psychiatry 2007; 62: 1341-1346 (Pubitemid 350180721)
-
(2007)
Biological Psychiatry
, vol.62
, Issue.12
, pp. 1341-1346
-
-
Duff, K.1
Paulsen, J.S.2
Beglinger, L.J.3
Langbehn, D.R.4
Stout, J.C.5
-
55
-
-
0035964234
-
Clinical markers of early disease in persons near onset of Huntington's disease
-
Paulsen JS, Zhao H, Stout JC et al. Clinical markers of early disease in persons near onset of Huntington's disease. Neurology 2001; 57: 658-662 (Pubitemid 32782994)
-
(2001)
Neurology
, vol.57
, Issue.4
, pp. 658-662
-
-
Paulsen, J.S.1
Zhao, H.2
Stout, J.C.3
Brinkman, R.R.4
Guttman, M.5
Ross, C.A.6
Como, P.7
Manning, C.8
Hayden, M.R.9
Shoulson, I.10
-
56
-
-
0031945107
-
Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriers
-
Hahn-Barma V, Deweer B, Durr A et al. Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriers. J Neurol Neurosurg Psychiatry 1998; 64: 172-177 (Pubitemid 28159797)
-
(1998)
Journal of Neurology Neurosurgery and Psychiatry
, vol.64
, Issue.2
, pp. 172-177
-
-
Hahn-Barma, V.1
Deweer, B.2
Durr, A.3
Dode, C.4
Feingold, J.5
Pillon, B.6
Agid, Y.7
Brice, A.8
Dubois, B.9
-
57
-
-
0017753313
-
Premorbid psychometric indicators of the gene for Huntington's disease
-
Lyle OE, Gottesman I.I.. Premorbid psychometric indicators of the gene for Huntington's disease. J Consult Clin Psychol 1977; 45: 1011-1022
-
(1977)
J Consult Clin Psychol
, vol.45
, pp. 1011-1022
-
-
Lyle, O.E.1
Gottesman, I.I.2
-
59
-
-
33847715903
-
Verbal episodic memory declines prior to diagnosis in Huntington's disease
-
Solomon AC, Stout JC, Johnson SA et al. Verbal episodic memory declines prior to diagnosis in Huntington's disease. Neuropsychologia 2007; 45: 1767-1776
-
(2007)
Neuropsychologia
, vol.45
, pp. 1767-1776
-
-
Solomon, A.C.1
Stout, J.C.2
Johnson, S.A.3
-
60
-
-
4344669917
-
Cognitive changes in patients with Huntington's disease (HD) and asymptomatic carriers of the HD mutation: A longitudinal follow-up study
-
Lemiere J, Decruyenaere M, Evers-Kiebooms G et al. Cognitive changes in patients with Huntington's disease (HD) and asymptomatic carriers of the HD mutation - a longitudinal follow-up study. J Neurol 2004; 251: 935-942 (Pubitemid 39119311)
-
(2004)
Journal of Neurology
, vol.251
, Issue.8
, pp. 935-942
-
-
Lemiere, J.1
Decruyenaere, M.2
Evers-Kiebooms, G.3
Vandenbussche, E.4
Dom, R.5
-
61
-
-
9144259577
-
Profile of cognitive progression in early Huntington's disease
-
Ho AK, Sahakian BJ, Brown RG et al. Profile of cognitive progression in early Huntington's disease. Neurology 2003; 61:1702-1706 (Pubitemid 38020815)
-
(2003)
Neurology
, vol.61
, Issue.12
, pp. 1702-1706
-
-
Ho, A.K.1
Sahakian, B.J.2
Brown, R.G.3
Barker, R.A.4
Hodges, J.R.5
Ane, M.-N.6
Snowden, J.7
Thompson, J.8
Esmonde, T.9
Gentry, R.10
Moore, J.W.11
Bodner, T.12
-
62
-
-
27744438097
-
Executive dysfunction in early stages of Huntington's disease is associated with striatal and insular atrophy: A neuropsychological and voxel-based morphometric study
-
DOI 10.1016/j.jns.2005.07.007, PII S0022510X05002650
-
Pelnemann A, Schuller S, Pohl C et al. Executive dysfunction in early stages of Huntington's disease is associated with striatal and insular atrophy: a neuropsychological and voxel-based morphometric study. J Neurol Sci 2005; 239: 11-19 (Pubitemid 41617410)
-
(2005)
Journal of the Neurological Sciences
, vol.239
, Issue.1
, pp. 11-19
-
-
Peinemann, A.1
Schuller, S.2
Pohl, C.3
Jahn, T.4
Weindl, A.5
Kassubek, J.6
-
63
-
-
18844422479
-
Disease co-varies with cognitive performance: A morphometric MRI analysis
-
Kassubek J, Juengllng FD, Ecker D et al. Thalamic atrophy in Huntington's disease co-varies with cognitive performance: a morphometric MRI analysis. Cereb Cortex 2005; 15: 846-853
-
(2005)
Cereb Cortex
, vol.15
, pp. 846-853
-
-
Kassubek, J.1
Juengllng, F.D.2
Ecker, D.3
-
64
-
-
0029431681
-
A prospective evaluation of cognitive decline in early Huntington's disease: Functional and radiographic correlates
-
Bamford KA, Calne ED, Kido DK et al. A prospective evaluation of cognitive decline in early Huntington's disease: functional and radiographic correlates. Neurology 1995; 45: 1867-1873
-
(1995)
Neurology
, vol.45
, pp. 1867-1873
-
-
Bamford, K.A.1
Calne, E.D.2
Kido, D.K.3
-
65
-
-
0024411737
-
Clinical-pathologic correlation in Huntington's disease: A neuropsychological and computed tomography study
-
Bamford KA, Caine ED, Kido DK et al. Clinical-pathologic correlation in Huntington's disease: a neuropsychological and computed tomography study. Neurology 1989; 39: 796-801 (Pubitemid 19150154)
-
(1989)
Neurology
, vol.39
, Issue.6
, pp. 796-801
-
-
Bamford, K.A.1
Caine, E.D.2
Kido, D.K.3
Plassche, W.M.4
Shoulson, I.5
-
66
-
-
0029987151
-
Single photon emission computed tomographic blood flow and magnetic resonance volume imaging of basal ganglia in Huntington's disease
-
Harris GJ, Aylward EH, Peyser CE et al. Single photon emission computed tomographic blood flow and magnetic resonance volume imaging of basal ganglia in Huntington's disease. Arch Neurol 1996; 53:316-324
-
(1996)
Arch Neurol
, vol.53
, pp. 316-324
-
-
Harris, G.J.1
Aylward, E.H.2
Peyser, C.E.3
-
68
-
-
0025971903
-
Cerebral structure on MRI, Part II: Specific changes in Alzheimer's and Huntington's diseases
-
Jernigan TL Salmon DP, Butters N et al. Cerebral structure on MRI, Part II: Specific changes in Alzheimer's and Huntington's diseases. Biol Psychiatry 1991; 29: 68-81
-
(1991)
Biol Psychiatry
, vol.29
, pp. 68-81
-
-
Jernigan, T.L.1
Salmon, D.P.2
Butters, N.3
-
69
-
-
0035118624
-
Longitudinal evaluation of cognitive disorder in Huntington's disease
-
DOI 10.1017/S1355617701711046
-
Snowden J, Craufurd D, Griffiths H et al. Longitudinal evaluation of cognitive disorder in Huntington's disease. J Int Neuropsychol Soc 2001; 7: 33-44 (Pubitemid 32177855)
-
(2001)
Journal of the International Neuropsychological Society
, vol.7
, Issue.1
, pp. 33-44
-
-
Snowden, J.1
Craufurd, D.2
Griffiths, H.3
Thompson, J.4
Neary, D.5
-
70
-
-
21744449768
-
White matter volume and cognitive dysfunction in early Huntington's disease
-
Beglinger LJ, Nopoulos PC, Jorge RE et al. White matter volume and cognitive dysfunction in early Huntington's disease. Cogn Behav Neurol 2005; 18: 102-107
-
(2005)
Cogn Behav Neurol
, vol.18
, pp. 102-107
-
-
Beglinger, L.J.1
Nopoulos, P.C.2
Jorge, R.E.3
-
71
-
-
0031950826
-
Frontal lobe volume in patients with Huntington's disease
-
Aylward EH, Anderson NB, Bylsma FWet al. Frontal lobe volume in patients with Huntington's disease. Neurology 1998; 50: 252-258 (Pubitemid 28106050)
-
(1998)
Neurology
, vol.50
, Issue.1
, pp. 252-258
-
-
Aylward, E.H.1
Anderson, N.B.2
Bylsma, F.W.3
Wagster, M.V.4
Barta, P.E.5
Sherr, M.6
Feeney, J.7
Davis, A.8
Rosenblatt, A.9
Pearlson, G.D.10
Ross, C.A.11
-
73
-
-
29944436350
-
Preclinical Huntington's disease: Compensatory brain responses during learning
-
DOI 10.1002/ana.20684
-
Feigin A, Ghilardi MF, Huang C et al. Preclinical Huntington's disease: compensatory brain responses during learning. Ann Neurol 2006; 59: 53-59 (Pubitemid 43042871)
-
(2006)
Annals of Neurology
, vol.59
, Issue.1
, pp. 53-59
-
-
Feigin, A.1
Ghilardi, M.-F.2
Huang, C.3
Ma, Y.4
Carbon, M.5
Guttman, M.6
Paulsen, J.S.7
Ghez, C.P.8
Eidelberg, D.9
-
74
-
-
0026465324
-
Reduced regional cerebral blood flow in Huntington's disease studied by SPECT
-
Hasselbalch SG, Oberg G, Sorensen SA et al. Reduced regional cerebral blood flow in Huntington's disease studied by SPECT. J Neurol Neurosurg Psychiatry 1992; 55: 1018-1023
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 1018-1023
-
-
Hasselbalch, S.G.1
Oberg, G.2
Sorensen, S.A.3
-
75
-
-
0022409202
-
Cerebral blood flow and cognitive testing correlate in Huntington's disease
-
Tanahashi N, Meyer JS, Ishikawa Yet al. Cerebral blood flow and cognitive testing correlate in Huntington's disease. Arch Neurol 1985; 42: 1169-1175
-
(1985)
Arch Neurol
, vol.42
, pp. 1169-1175
-
-
Tanahashi, N.1
Meyer, J.S.2
Ishikawa, Y.3
-
76
-
-
0023884580
-
Positron emission tomographic scan investigations of Huntington's disease: Cerebral metabolic correlates of cognitive function
-
Berent S, Giordani B, Lehtinen S et al. Positron emission tomographic scan investigations of Huntington's disease: cerebral metabolic correlates of cognitive function. Ann Neurol 1988; 23: 541-546
-
(1988)
Ann Neurol
, vol.23
, pp. 541-546
-
-
Berent, S.1
Giordani, B.2
Lehtinen, S.3
-
77
-
-
0025153344
-
Cortical and subcortical glucose consumption measured by PET in patients with Huntington's disease
-
Kuwert T, Lange HW, Langen KJ et al. Cortical and subcortical glucose consumption measured by PET in patients with Huntington's disease. Brain 1990; 113: 1405-1423 (Pubitemid 20385921)
-
(1990)
Brain
, vol.113
, Issue.5
, pp. 1405-1423
-
-
Kuwert, T.1
Lange, H.W.2
Langen, K.-J.3
Herzog, H.4
Aulich, A.5
Feinendegen, L.E.6
-
78
-
-
0025191509
-
2 receptors in Huntington's disease: Positron emission tomography findings and clinical correlates
-
Brandt J, Folstein SE, Wong DF et al. D2 receptors in Huntington's disease: positron emission tomography findings and clinical correlates. J Neurol Neurosurg Psychiatry 1990; 2: 20-27 (Pubitemid 20125840)
-
(1990)
Journal of Neuropsychiatry and Clinical Neurosciences
, vol.2
, Issue.1
, pp. 20-27
-
-
Brandt, J.1
Folstein, S.E.2
Wong, D.F.3
Links, J.4
Dannals, R.F.5
Starkstein, S.6
Anders, P.7
Strauss, M.E.8
Tune, L.E.9
Wagner Jr., H.N.10
Folstein, M.F.11
-
79
-
-
2642666489
-
Cognitive deficits in Huntington's disease are predicted by dopaminergic PET markers and brain volumes
-
Backman L Robins-Wahlin TB, Lundin A et al. Cognitive deficits in Huntington's disease are predicted by dopaminergic PET markers and brain volumes. Brain 1997; 120): 2207-2217
-
(1997)
Brain
, vol.120
, pp. 2207-2217
-
-
Backman, L.1
Robins-Wahlin, T.B.2
Lundin, A.3
-
80
-
-
0030897476
-
PET study of the pre- And post-synaptic dopaminergic markers for the neurodegenerative process in Huntington's disease
-
DOI 10.1093/brain/120.3.503
-
Ginovart N, Lundin A, Farde L et al. PET study of the pre- and postsynaptic dopaminergic markers for the neurodegenerative process in Huntington's disease. Brain 1997; 120: 503-514 (Pubitemid 27153642)
-
(1997)
Brain
, vol.120
, Issue.3
, pp. 503-514
-
-
Ginovart, N.1
Lundin, A.2
Farde, L.3
Halldin, C.4
Backman, L.5
Swahn, C.-G.6
Pauli, S.7
Sedvall, G.8
-
81
-
-
0031868226
-
The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's disease
-
Lawrence AD, Weeks RA, Brooks DJ et al. The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's disease. Brain 1998; 121: 1343-1355
-
(1998)
Brain
, vol.121
, pp. 1343-1355
-
-
Lawrence, A.D.1
Weeks, R.A.2
Brooks, D.J.3
-
82
-
-
41849133159
-
Cerebral cortex and the clinical expression of Huntington's disease: Complexity and heterogeneity
-
Rosas HD, Salat DH, Lee SY et al. Cerebral cortex and the clinical expression of Huntington's disease: complexity and heterogeneity. Brain 2008; 131: 1057-1068
-
(2008)
Brain
, vol.131
, pp. 1057-1068
-
-
Rosas, H.D.1
Salat, D.H.2
Lee, S.Y.3
-
83
-
-
53549112178
-
Altered frontostriatal coupling in pre-manifest Huntington's disease: Effects of increasing cognitive load
-
Wolf RC, Sambataro F, Vasic N et al. Altered frontostriatal coupling in pre-manifest Huntington's disease: effects of increasing cognitive load. Eur J Neurol 2008; 15: 1180-1190
-
(2008)
Eur J Neurol
, vol.15
, pp. 1180-1190
-
-
Wolf, R.C.1
Sambataro, F.2
Vasic, N.3
-
84
-
-
49349092621
-
Aberrant connectivity of lateral prefrontal networks in presymptomatic Huntington's disease
-
Wolf RC, Sambataro F, Vasic N et al. Aberrant connectivity of lateral prefrontal networks in presymptomatic Huntington's disease. Exp Neurol 2008; 213: 137-144
-
(2008)
Exp Neurol
, vol.213
, pp. 137-144
-
-
Wolf, R.C.1
Sambataro, F.2
Vasic, N.3
-
85
-
-
0029842587
-
Evidence of cortical metabolic dysfunction in early Huntington's disease by single -photon-emission computed tomography
-
DOI 10.1002/mds.870110612
-
Sax DS, Powsner R, Kim A et al. Evidence of cortical metabolic dysfunction in early Huntington's disease by single-photon-emission computed tomography. Mov Disord 1996; 11: 671-677 (Pubitemid 26381937)
-
(1996)
Movement Disorders
, vol.11
, Issue.6
, pp. 671-677
-
-
Sax, D.S.1
Powsner, R.2
Kim, A.3
Tilak, S.4
Bhatia, R.5
Cupples, L.A.6
Myers, R.H.7
-
86
-
-
35648966993
-
Dorsolateral prefrontal cortex dysfunction in presymptomatic Huntington's disease: Evidence from event-related fMRI
-
DOI 10.1093/brain/awm210
-
Wolf RC, Vasic N, Schonfeldt-Lecuona C et al. Dorsolateral prefrontal cortex dysfunction in presymptomatic Huntington's disease: evidence from event-related fMRI. Brain 2007; 130: 2845-2857 (Pubitemid 350033962)
-
(2007)
Brain
, vol.130
, Issue.11
, pp. 2845-2857
-
-
Wolf, R.C.1
Vasic, N.2
Schonfeldt-Lecuona, C.3
Landwehrmeyer, G.B.4
Ecker, D.5
-
87
-
-
62149136286
-
Functional imaging in Huntington's disease
-
Paulsen JS. Functional imaging in Huntington's disease. Exp Neurol 2009; 216: 272-277
-
(2009)
Exp Neurol
, vol.216
, pp. 272-277
-
-
Paulsen, J.S.1
-
88
-
-
0030935035
-
The likelihood of being affected with huntington disease by a particular age, for a specific CAG size
-
Brinkman RR, Mezei MM, Theilmann J et al. The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size. Am J Hum Genet 1997; 60: 1202-1210 (Pubitemid 27194105)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.5
, pp. 1202-1210
-
-
Brinkman, R.R.1
Mezei, M.M.2
Theilmann, J.3
Almqvist, E.4
Hayden, M.R.5
-
89
-
-
12144288251
-
Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset
-
DOI 10.1073/pnas.0308679101
-
Wexler NS, Lorimer J, Porter J et al. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. PNAS (USA) 2004; 101: 3498-3503 (Pubitemid 38338224)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.10
, pp. 3498-3503
-
-
Wexler, N.S.1
Lorimer, J.2
Porter, J.3
Gomez, F.4
Moskowitz, C.5
Shackell, E.6
Marder, K.7
Penchaszadeh, G.8
Roberts, S.A.9
Gayan, J.10
Brocklebank, D.11
Cherny, S.S.12
Cardon, L.R.13
Gray, J.14
Dlouhy, S.R.15
Wiktorski, S.16
Hodes, M.E.17
Conneally, P.M.18
Penney, J.B.19
Gusella, J.20
Cha, J.-H.21
Irizarry, M.22
Rosas, D.23
Hersch, S.24
Hollingsworth, Z.25
MacDonald, M.26
Young, A.B.27
Andresen, J.M.28
Housman, D.E.29
Mieja, D.30
Bonilla, E.31
Stillings, T.32
Negrette, A.33
Snodgrass, S.R.34
Martinez-Jaurrieta, M.D.35
Ramos-Arroyo, M.A.36
Bickham, J.37
Ramos, J.S.38
Marshall, F.39
Shoulson, I.40
Rey, G.J.41
Feigin, A.42
Arnheim, N.43
Acevedo-Cruz, A.44
Acosta, L.45
Alvir, J.46
Fischbeck, K.47
Thompson, L.M.48
Young, A.49
Dure, L.50
O'Brien, C.J.51
Paulsen, J.52
Brickman, A.53
Krch, D.54
Peery, S.55
Hogarth, P.56
Higgins Jr., D.S.57
Landwehrmeyeri, B.58
more..
-
90
-
-
1842477303
-
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length
-
Langbehn DR, Brinkman RR, Falush D et al. A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length. Clin Genet 2004; 65: 267-277
-
(2004)
Clin Genet
, vol.65
, pp. 267-277
-
-
Langbehn, D.R.1
Brinkman, R.R.2
Falush, D.3
-
91
-
-
0032860404
-
Reduced basal ganglia blood flow and volume in pre-symptomatic, gene-tested persons at-risk for Huntington's disease
-
Harris GJ, Codorl AM, Lewis RF et al. Reduced basal ganglia blood flow and volume in pre-symptomatic, gene-tested persons at-risk for Huntington's disease. Brain 1999; 122: 1667-1678
-
(1999)
Brain
, vol.122
, pp. 1667-1678
-
-
Harris, G.J.1
Codorl, A.M.2
Lewis, R.F.3
-
92
-
-
3242659833
-
Onset and rate of striatal atrophy in preclinical Huntington disease
-
Aylward EH, Sparks BF, Field KM et al. Onset and rate of striatal atrophy in preclinical Huntington disease. Neurology 2004; 63: 66-72
-
(2004)
Neurology
, vol.63
, pp. 66-72
-
-
Aylward, E.H.1
Sparks, B.F.2
Field, K.M.3
-
93
-
-
0029130324
-
Anticipation and instability of IT15 (CAG)n repeats in parent-offspring pairs with Huntington disease
-
Ranen NG, Stine OC, Abbott MH et al. Anticipation and instability of IT15 (CAG)n repeats in parent-offspring pairs with Huntington disease. AmJ Hum Genet 1995; 57: 593-602
-
(1995)
AmJ Hum Genet
, vol.57
, pp. 593-602
-
-
Ranen, N.G.1
Stine, O.C.2
Abbott, M.H.3
-
94
-
-
33846436448
-
Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds
-
DOI 10.1136/jmg.2006.045153
-
Andresen JM, Gayan J, Cherny SS et al. Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds. J Med Genet 2007; 44: 44-50 (Pubitemid 46142838)
-
(2007)
Journal of Medical Genetics
, vol.44
, Issue.1
, pp. 44-50
-
-
Andresen, J.M.1
Gayan, J.2
Cherny, S.S.3
Brocklebank, D.4
Alkorta-Aranburu, G.5
Addis, E.A.6
Cardon, L.R.7
Housman, D.E.8
Wexler, N.S.9
-
95
-
-
42449161835
-
ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease
-
Arning L Monte D, Hansen W et al. ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease. J Mol Med 2008; 86: 485-490
-
(2008)
J Mol Med
, vol.86
, pp. 485-490
-
-
Arningl, L.1
Monte, D.2
Hansen, W.3
-
96
-
-
15444363304
-
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease
-
DOI 10.1007/s10048-004-0198-8
-
Arning L Kraus PH, Valentin S et al. NR2A and NR2B receptor gene variations modify age at onset in Huntington disease. Neurogenetics 2005; 6: 25-28 (Pubitemid 40394827)
-
(2005)
Neurogenetics
, vol.6
, Issue.1
, pp. 25-28
-
-
Arning, L.1
Kraus, P.H.2
Valentin, S.3
Saft, C.4
Andrich, J.5
Epplen, J.T.6
-
97
-
-
34547735547
-
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner
-
DOI 10.1007/s00439-007-0393-4
-
Arning L, Saft C, Wieczorek S et al. NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner. Hum Gen 2007; 122: 175-182 (Pubitemid 47241782)
-
(2007)
Human Genetics
, vol.122
, Issue.2
, pp. 175-182
-
-
Arning, L.1
Saft, C.2
Wieczorek, S.3
Andrich, J.4
Kraus, P.H.5
Epplen, J.T.6
-
98
-
-
10044294013
-
Apolipoprotein e genotypes do not influence the age of onset in Huntington's disease
-
DOI 10.1136/jnnp.2003.022756
-
Saft C, Andrich JE, Brune N et al. Apolipoprotein E genotypes do not influence the age of onset in Huntington's disease. J Neurol Neurosurg Psychiatry 2004; 75: 1692-1696 (Pubitemid 39611467)
-
(2004)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.75
, Issue.12
, pp. 1692-1696
-
-
Saft, C.1
Andrich, J.E.2
Brune, N.3
Gencik, M.4
Kraus, P.H.5
Przuntek, H.6
Epplen, J.T.7
-
99
-
-
58649094617
-
The gene coding for PGC-lalpha modifies age at onset in Huntington's Disease
-
Weydt P, Soyal SM, Gellera C et al. The gene coding for PGC-lalpha modifies age at onset in Huntington's Disease. Mol Neurodegener 2009; 4: 3
-
(2009)
Mol Neurodegener
, vol.4
, pp. 3
-
-
Weydt, P.1
Soyal, S.M.2
Gellera, C.3
-
100
-
-
60849109499
-
PGC-lalpha as modifier of onset age in Huntington disease
-
Taherzadeh-Fard E, Saft C, Andrlch J et al. PGC-lalpha as modifier of onset age in Huntington disease. Mol Neurodegener 2009; 4: 10
-
(2009)
Mol Neurodegener
, vol.4
, pp. 10
-
-
Taherzadeh-Fard, E.1
Saft, C.2
Andrlch, J.3
-
101
-
-
0030919726
-
CAG repeat number governs the development rate of pathology in Huntington's disease
-
Penney JB Jr, Vonsattel JP, MacDonald ME et al. CAG repeat number governs the development rate of pathology in Huntington's disease. Ann Neurol 1997; 41: 689-692
-
(1997)
Ann Neurol
, vol.41
, pp. 689-692
-
-
Penney Jr., J.B.1
Vonsattel, J.P.2
MacDonald, M.E.3
-
103
-
-
52649139552
-
The relationship between CAG repeat length and clinical progression in Huntington's disease
-
Ravina B, Romer M, Constantlnescu R et al. The relationship between CAG repeat length and clinical progression in Huntington's disease. Mov Disord 2008; 23: 1223-1227
-
(2008)
Mov Disord
, vol.23
, pp. 1223-1227
-
-
Ravina, B.1
Romer, M.2
Constantlnescu, R.3
-
104
-
-
33646085784
-
The association of CAG repeat length with clinical progression in Huntington disease
-
Rosenbiatt A, Liang KY, Zhou H et al. The association of CAG repeat length with clinical progression in Huntington disease. Neurology 2006; 66: 1016-1020
-
(2006)
Neurology
, vol.66
, pp. 1016-1020
-
-
Rosenbiatt, A.1
Liang, K.Y.2
Zhou, H.3
-
105
-
-
0033432837
-
Pathophysiology of chorea and bradykinesia in Huntington's disease
-
Berardelli A, Noth J, Thompson PD et al. Pathophysiology of chorea and bradykinesia in Huntington's disease. Mov Disord 1999; 14: 398-403
-
(1999)
Mov Disord
, vol.14
, pp. 398-403
-
-
Berardelli, A.1
Noth, J.2
Thompson, P.D.3
-
106
-
-
0020664582
-
Absence of long latency reflexes to imposed finger displacements in patients with Huntington's disease
-
DOI 10.1016/0304-3940(83)90533-5
-
Noth J, Friedemann HH, Podoll K et al. Absence of long latency reflexes to imposed finger displacements in patients with Huntington's disease. Neurosci Lett 1983; 35: 97-100 (Pubitemid 13186958)
-
(1983)
Neuroscience Letters
, vol.35
, Issue.1
, pp. 97-100
-
-
Noth, J.1
Friedemann, H.H.2
Podoll, K.3
Lange, H.W.4
-
107
-
-
0021251389
-
Evoked potentials in patients with Huntington's disease and their offspring
-
Somatosensory evoked potentials.
-
Noth J, Engel L Friedemann HH et al. Evoked potentials in patients with Huntington's disease and their offspring. I. Somatosensory evoked potentials. Electroencephalogr Clin Neurophysiol 1984; 59: 134-141
-
(1984)
Electroencephalogr Clin Neurophysiol
, vol.1
, Issue.59
, pp. 134-141
-
-
Noth, J.1
Engel, L.2
Friedemann, H.H.3
-
108
-
-
0027388933
-
Comparison of somatosensory evoked potentials with striatal glucose consumption measured by positron emission tomography in the early diagnosis of Huntington's disease
-
DOI 10.1002/mds.870080118
-
Kuwert T, Noth J, Scholz D et al. Comparison of somatosensory evoked potentials with striatal glucose consumption measured by positron emission tomography in the early diagnosis of Huntington's disease. Mov Disord 1993; 8: 98-106 (Pubitemid 23039239)
-
(1993)
Movement Disorders
, vol.8
, Issue.1
, pp. 98-106
-
-
Kuwert, T.1
Noth, J.2
Scholz, D.3
Schwarz, M.4
Lange, H.W.5
Topper, R.6
Herzog, H.7
Aulich, A.8
Feinendegen, L.E.9
-
109
-
-
0017848944
-
The visually evoked potential in Huntington disease
-
Ellenberger C Jr, Petro DJ, Ziegler SB. The visually evoked potential in Huntington disease. Neurology 1978; 28: 95-97 (Pubitemid 8272525)
-
(1978)
Neurology
, vol.28
, Issue.1
, pp. 95-97
-
-
Ellenberger Jr., C.1
Petro, D.J.2
Ziegler, S.B.3
-
110
-
-
0021846558
-
Evoked potentials in patients with Huntington's disease and their offspring. II
-
Visual evoked potentials.
-
Hennerid M, Homberg V, Lange HW. Evoked potentials in patients with Huntington's disease and their offspring. II. Visual evoked potentials. Electroencephalogr Clin Neurophysiol 1985; 62: 167-176
-
(1985)
Electroencephalogr Clin Neurophysiol
, vol.62
, pp. 167-176
-
-
Hennerid, M.1
Homberg, V.2
Lange, H.W.3
-
111
-
-
0022642167
-
The diagnostic value of eye movement recordings in patients with Huntington's disease and their offspring
-
DOI 10.1016/0013-4694(86)90005-2
-
Beenen N, Buttner U, Lange HW. The diagnostic value of eye movement recordings in patients with Huntington's disease and their offspring. Electroencephalogr Clin Neurophysiol 1986; 63: 119-127 (Pubitemid 16154679)
-
(1986)
Electroencephalography and Clinical Neurophysiology
, vol.63
, Issue.2
, pp. 119-127
-
-
Beenen, N.1
Buttner, U.2
Lange, H.W.3
-
112
-
-
34548486951
-
Error processing in Huntington's disease
-
Beste C, Saft C, Andrlch J et al. Error processing in Huntington's disease. PLoS ONE 2006; 1: e86
-
(2006)
PLoS One
, vol.1
-
-
Beste, C.1
Saft, C.2
Andrlch, J.3
-
113
-
-
42749083644
-
Response inhibition in Huntington's disease - A study using ERPs and sLORETA
-
Beste C, Saft C, Andrlch J et al. Response inhibition in Huntington's disease - a study using ERPs and sLORETA. Neuropsychologia 2008; 46: 1290-1297
-
(2008)
Neuropsychologia
, vol.46
, pp. 1290-1297
-
-
Beste, C.1
Saft, C.2
Andrlch, J.3
-
114
-
-
44249121019
-
Time processing in Huntington's disease: A group-control study
-
Beste C, Saft C, Andrich J et al. Time processing in Huntington's disease: a group-control study. PLoS ONE 2007; 2: e1263
-
(2007)
PLoS ONE
, vol.2
-
-
Beste, C.1
Saft, C.2
Andrich, J.3
-
115
-
-
34548492007
-
Functional compensation or pathology in cortico-subcortical interactions in preclinical Huntington's disease?
-
Beste C, Saft C, YordanovaJ et al. Functional compensation or pathology in cortico-subcortical interactions in preclinical Huntington's disease? Neuropsychologia 2007; 45: 2922-2930
-
(2007)
Neuropsychologia
, vol.45
, pp. 2922-2930
-
-
Beste, C.1
Saft, C.2
Yordanova, J.3
-
116
-
-
58149232258
-
Increased cognitive functioning in symptomatic Huntington's disease as revealed by behavioral and event-related potential indices of auditory sensory memory and attention
-
Beste C, Saft C, Gunturkun O et al. Increased cognitive functioning in symptomatic Huntington's disease as revealed by behavioral and event-related potential indices of auditory sensory memory and attention. J Neurosci 2008; 28: 11695-11702
-
(2008)
J Neurosci
, vol.28
, pp. 11695-11702
-
-
Beste, C.1
Saft, C.2
Gunturkun, O.3
-
117
-
-
0023248782
-
Impairment of rapid movement in Huntington's disease
-
Hefter H, Homberg V, Lange HW et al. Impairment of rapid movement in Huntington's disease. Brain 1987; 110: 585-612 (Pubitemid 17081163)
-
(1987)
Brain
, vol.110
, Issue.3
, pp. 585-612
-
-
Hefter, H.1
Homberg, V.2
Lange, H.W.3
Freund, H.-J.4
-
118
-
-
0036223389
-
Bradykinesia in Huntington's disease. A prospective, follow-up study
-
DOI 10.1007/s004150200035
-
Garda Ruiz PJ, Hernandez J, Cantarero S et al. Bradykinesia in Huntington's disease. A prospective, follow-up study. J Neurol 2002; 249: 437-440 (Pubitemid 34304618)
-
(2002)
Journal of Neurology
, vol.249
, Issue.4
, pp. 437-440
-
-
Garcia, R.1
Ruiz, P.J.2
Hernandez, J.3
Cantarero, S.4
Bartolome, M.5
Sanchez, B.V.6
Garcia, D.7
-
119
-
-
3042578344
-
Objective assessment of motor slowness in Huntington's disease: Clinical correlates and 2-year follow-up
-
van Vugt JP, Piet KK, Vink LJ et al. Objective assessment of motor slowness in Huntington's disease: clinical correlates and 2-year follow-up. Mov Disord 2004; 19: 285-297
-
(2004)
Mov Disord
, vol.19
, pp. 285-297
-
-
Van Vugt, J.P.1
Piet, K.K.2
Vink, L.J.3
-
120
-
-
0035353731
-
Quantitative assessment of daytime motor activity provides a responsive measure of functional decline in patients with Huntington's disease
-
DOI 10.1002/mds.1097
-
van Vugt JP, Siesling S, Piet KK et al. Quantitative assessment of daytime motor activity provides a responsive measure of functional decline in patients with Huntington's disease. Mov Disord 2001; 16: 481-488 (Pubitemid 36041152)
-
(2001)
Movement Disorders
, vol.16
, Issue.3
, pp. 481-488
-
-
Van Vugt, J.P.1
Siesling, S.2
Piet, K.K.E.3
Zwinderman, A.H.4
Middelkoop, H.A.M.5
Roos, R.A.C.6
-
121
-
-
0035845618
-
Objective assessment of progression in huntington's disease: A 3-year follow-up study
-
Reilmann R, Kirsten F, Quinn L et al. Objective assessment of progression in Huntington's disease: a 3-year follow-up study. Neurology 2001; 57: 920-924 (Pubitemid 32845525)
-
(2001)
Neurology
, vol.57
, Issue.5
, pp. 920-924
-
-
Reilmann, R.1
Kirsten, F.2
Quinn, L.3
Henningsen, H.4
Marder, K.5
Gordon, A.M.6
-
122
-
-
26444489200
-
Reliability of spatiotemporal gait outcome measures in Huntington's disease
-
Rao AK, Quinn L Marder KS. Reliability of spatiotemporal gait outcome measures in Huntington's disease. Mov Disord 2005; 20: 1033-1037
-
(2005)
Mov Disord
, vol.20
, pp. 1033-1037
-
-
Rao, A.K.1
Quinn, L.2
Marder, K.S.3
-
123
-
-
1642553304
-
Assessment of complex movements reflects dysfunction in Huntington's disease
-
DOI 10.1007/s00415-003-0256-4
-
Saft C, Andrich J, Meisel NM et al. Assessment of complex movements reflects dysfunction in Huntington's disease. J Neurol 2003; 250: 1469-1474 (Pubitemid 38121845)
-
(2003)
Journal of Neurology
, vol.250
, Issue.12
, pp. 1469-1474
-
-
Saft, G.1
Andrich, J.2
Meisel, N.-M.3
Przuntek, H.4
Muller, T.5
-
124
-
-
33748350513
-
Assessment of simple movements reflects impairment in Huntington's disease
-
DOI 10.1002/mds.20939
-
Saft C, Andrich J, Meisel NM et al. Assessment of simple movements reflects impairment in Huntington's disease. Mov Disord 2006; 21: 1208-1212 (Pubitemid 44336609)
-
(2006)
Movement Disorders
, vol.21
, Issue.8
, pp. 1208-1212
-
-
Saft, C.1
Andrich, J.2
Meisel, N.-M.3
Przuntek, H.4
Muller, T.5
-
125
-
-
4544221197
-
Congruent deterioration of complex and simple movements in patients with Huntington's disease
-
Saft C, Andrich J, Meisel NM et al. Congruent deterioration of complex and simple movements in patients with Huntington's disease. J Neural Transm 2004; 68: 97-104 (Pubitemid 39215442)
-
(2004)
Journal of Neural Transmission, Supplement
, Issue.68
, pp. 97-104
-
-
Saft, C.1
Andrich, J.2
Meisel, N.-M.3
Przuntek, H.4
Muller, T.H.5
-
126
-
-
33947730591
-
Assessment of simple movements and progression of Huntington's disease
-
DOI 10.1136/jnnp.2006.105338
-
Andrich J, Saft C, Ostholt N et al. Assessment of simple movements and progression of Huntington's disease. J Neurol Neurosurg Psychiatry 2007; 78: 405-407 (Pubitemid 46580553)
-
(2007)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.78
, Issue.4
, pp. 405-407
-
-
Andrich, J.1
Saft, C.2
Ostholt, N.3
Muller, T.4
-
127
-
-
33947604998
-
Complex movement behaviour and progression of Huntington's disease
-
DOI 10.1016/j.neulet.2007.02.027, PII S0304394007001802
-
Andrich J, Saft C, Ostholt N et al. Complex movement behaviour and progression of Huntington's disease. Neurosci Lett 2007; 416: 272-274 (Pubitemid 46483870)
-
(2007)
Neuroscience Letters
, vol.416
, Issue.3
, pp. 272-274
-
-
Andrich, J.1
Saft, C.2
Ostholt, N.3
Muller, T.4
-
128
-
-
34250646632
-
Motor timing variability increases in preclinical Huntington's disease patients as estimated onset of motor symptoms approaches
-
Hinton SC, Paulsen JS, Hoffmann RG et al. Motor timing variability increases in preclinical Huntington's disease patients as estimated onset of motor symptoms approaches. J Int Neuropsychol Soc 2007; 13: 539-543
-
(2007)
J Int Neuropsychol Soc
, vol.13
, pp. 539-543
-
-
Hinton, S.C.1
Paulsen, J.S.2
Hoffmann, R.G.3
-
129
-
-
60049089806
-
Hand tapping: A simple, reproducible, objective marker of motor dysfunction in Huntington's disease
-
Michell AW, Goodman AO, Silva AH et al. Hand tapping: A simple, reproducible, objective marker of motor dysfunction in Huntington's disease. J Neurol 2008
-
(2008)
J Neurol
-
-
Michell, A.W.1
Goodman, A.O.2
Silva, A.H.3
-
131
-
-
0034598808
-
Motor disorder in Huntington's disease begins as a dysfunction in error feedback control
-
DOI 10.1038/35000576
-
Smith MA, Brandt J, Shadmehr R. Motor disorder in Huntington's disease begins as a dysfunction in error feedback control. Nature 2000; 403: 544-549 (Pubitemid 30082199)
-
(2000)
Nature
, vol.403
, Issue.6769
, pp. 544-549
-
-
Smith, M.A.1
Brandt, J.2
Shadmehr, R.3
-
132
-
-
33747037796
-
Saccades in presymptomatic and early stages of Huntington disease
-
Blekher T, Johnson SA, Marshall J et al. Saccades in presymptomatic and early stages of Huntington disease. Neurology 2006; 67: 394-399
-
(2006)
Neurology
, vol.67
, pp. 394-399
-
-
Blekher, T.1
Johnson, S.A.2
Marshall, J.3
-
133
-
-
49349101320
-
Oculomotor deficits indicate the progression of Huntington's disease
-
Hicks SL Robert MP, Golding CV et al. Oculomotor deficits indicate the progression of Huntington's disease. Prog Brain Res 2008; 171: 555-558
-
(2008)
Prog Brain Res
, vol.171
, pp. 555-558
-
-
Hicks, S.L.1
Robert, M.P.2
Golding, C.V.3
-
134
-
-
55849103175
-
Eye-head coordination in moderately affected Huntington's Disease patients: Do head movements facilitate gaze shifts?
-
Becker W, Jurgens R, KassubekJ et al. Eye-head coordination in moderately affected Huntington's Disease patients: do head movements facilitate gaze shifts? Exp Brain Res 2009; 192: 97-112
-
(2009)
Exp Brain Res
, vol.192
, pp. 97-112
-
-
Becker, W.1
Jurgens, R.2
Kassubek, J.3
-
135
-
-
33747074341
-
Predict-HD and the future of therapeutic trials
-
Wild EJ, Tabrizi SJ. Predict-HD and the future of therapeutic trials. Lancet Neurol 2006; 5: 724-725
-
(2006)
Lancet Neurol
, vol.5
, pp. 724-725
-
-
Wild, E.J.1
Tabrizi, S.J.2
-
136
-
-
0016704687
-
The Validity of Criteria for the Evaluation of Cerebral Atrophy by Computed Tomography
-
Huckman MS, Fox J, TopelJ. The validity of criteria for the evaluation of cerebral atrophy by computed tomography. Radiology 1975; 116: 85-92
-
(1975)
Radiology
, vol.116
, pp. 85-92
-
-
Huckman, M.S.1
Fox, J.2
Topel, J.3
-
137
-
-
0021325983
-
Bicaudate diameter - The most specific and simple CT parameter in the diagnosis of Huntington's disease
-
Stober T, Wussow W, Schimrigk K. Bicaudate diameter - the most specific and simple CT parameter in the diagnosis of Huntington's disease. Neuroradiology 1984; 26: 25-28 (Pubitemid 14211882)
-
(1984)
Neuroradiology
, vol.26
, Issue.1
, pp. 25-28
-
-
Stober, T.1
Wussow, W.2
Schimrigk, K.3
-
138
-
-
0030447557
-
Basal ganglia volume and proximity to onset in presymptomatic Huntington disease
-
Aylward EH, Codorl AM, Barta PE et al. Basal ganglia volume and proximity to onset in presymptomatic Huntington disease. Arch Neurol 1996; 53: 1293-1296
-
(1996)
Arch Neurol
, vol.53
, pp. 1293-1296
-
-
Aylward, E.H.1
Codorl, A.M.2
Barta, P.E.3
-
139
-
-
0034087487
-
Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease
-
Aylward EH, Codorl AM, Rosenblatt A et al. Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease. Mov Disord 2000; 15: 552-560
-
(2000)
Mov Disord
, vol.15
, pp. 552-560
-
-
Aylward, E.H.1
Codorl, A.M.2
Rosenblatt, A.3
-
140
-
-
0028365786
-
Reduced basal ganglia volume associated with the gene for Huntington's disease in asymptomatic at-risk persons
-
Aylward EH, Brandt J, Codorl AM et al. Reduced basal ganglia volume associated with the gene for Huntington's disease in asymptomatic at-risk persons. Neurology 1994; 44: 823-828
-
(1994)
Neurology
, vol.44
, pp. 823-828
-
-
Aylward, E.H.1
Brandt, J.2
Codorl, A.M.3
-
141
-
-
17644369971
-
Progression of structural neuropathology in preclinical Huntington's disease: A tensor based morphometry study
-
DOI 10.1136/jnnp.2004.047993
-
Kipps CM, Duggins AJ, Mahant N et al. Progression of structural neuropathology in preclinical Huntington's disease: a tensor based morphometry study. J Neurol Neurosurg Psychiatry 2005; 76: 650-655 (Pubitemid 40569674)
-
(2005)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.76
, Issue.5
, pp. 650-655
-
-
Kipps, C.M.1
Duggins, A.J.2
Mahant, N.3
Gomes, L.4
Ashburner, J.5
McCusker, E.A.6
-
142
-
-
0036345704
-
The distribution of structural neuropathology in pre-clinical Huntington's disease
-
Thieben MJ, Duggins AJ, Good CD et al. The distribution of structural neuropathology in pre-clinical Huntington's disease. Brain 2002; 125: 1815-1828
-
(2002)
Brain
, vol.125
, pp. 1815-1828
-
-
Thieben, M.J.1
Duggins, A.J.2
Good, C.D.3
-
143
-
-
24644479046
-
Regional cortical thinning in preclinical Huntington disease and its relationship to cognition
-
Rosas HD, Hevelone ND, Zaleta AK et al. Regional cortical thinning in preclinical Huntington disease and its relationship to cognition. Neurology 2005; 65: 745-747
-
(2005)
Neurology
, vol.65
, pp. 745-747
-
-
Rosas, H.D.1
Hevelone, N.D.2
Zaleta, A.K.3
-
144
-
-
34648827423
-
Morphology of the cerebral cortex in preclinical Huntington's disease
-
DOI 10.1176/appi.ajp.2007.06081266
-
Nopoulos P, Magnotta VA, Mikos A et al. Morphology of the cerebral cortex in preclinical Huntington's disease. Am J Psychiatry 2007; 164: 1428-1434 (Pubitemid 47461144)
-
(2007)
American Journal of Psychiatry
, vol.164
, Issue.9
, pp. 1428-1434
-
-
Nopoulos, P.1
Magnotta, V.A.2
Mikos, A.3
Paulson, H.4
Andreasen, N.C.5
Paulsen, J.S.6
-
146
-
-
33750358024
-
Diffusion tensor imaging in presymptomatic and early Huntington's disease: Selective white matter pathology and its relationship to clinical measures
-
Rosas HD, Tuch DS, Hevelone ND et al. Diffusion tensor imaging in presymptomatic and early Huntington's disease: Selective white matter pathology and its relationship to clinical measures. Mov Disord 2006; 21:1317-1325
-
(2006)
Mov Disord
, vol.21
, pp. 1317-1325
-
-
Rosas, H.D.1
Tuch, D.S.2
Hevelone, N.D.3
-
147
-
-
26644445690
-
Regional white matter change in pre-symptomatic Huntington's disease: A diffusion tensor imaging study
-
DOI 10.1016/j.pscychresns.2005.05.011, PII S092549270500106X
-
Reading SA, Yassa MA, Bakker A et al. Regional white matter change in pre-symptomatic Huntington's disease: a diffusion tensor imaging study. Psychiatry Res 2005; 140: 55-62 (Pubitemid 41443496)
-
(2005)
Psychiatry Research - Neuroimaging
, vol.140
, Issue.1
, pp. 55-62
-
-
Reading, S.A.J.1
Yassa, M.A.2
Bakker, A.3
Dziorny, A.C.4
Gourley, L.M.5
Yallapragada, V.6
Rosenblatt, A.7
Margolis, R.L.8
Aylward, E.H.9
Brandt, J.10
Mori, S.11
Van, Z.12
Bassett, S.S.13
Ross, C.A.14
-
148
-
-
37549063292
-
White matter connections reflect changes in voluntary-guided saccades in pre-symptomatic Huntington's disease
-
Kloppel S, Draganski B, Golding CVet al. White matter connections reflect changes in voluntary-guided saccades in pre-symptomatic Huntington's disease. Brain 2008; 131: 196-204
-
(2008)
Brain
, vol.131
, pp. 196-204
-
-
Kloppel, S.1
Draganski, B.2
Golding, C.V.3
-
149
-
-
61549122053
-
Automatic detection of preclinical neurodegeneration: Presymptomatic Huntington disease
-
Kloppel S, Chu C, Tan GC et al. Automatic detection of preclinical neurodegeneration: presymptomatic Huntington disease. Neurology 2009; 72: 426-431
-
(2009)
Neurology
, vol.72
, pp. 426-431
-
-
Kloppel, S.1
Chu, C.2
Tan, G.C.3
-
150
-
-
0031037349
-
Longitudinal change in basal ganglia volume in patients with Huntington's disease
-
Aylward EH, Li Q, Stine OC et al. Longitudinal change in basal ganglia volume in patients with Huntington's disease. Neurology 1997; 48: 394-399 (Pubitemid 27087610)
-
(1997)
Neurology
, vol.48
, Issue.2
, pp. 394-399
-
-
Aylward, E.H.1
Li, Q.2
Stine, O.C.3
Ranen, N.4
Sherr, M.5
Barta, P.E.6
Bylsma, F.W.7
Pearlson, G.D.8
Ross, C.A.9
-
151
-
-
0029563541
-
Impaired source memory in Huntington's disease and its relation to basal ganglia atrophy
-
Brandt J, Bylsma FW, Aylward EH et al. Impaired source memory in Huntington's disease and its relation to basal ganglia atrophy. J Clin Exp Neuropsychol 1995; 17: 868-877 (Pubitemid 26020988)
-
(1995)
Journal of Clinical and Experimental Neuropsychology
, vol.17
, Issue.6
, pp. 868-877
-
-
Brandt, J.1
Bylsma, F.W.2
Aylward, E.H.3
Rothlind, J.4
Gow, C.A.5
-
152
-
-
0026584454
-
Magnetic resonance imaging exceeds caudate changes in mild Huntington's disease
-
Harris GJ, Pearlson GD, Peyser CE et al. Putamen volume reduction on magnetic resonance imaging exceeds caudate changes in mild Huntington's disease. Ann Neurol 1992; 31: 69-75
-
(1992)
Ann Neurol
, vol.31
, pp. 69-75
-
-
Harris, G.J.1
Pearlson, G.D.2
Peyser, C.E.3
On, E.A.P.V.R.4
-
153
-
-
0038476184
-
Evidence for more widespread cerebral pathology in early HD: An MRI-based morphometric analysis
-
Rosas HD, Koroshetz WJ, Chen YI et al. Evidence for more widespread cerebral pathology in early HD: an MRI-based morphometric analysis. Neurology 2003; 60: 1615-1620
-
(2003)
Neurology
, vol.60
, pp. 1615-1620
-
-
Rosas, H.D.1
Koroshetz, W.J.2
Chen, Y.I.3
-
154
-
-
33747378753
-
Striatal and extrastriatal atrophy in Huntington's disease and its relationship with length of the CAG repeat
-
Ruocco HH, Lopes-Cendes I, Li LM et al. Striatal and extrastriatal atrophy in Huntington's disease and its relationship with length of the CAG repeat. Brazilian Journal of Medical and Biological Research-Revista brasileira de pesquisas medicas e biologicas / Sociedade Brasileira de Biofisica [et al] 2006; 39: 1129-1136 (Pubitemid 44241274)
-
(2006)
Brazilian Journal of Medical and Biological Research
, vol.39
, Issue.8
, pp. 1129-1136
-
-
Ruocco, H.H.1
Lopes-Cendes, I.2
Li, L.M.3
Santos-Silva, M.4
Cendes, F.5
-
155
-
-
0026714774
-
Neuropsychological correlates of brain atrophy in Huntington's disease: A magnetic resonance imaging study
-
Starkstein SE, Brandt J, Bylsma F et al. Neuropsychological correlates of brain atrophy in Huntington's disease: a magnetic resonance imaging study. Neuroradiology 1992; 34: 487-489
-
(1992)
Neuroradiology
, vol.34
, pp. 487-489
-
-
Starkstein, S.E.1
Brandt, J.2
Bylsma, F.3
-
156
-
-
45549085845
-
Magnetic resonance imaging as an approach towards identifying neuropathological biomarkers for Huntington's disease
-
Bohanna I, Georgiou-Karistianis N, Hannan AJ et al. Magnetic resonance imaging as an approach towards identifying neuropathological biomarkers for Huntington's disease. Brain Res Rev 2008
-
(2008)
Brain Res Rev
-
-
Bohanna, I.1
Georgiou-Karistianis, N.2
Hannan, A.J.3
-
157
-
-
33847297059
-
Voxel-based morphometry indicates relative preservation of the limbic prefrontal cortex in early Huntington disease
-
DOI 10.1007/s00702-006-0571-x
-
Muhlau M, Weindi A, Wohlschlager AM et al. Voxel-based morphometry indicates relative preservation of the limbic prefrontal cortex in early Huntington disease. J Neural Transm 2007; 114: 367-372 (Pubitemid 46328656)
-
(2007)
Journal of Neural Transmission
, vol.114
, Issue.3
, pp. 367-372
-
-
Muhlau, M.1
Weindl, A.2
Wohlschlager, A.M.3
Gaser, C.4
Stadtler, M.5
Valet, M.6
Zimmer, C.7
Kassubek, J.8
Peinemann, A.9
-
158
-
-
4143085873
-
Huntington disease: Volumetric, diffusion-weighted, and magnetization transfer MR imaging of brain
-
Mascalchi M, Lolli F, Della Nave R et al. Huntington disease: volumetric, diffusion-weighted, and magnetization transfer MR imaging of brain. Radiology 2004; 232: 867-873
-
(2004)
Radiology
, Issue.232
, pp. 867-873
-
-
Mascalchi, M.1
Lolli, F.2
Della Nave, R.3
-
159
-
-
35348940660
-
Variation of selective gray and white matter atrophy in Huntington's disease
-
DOI 10.1002/mds.21620
-
Jech R, Klempir J, Vymazal J et al. Variation of selective gray and white matter atrophy in Huntington's disease. Mov Disord 2007; 22: 1783-1789 (Pubitemid 47597603)
-
(2007)
Movement Disorders
, vol.22
, Issue.12
, pp. 1783-1789
-
-
Jech, R.1
Klempir, J.2
Vymazal, J.3
Zidovska, J.4
Klempirova, O.5
Ruzicka, E.6
Roth, J.7
-
161
-
-
10744221516
-
Topography of cerebral atrophy in early Huntington's disease: A voxel based morphometric MRI study
-
Kassubek J, Juengling FD, Kioschies T et al. Topography of cerebral atrophy in early Huntington's disease: a voxel based morphometric MRI study. J Neurol Neurosurg Psychiatry 2004; 75: 213-220 (Pubitemid 38183526)
-
(2004)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.75
, Issue.2
, pp. 213-220
-
-
Kassubek, J.1
Juengling, F.D.2
Kioschies, T.3
Henkel, K.4
Karitzky, J.5
Kramer, B.6
Ecker, D.7
Andrich, J.8
Saft, C.9
Kraus, P.10
Aschoff, A.J.11
Ludolph, A.C.12
Landwehrmeyer, G.B.13
-
162
-
-
33748302789
-
Distribution of grey matter atrophy in Huntington's disease patients: A combined ROI-based and voxel-based morphometric study
-
DOI 10.1016/j.neuroimage.2006.05.057, PII S1053811906006422
-
Douaud G, Gaura V, Ribeiro MJ et al. Distribution of grey matter atrophy in Huntington's disease patients: a combined ROI-based and voxel-based morphometric study. Neurolmage 2006; 32: 1562-1575 (Pubitemid 44332291)
-
(2006)
NeuroImage
, vol.32
, Issue.4
, pp. 1562-1575
-
-
Douaud, G.1
Gaura, V.2
Ribeiro, M.-J.3
Lethimonnier, F.4
Maroy, R.5
Verny, C.6
Krystkowiak, P.7
Damier, P.8
Bachoud-Levi, A.-C.9
Hantraye, P.10
Remy, P.11
-
163
-
-
64649101181
-
Voxel-based morphometry in individual patients: A pilot study in early Huntington disease
-
Muhlau M, Wohlschlager AM, Gaser Cet al. Voxel-based morphometry in individual patients: a pilot study in early Huntington disease. Ajnr 2009; 30: 539-543
-
(2009)
Ajnr
, vol.30
, pp. 539-543
-
-
Muhlau, M.1
Wohlschlager, A.M.2
Gaser, C.3
-
164
-
-
67349234997
-
In vivo evidence for the selective subcortical degeneration in Huntington's disease
-
Douaud G, Behrens TE, Poupon Cet al. In vivo evidence for the selective subcortical degeneration in Huntington's disease. Neurolmage 2009; 46: 958-966
-
(2009)
Neurolmage
, vol.46
, pp. 958-966
-
-
Douaud, G.1
Behrens, T.E.2
Poupon, C.3
-
165
-
-
33747682833
-
Atrophy over 6 months in early Huntington disease
-
Henley SM, Frost C, MacManus DG et al. Increased rate of whole-brain atrophy over 6 months in early Huntington disease. Neurology 2006; 67: 694-696
-
(2006)
Neurology
, vol.67
, pp. 694-696
-
-
Henley, S.M.1
Frost, C.2
MacManus, D.G.3
-
166
-
-
67651162162
-
Whole-brain atrophy as a measure of progression in premanifest and early Huntington's disease
-
Henley SM, Wild EJ, Hobbs NZ et al. Whole-brain atrophy as a measure of progression in premanifest and early Huntington's disease. Mov Disord 2009; 24: 932-936
-
(2009)
Mov Disord
, vol.24
, pp. 932-936
-
-
Henley, S.M.1
Wild, E.J.2
Hobbs, N.Z.3
-
167
-
-
1542320248
-
Global cerebral atrophy in early stages of Huntington's disease: Quantitative MRI study
-
KassubekJ, Landwehrmeyer GB, Ecker D et al. Global cerebral atrophy in early stages of Huntington's disease: quantitative MRI study. Neuroreport 2004; 15: 363-365
-
(2004)
Neuroreport
, vol.15
, pp. 363-365
-
-
Kassubek, J.1
Landwehrmeyer, G.B.2
Ecker, D.3
-
168
-
-
34447559713
-
Striatal gray matter loss in Huntington's disease is leftward biased
-
Muhlau M, Gaser C, Wohlschlager AM et al. Striatal gray matter loss in Huntington's disease is leftward biased. Mov Disord 2007; 22:1169-1173
-
(2007)
Mov Disord
, vol.22
, pp. 1169-1173
-
-
Muhlau, M.1
Gaser, C.2
Wohlschlager, A.M.3
-
169
-
-
0032424883
-
Regional specificity of brain atrophy in Huntington's disease
-
Halliday GM, McRitchie DA, Macdonald V et al. Regional specificity of brain atrophy in Huntington's disease. Exp Neurol 1998; 154: 663-672
-
(1998)
Exp Neurol
, vol.154
, pp. 663-672
-
-
Halliday, G.M.1
McRitchie, D.A.2
Macdonald, V.3
-
170
-
-
0037066115
-
Regional and progressive thinning of the cortical ribbon in Huntington's disease
-
Rosas HD, Liu AK, Hersch S et al. Regional and progressive thinning of the cortical ribbon in Huntington's disease. Neurology 2002; 58: 695-701 (Pubitemid 34211546)
-
(2002)
Neurology
, vol.58
, Issue.5
, pp. 695-701
-
-
Rosas, H.D.1
Liu, A.K.2
Hersch, S.3
Glessner, M.4
Ferrante, R.J.5
Salat, D.H.6
Van, D.7
Jenkins, B.G.8
Dale, A.M.9
Fischl, B.10
-
171
-
-
33746904273
-
Diffusion-weighted imaging in Huntington's disease
-
Seppl K, Schocke MF, Mair KJ et al. Diffusion-weighted imaging in Huntington's disease. Mov Disord 2006; 21: 1043-1047
-
(2006)
Mov Disord
, vol.21
, pp. 1043-1047
-
-
Seppl, K.1
Schocke, M.F.2
Mair, K.J.3
-
172
-
-
62049085680
-
Longitudinal diffusion tensor imaging in Huntington's Disease
-
Weaver KE, Richards TL Liang O et al. Longitudinal diffusion tensor imaging in Huntington's Disease. Exp Neurol 2009; 216: 525-529
-
(2009)
Exp Neurol
, vol.216
, pp. 525-529
-
-
Weaver, K.E.1
Richards, T.L.2
Liang, O.3
-
173
-
-
62149090287
-
Diffusion-weighted versus volumetric imaging of the striatum in early symptomatic Huntington disease
-
Vandenberghe W, Demaerel P, Dom R et al. Diffusion-weighted versus volumetric imaging of the striatum in early symptomatic Huntington disease. J Neurol 2009; 256: 109-114
-
(2009)
J Neurol
, Issue.256
, pp. 109-114
-
-
Vandenberghe, W.1
Demaerel, P.2
Dom, R.3
-
174
-
-
0022930826
-
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
-
Alexander GE, DeLong MR, Strick PL Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Ann Rev Neurosci 1986; 9: 357-381
-
(1986)
Ann Rev Neurosci
, vol.9
, pp. 357-381
-
-
Alexander, G.E.1
Delong, M.R.2
Strick, P.L.3
-
175
-
-
0034571171
-
Huntington's disease: The challenge for cell biologists
-
Tobin AJ, Signer ER. Huntington's disease: the challenge for cell biologists. Trends Cell Biol 2000; 10: 531-536
-
(2000)
Trends Cell Biol
, vol.10
, pp. 531-536
-
-
Tobin, A.J.1
Signer, E.R.2
-
176
-
-
0029943742
-
Proton magnetic resonance spectroscopy in Huntington's disease: Evidence in favour of the glutamate excitotoxic theory
-
Taylor-Robinson SD, Weeks RA, Bryant DJ et al. Proton magnetic resonance spectroscopy in Huntington's disease: evidence in favour of the glutamate excitotoxic theory. Mov Disord 1996; 11: 167-173
-
(1996)
Mov Disord
, vol.11
, pp. 167-173
-
-
Taylor-Robinson, S.D.1
Weeks, R.A.2
Bryant, D.J.3
-
177
-
-
0031596998
-
IH NMR spectroscopy studies of Huntington's disease: Correlations with CAG repeat numbers
-
Jenkins BG, Rosas HD, Chen YC et al. IH NMR spectroscopy studies of Huntington's disease: correlations with CAG repeat numbers. Neurology 1998; 50: 1357-1365
-
(1998)
Neurology
, vol.50
, pp. 1357-1365
-
-
Jenkins, B.G.1
Rosas, H.D.2
Chen, Y.C.3
-
178
-
-
35649013819
-
Is brain lactate increased in Huntington's disease?
-
Martin WR, Wieler M, Hanstock CC. Is brain lactate increased in Huntington's disease? J Neurol Sci 2007; 263: 70-74
-
(2007)
J Neurol Sci
, vol.263
, pp. 70-74
-
-
Martin, W.R.1
Wieler, M.2
Hanstock, C.C.3
-
179
-
-
0031035154
-
Decreased N-acetyl-aspartate/choline ratio and increased lactate in the frontal lobe of patients with Huntington's disease: A proton magnetic resonance spectroscopy study
-
Harms L, Meierkord H, Timm G et al. Decreased N-acetyl-aspartate/ choline ratio and increased lactate in the frontal lobe of patients with Huntington's disease: a proton magnetic resonance spectroscopy study. J Neurol Neurosurg Psychiatry 1997; 62: 27-30 (Pubitemid 27047437)
-
(1997)
Journal of Neurology Neurosurgery and Psychiatry
, vol.62
, Issue.1
, pp. 27-30
-
-
Harms, L.1
Meierkord, H.2
Timm, G.3
Pfeiffer, L.4
Ludolph, A.C.5
-
180
-
-
0031900412
-
Quantitative proton-decoupled 31P MRS and IH MRS in the evaluation of Huntington's and Parkinson's diseases
-
Hoang TQ, Bluml S, Dubowitz DJ et al. Quantitative proton-decoupled 31P MRS and IH MRS in the evaluation of Huntington's and Parkinson's diseases. Neurology 1998; 50: 1033-1040
-
(1998)
Neurology
, vol.50
, pp. 1033-1040
-
-
Hoang, T.Q.1
Bluml, S.2
Dubowitz, D.J.3
-
181
-
-
0033546998
-
Clinical correlation of striatal IH MRS changes in Huntington's disease
-
Sanchez-Pernaute R, Garcia-Segura JM, del Barrio Alba A et al. Clinical correlation of striatal IH MRS changes in Huntington's disease. Neurology 1999; 53: 806-812
-
(1999)
Neurology
, vol.53
, pp. 806-812
-
-
Sanchez-Pernaute, R.1
Garcia-Segura, J.M.2
Del Barrio, A.A.3
-
182
-
-
19944431628
-
Creatine supplementation lowers brain glutamate levels in Huntington's disease
-
DOI 10.1007/s00415-005-0595-4
-
Bender A, Auer DP, Merl T et al. Creatine supplementation lowers brain glutamate levels in Huntington's disease. J Neurol 2005; 252: 36-41 (Pubitemid 40179016)
-
(2005)
Journal of Neurology
, vol.252
, Issue.1
, pp. 36-41
-
-
Bender, A.1
Auer, D.P.2
Merl, T.3
Reilmann, R.4
Saemann, P.5
Yassouridis, A.6
Bender, J.7
Weindl, A.8
Dose, M.9
Gasser, T.10
Klopstock, T.11
-
183
-
-
18144370445
-
High-dose creatine therapy for Huntington disease: A 2-year clinical and MRS study
-
Tabrizi SJ, Blamire AM, Manners DN et al. High-dose creatine therapy for Huntington disease: a 2-year clinical and MRS study. Neurology 2005; 64: 1655-1656
-
(2005)
Neurology
, vol.64
, pp. 1655-1656
-
-
Tabrizi, S.J.1
Blamire, A.M.2
Manners, D.N.3
-
184
-
-
0037677341
-
Creatine therapy for Huntington's disease: Clinical and MRS findings in a 1-year pilot study
-
Tabrizi SJ, Blamire AM, Manners DN et al. Creatine therapy for Huntington's disease: clinical and MRS findings in a 1-year pilot study. Neurology 2003; 61: 141-142
-
(2003)
Neurology
, vol.61
, pp. 141-142
-
-
Tabrizi, S.J.1
Blamire, A.M.2
Manners, D.N.3
-
185
-
-
11144291556
-
Heterogeneity in IH-MRS profiles of presymptomatic and early manifest Huntington's disease
-
Reynolds NC Jr, Prost RW, Mark LP. Heterogeneity in IH-MRS profiles of presymptomatic and early manifest Huntington's disease. Brain Res 2005; 1031: 82-89
-
(2005)
Brain Res
, vol.1031
, pp. 82-89
-
-
Reynolds Jr., N.C.1
Prost, R.W.2
Mark, L.P.3
-
186
-
-
0033914747
-
Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy
-
DOI 10.1002/1531-8249(200007)48:1<72::AID-ANA11>3.0.CO;2-I
-
Lodi R, Schapira AH, Manners Detal. Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy. Ann Neurol 2000; 48: 72-76 (Pubitemid 30432433)
-
(2000)
Annals of Neurology
, vol.48
, Issue.1
, pp. 72-76
-
-
Lodi, R.1
Schapira, A.H.V.2
Manners, D.3
Styles, P.4
Wood, N.W.5
Taylor, D.J.6
Warner, T.T.7
-
187
-
-
22844440902
-
Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease
-
DOI 10.1002/mds.20373
-
Saft C, Zange J, Andrich J et al. Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease. Mov Disord 2005; 20: 674-679 (Pubitemid 41051778)
-
(2005)
Movement Disorders
, vol.20
, Issue.6
, pp. 674-679
-
-
Saft, C.1
Zange, J.2
Andrich, J.3
Muller, K.4
Lindenberg, K.5
Landwehrmeyer, B.6
Vorgerd, M.7
Kraus, P.H.8
Przuntek, H.9
Schols, L.10
-
188
-
-
34548275049
-
1H magnetic resonance spectroscopy in preclinical Huntington disease
-
DOI 10.1016/j.brainres.2007.05.082, PII S0006899307013571
-
van Oostrom JC, Sijens PE, Roos RA et al. 1H magnetic resonance spectroscopy in preclinical Huntington disease. Brain Res 2007; 1168: 67-71 (Pubitemid 47320622)
-
(2007)
Brain Research
, vol.1168
, Issue.1
, pp. 67-71
-
-
Van Oostrom, J.C.1
Sijens, P.E.2
Roos, R.A.C.3
Leenders, K.L.4
-
189
-
-
2942615264
-
Neural correlates associated with impaired disgust processing in pre-symptomatic Huntington's disease
-
Hennenlotter A, Schroeder U, Erhard P et al. Neural correlates associated with impaired disgust processing in pre-symptomatic Huntington's disease. Brain 2004; 127: 1446-1453
-
(2004)
Brain
, vol.127
, pp. 1446-1453
-
-
Hennenlotter, A.1
Schroeder, U.2
Erhard, P.3
-
190
-
-
0029966943
-
Loss of disgust. Perception of faces and emotions in Huntington's disease
-
Sprengelmeyer R, YoungAW, Calder AJ et al. Loss of disgust. Perception of faces and emotions in Huntington's disease. Brain 1996; 119: 147-1665
-
(1996)
Brain
, vol.119
, pp. 147-1665
-
-
Sprengelmeyer, R.1
Youngaw, A.W.2
Calder, A.J.3
-
191
-
-
2542627541
-
Functional brain changes in presymptomatic Huntington's disease
-
Reading SA, DziornyAC, Peroutka LA et al. Functional brain changes in presymptomatic Huntington's disease. Ann Neurol 2004; 55: 879-883
-
(2004)
Ann Neurol
, vol.55
, pp. 879-883
-
-
Reading, S.A.1
Dziornyac, A.C.2
Peroutka, L.A.3
-
192
-
-
16644395282
-
FMRI biomarker of early neuronal dysfunction in presymptomatic Huntington's disease
-
Paulsen JS, Zimbelman JL Hinton SC et al. fMRI biomarker of early neuronal dysfunction in presymptomatic Huntington's disease. AJNR 2004; 25: 1715-1721
-
(2004)
AJNR
, vol.25
, pp. 1715-1721
-
-
Paulsen, J.S.1
Hinton, S.C.2
Zimbelman, J.L.3
-
193
-
-
34548131996
-
FMRI detection of early neural dysfunction in preclinical Huntington's disease
-
DOI 10.1017/S1355617707071214, PII S1355617707071214
-
Zimbelman JL Paulsen JS, Mikos A et al. fMRI detection of early neural dysfunction in preclinical Huntington's disease. J Int Neuropsychol Soc 2007; 13: 758-769 (Pubitemid 47299445)
-
(2007)
Journal of the International Neuropsychological Society
, vol.13
, Issue.5
, pp. 758-769
-
-
Zimbelman, J.L.1
Paulsen, J.S.2
Mikos, A.3
Reynolds, N.C.4
Hoffmann, R.G.5
Rao, S.M.6
-
194
-
-
42749093219
-
FMRI reveals altered auditory processing in manifest and premanifest Huntington's disease
-
Saft C, Schuttke A, Beste C et al. fMRI reveals altered auditory processing in manifest and premanifest Huntington's disease. Neuropsychologia 2008; 46: 1279-1289
-
(2008)
Neuropsychologia
, vol.46
, pp. 1279-1289
-
-
Saft, C.1
Schuttke, A.2
Beste, C.3
-
195
-
-
0344643407
-
Inhibition of subliminally primed responses is mediated by the caudate and thalamus: Evidence from functional MRI and Huntington's disease
-
DOI 10.1093/brain/awg067
-
Aron AR, Schlaghecken F, Fletcher PC et al. Inhibition of subliminally primed responses is mediated by the caudate and thalamus: evidence from functional MRI and Huntington's disease. Brain 2003; 126: 713-723 (Pubitemid 36240871)
-
(2003)
Brain
, vol.126
, Issue.3
, pp. 713-723
-
-
Aron, A.R.1
Schlaghecken, F.2
Fletcher, P.C.3
Bullmore, E.T.4
Eimer, M.5
Barker, R.6
Sahakian, B.J.7
Robbins, T.W.8
-
196
-
-
4043112756
-
Interaction between the human hippocampus and the caudate nucleus during route recognition
-
Voermans NC, Petersson KM, Daudey L et al. Interaction between the human hippocampus and the caudate nucleus during route recognition. Neuron 2004; 43: 427-435
-
(2004)
Neuron
, vol.43
, pp. 427-435
-
-
Voermans, N.C.1
Petersson, K.M.2
Daudey, L.3
-
197
-
-
34648812766
-
Combining functional and structural brain magnetic resonance imaging in Huntington disease
-
DOI 10.1097/01.rct.0000284390.53202.2e, PII 0000472820070700000015
-
Gavazzi C, Nave RD, Petralli R et al. Combining functional and structural brain magnetic resonance imaging in Huntington disease. J Cornput Assist Tomogr 2007; 31: 574-580 (Pubitemid 47457673)
-
(2007)
Journal of Computer Assisted Tomography
, vol.31
, Issue.4
, pp. 574-580
-
-
Gavazzi, C.1
Nave, R.D.2
Petralli, R.3
Rocca, M.A.4
Guerrini, L.5
Tessa, C.6
Diciotti, S.7
Filippi, M.8
Piacentini, S.9
Mascalchi, M.10
-
198
-
-
0033593670
-
Multimodal imaging of residual function and compensatory resource allocation in cortical atrophy: A case study of parietal lobe function in a patient with Huntington's disease
-
Dierks T, Linden DE, Hertel A et al. Multimodal imaging of residual function and compensatory resource allocation in cortical atrophy: a case study of parietal lobe function in a patient with Huntington's disease. Psychiatry Res 1999; 90: 67-75
-
(1999)
Psychiatry Res
, vol.90
, pp. 67-75
-
-
Dierks, T.1
Linden, D.E.2
Hertel, A.3
-
199
-
-
33847727473
-
Increased cortical recruitment in Huntington's disease using a Simon task
-
Georgiou-Karistianis N, Sritharan A, Farrow M et al. Increased cortical recruitment in Huntington's disease using a Simon task. Neuropsychologia 2007; 45: 1791-1800
-
(2007)
Neuropsychologia
, vol.45
, pp. 1791-1800
-
-
Georgiou-Karistianis, N.1
Sritharan, A.2
Farrow, M.3
-
200
-
-
0037117731
-
Altered functional MRI responses in Huntington's disease
-
Clark VP, Lai S, Deckel AW. Altered functional MRI responses in Huntington's disease. Neuroreport 2002; 13:703-706 (Pubitemid 34293495)
-
(2002)
NeuroReport
, vol.13
, Issue.5
, pp. 703-706
-
-
Clark, V.P.1
Lai, S.2
Deckel, A.W.3
-
201
-
-
3042832791
-
Functional MRI study of a serial reaction time task in Huntington's disease
-
Kim JS, Reading SA, Brashers-Krug T et al. Functional MRI study of a serial reaction time task in Huntington's disease. Psychiatry Res 2004; 131: 23-30
-
(2004)
Psychiatry Res
, vol.131
, pp. 23-30
-
-
Kim, J.S.1
Reading, S.A.2
Brashers-Krug, T.3
-
202
-
-
33846891069
-
Functional connectivity of the prefrontal cortex in Huntington's disease
-
DOI 10.1136/jnnp.2006.098368
-
Thiruvady DR, Georglou-Karlstlanls N, Egan GF et al. Functional connectivity of the prefrontal cortex in Huntington's disease. J Neurol Neurosurg Psychiatry 2007; 78: 127-133 (Pubitemid 46220207)
-
(2007)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.78
, Issue.2
, pp. 127-133
-
-
Thiruvady, D.R.1
Georgiou-Karistianis, N.2
Egan, G.F.3
Ray, S.4
Sritharan, A.5
Farrow, M.6
Churchyard, A.7
Chua, P.8
Bradshaw, J.L.9
Brawn, T.-L.10
Cunnington, R.11
-
203
-
-
65549118710
-
Functional Connectivity during auditory processing in Huntington's disease
-
Beste C, Schuttke A, Konrád C et al. Functional Connectivity during auditory processing in Huntington's disease. J Psychphysiol 2008; 22: 195-201
-
(2008)
J Psychphysiol
, vol.22
, pp. 195-201
-
-
Beste, C.1
Schuttke, A.2
Konrád, C.3
-
204
-
-
72449181276
-
Altered auditory sensory processing in premanifest Huntington's disease: Are there different phases in premanifest Huntington's disease?
-
All
-
Saft C, Schutte A, Beste C et al. Altered auditory sensory processing in premanifest Huntington's disease: Are there different phases in premanifest Huntington's disease? J Neurol Neurosurg Psychiatry 2008; 79: All
-
(2008)
J Neurol Neurosurg Psychiatry
, vol.79
-
-
Saft, C.1
Schutte, A.2
Beste, C.3
-
205
-
-
0019991784
-
Cerebral metabolism and atrophy in Huntington's disease determined by 18FDG and computed tomographic scan
-
Kuhi DE, Phelps ME, Markham CH et al. Cerebral metabolism and atrophy in Huntington's disease determined by 18FDG and computed tomographic scan. Ann Neurol 1982; 12: 425-434
-
(1982)
Ann Neurol
, vol.12
, pp. 425-434
-
-
Kuhi, D.E.1
Phelps, M.E.2
Markham, C.H.3
-
206
-
-
0026788036
-
Influence of size of regions of interest on PET evaluation of caudate glucose consumption
-
Kuwert T, Ganslandt T, Jansen P et al. Influence of size of regions of interest on PET evaluation of caudate glucose consumption. J Comput Assist Tomogr 1992; 16: 789-794
-
(1992)
J Comput Assist Tomogr
, vol.16
, pp. 789-794
-
-
Kuwert, T.1
Ganslandt, T.2
Jansen, P.3
-
207
-
-
0027441163
-
Striatal glucose consumption in chorea-free subjects at risk of Huntington's disease
-
DOI 10.1007/BF00870669
-
Kuwert T, Lange HW, Boecker H et al. Striatal glucose consumption in chorea-free subjects at risk of Huntington's disease. J Neurol 1993; 241: 31-36 (Pubitemid 23342424)
-
(1993)
Journal of Neurology
, vol.241
, Issue.1
, pp. 31-36
-
-
Kuwert, T.1
Lange, H.W.2
Boecker, H.3
Titz, H.4
Herzog, H.5
Aulich, A.6
Wang, B.C.7
Nayak, U.8
Feinendegen, L.E.9
-
208
-
-
0022553413
-
PET scan investigations of Huntington's disease: Cerebral metabolic correlates of neurological features and functional decline
-
Young AB, Penney JB, Starosta-Rubinstein S et al. PET scan investigations of Huntington's disease: cerebral metabolic correlates of neurological features and functional decline. Ann Neurol 1986; 20: 296-303 (Pubitemid 16018512)
-
(1986)
Annals of Neurology
, vol.20
, Issue.3
, pp. 296-303
-
-
Young, A.B.1
Penney, J.B.2
Starosta-Rubinstein, S.3
-
209
-
-
0023098788
-
Normal caudate glucose metabolism in persons at risk for Huntington's disease
-
Young AB, Penney JB, Starosta-Rubinstein S et al. Normal caudate glucose metabolism in persons at risk for Huntington's disease. Arch Neurol 1987; 44: 254-257
-
(1987)
Arch Neurol
, vol.44
, pp. 254-257
-
-
Young, A.B.1
Penney, J.B.2
Starosta-Rubinstein, S.3
-
210
-
-
0026475301
-
Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's disease
-
Grafton ST, Mazziotta JC, Pahl JJ et al. Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's disease. Arch Neurol 1992; 49: 1161-1167
-
(1992)
Arch Neurol
, vol.49
, pp. 1161-1167
-
-
Grafton, S.T.1
Mazziotta, J.C.2
Pahl, J.J.3
-
211
-
-
0023146627
-
Dopamine receptor properties in Parkinson's disease and Huntington's chorea evaluated by positron emission tomography using 11 C-N-methyl-spiperone
-
Hagglund J, Aqullonius SM, Eckernas SA et al. Dopamine receptor properties in Parkinson's disease and Huntington's chorea evaluated by positron emission tomography using 11 C-N-methyl-spiperone. Acta Neurol Scand 1987; 75: 87-94
-
(1987)
Acta Neurol Scand
, vol.75
, pp. 87-94
-
-
Hagglund, J.1
Aqullonius, S.M.2
Eckernas, S.A.3
-
212
-
-
0037408213
-
Progressive striatal and cortical dopamine receptor dysfunction in Huntington's disease: A pet study
-
DOI 10.1093/brain/awg119
-
Pavese N, Andrews TC, Brooks DJ et al. Progressive striatal and cortical dopamine receptor dysfunction in Huntington's disease: a PET study. Brain 2003; 126: 1127-1135 (Pubitemid 36522955)
-
(2003)
Brain
, vol.126
, Issue.5
, pp. 1127-1135
-
-
Pavese, N.1
Andrews, T.C.2
Brooks, D.J.3
Ho, A.K.4
Rosser, A.E.5
Barker, R.A.6
Robbins, T.W.7
Sahakian, B.J.8
Dunnett, S.B.9
Piccini, P.10
-
213
-
-
12644252940
-
Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington's disease
-
Antonini A, Leenders KL, Spiegel R et al. Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington's disease. Brain 1996; 119: 2085-2095
-
(1996)
Brain
, vol.119
, pp. 2085-2095
-
-
Antonini, A.1
Leenders, K.L.2
Spiegel, R.3
-
214
-
-
25444467559
-
Striatal dopamine D2 receptors, metabolism, and volume in preclinical Huntington disease
-
van Oostrom JC, Magulre RP, Verschuuren-Bemelmans CC et al. Striatal dopamine D2 receptors, metabolism, and volume in preclinical Huntington disease. Neurology 2005; 65: 941-943
-
(2005)
Neurology
, vol.65
, pp. 941-943
-
-
Van Oostrom, J.C.1
Magulre, R.P.2
Verschuuren-Bemelmans, C.C.3
-
215
-
-
0030763985
-
Central motor processing in Huntington's disease
-
Bartenstein P, Weindl A, Spiegel S et al. Central motor processing in Huntington's disease. A PET study. Brain 1997; 120: 1553-1567
-
(1997)
A PET Study. Brain
, vol.120
, pp. 1553-1567
-
-
Bartenstein, P.1
Weindl, A.2
Spiegel, S.3
-
216
-
-
0032834956
-
Sensory processing in Parkinson's and Huntington's disease: Investigations with 3D H(2)(15)0-PET
-
Boecker H, Ceballos-Baumann A, Bartenstein P et al. Sensory processing in Parkinson's and Huntington's disease: investigations with 3D H(2)(15)0-PET. Brain 1999; 122: 1651-1665
-
(1999)
Brain
, vol.122
, pp. 1651-1665
-
-
Boecker, H.1
Ceballos-Baumann, A.2
Bartenstein, P.3
-
217
-
-
33745637954
-
Microglial activation correlates with severity in Huntington disease: A clinical and PET study
-
DOI 10.1212/01.wnl.0000222734.56412.17, PII 0000611420060613000008
-
Pavese N, Gerhard A, Tai YF et al. Microglial activation correlates with severity in Huntington disease: a clinical and PET study. Neurology 2006; 66: 1638-1643 (Pubitemid 43964614)
-
(2006)
Neurology
, vol.66
, Issue.11
, pp. 1638-1643
-
-
Pavese, N.1
Gerhard, A.2
Tai, Y.F.3
Ho, A.K.4
Turkheimer, F.5
Barker, R.A.6
Brooks, D.J.7
Piccini, P.8
-
218
-
-
34447636065
-
Microglial activation in presymptomatic Huntington's disease gene carriers
-
DOI 10.1093/brain/awm044
-
Tai YF, Pavese N, Gerhard A et al. Microglial activation in presymptomatic Huntington's disease gene carriers. Brain 2007; 130: 1759-1766 (Pubitemid 47343790)
-
(2007)
Brain
, vol.130
, Issue.7
, pp. 1759-1766
-
-
Tai, Y.F.1
Pavese, N.2
Gerhard, A.3
Tabrizi, S.J.4
Barker, R.A.5
Brooks, D.J.6
Piccini, P.7
-
219
-
-
35648963039
-
Thalamic metabolism and symptom onset in preclinical Huntington's disease
-
DOI 10.1093/brain/awm217
-
Feigin A, Tang C, Ma Y et al. Thalamic metabolism and symptom onset in preclinical Huntington's disease. Brain 2007; 130: 2858-2867 (Pubitemid 350033965)
-
(2007)
Brain
, vol.130
, Issue.11
, pp. 2858-2867
-
-
Feigin, A.1
Tang, C.2
Ma, Y.3
Mattis, P.4
Zgaljardic, D.5
Guttman, M.6
Paulsen, J.S.7
Dhawan, V.8
Eidelberg, D.9
-
220
-
-
23344448837
-
Genome-wide expression profiling of human blood reveals biomarkers for Huntington's disease
-
Boroveckl F, Lovreclc L Zhou J et al. Genome-wide expression profiling of human blood reveals biomarkers for Huntington's disease. PNAS (USA) 2005; 102: 11023-11028
-
(2005)
PNAS (USA)
, vol.102
, pp. 11023-11028
-
-
Boroveckl, F.1
Lovreclc, L.2
Zhou, J.3
-
221
-
-
35448968328
-
Analysis of potential transcriptomic biomarkers for Huntington's disease in peripheral blood
-
DOI 10.1073/pnas.0703652104
-
Runne H, Kuhn A, Wild EJ et al. Analysis of potential transcriptomic biomarkers for Huntington's disease in peripheral blood. PNAS (USA) 2007; 104: 14424-14429 (Pubitemid 350003277)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.36
, pp. 14424-14429
-
-
Runne, H.1
Kuhn, A.2
Wild, E.J.3
Pratyaksha, W.4
Kristiansen, M.5
Isaacs, J.D.6
Regulier, E.7
Delorenzi, M.8
Tabrizi, S.J.9
Luthi-Carter, R.10
-
222
-
-
56549119132
-
Optimisation of region-specific reference gene selection and relative gene expression analysis methods for pre-clinical trials of Huntington's disease
-
Benn CL, Fox H, Bates GP. Optimisation of region-specific reference gene selection and relative gene expression analysis methods for pre-clinical trials of Huntington's disease. Mol Neurodegener 2008; 3: 17
-
(2008)
Mol Neurodegener
, vol.3
, pp. 17
-
-
Benn, C.L.1
Fox, H.2
Bates, G.P.3
-
223
-
-
25844526181
-
Gene expression in Huntington's disease skeletal muscle: A potential biomarker
-
DOI 10.1093/hmg/ddi192
-
Strand AD, Aragakl AK, Shaw D et al. Gene expression in Huntington's disease skeletal muscle: a potential biomarker. Hum Mol Gen 2005; 14: 1863-1876 (Pubitemid 41418057)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.13
, pp. 1863-1876
-
-
Strand, A.D.1
Aragaki, A.K.2
Shaw, D.3
Bird, T.4
Holton, J.5
Turner, C.6
Tapscott, S.J.7
Tabrizi, S.J.8
Schapira, A.H.9
Kooperberg, C.10
Olson, J.M.11
-
224
-
-
0036582045
-
Alterations in the mouse and human proteome caused by Huntington's disease
-
Zabel C, Chamrad DC, Priller J et al. Alterations in the mouse and human proteome caused by Huntington's disease. Mol Cell Proteomics 2002; 1: 366-375
-
(2002)
Mol Cell Proteomics
, vol.1
, pp. 366-375
-
-
Zabel, C.1
Chamrad, D.C.2
Priller, J.3
-
226
-
-
33746883938
-
Cerebrospinal fluid levels of orexin - A are not a clinically useful biomarker for Huntington disease
-
Bjorkqvlst M, Petersen A, Nielsen J et al. Cerebrospinal fluid levels of orexin - A are not a clinically useful biomarker for Huntington disease. Clin Genet 2006; 70: 78-79
-
(2006)
Clin Genet
, vol.70
, pp. 78-79
-
-
Bjorkqvlst, M.1
Petersen, A.2
Nielsen, J.3
-
227
-
-
56149125562
-
Weight loss in Huntington disease increases with higher CAG repeat number
-
Aziz NA, van der Burg JM, Landwehrmeyer GB et al. Weight loss in Huntington disease increases with higher CAG repeat number. Neurology 2008; 71: 1506-1513
-
(2008)
Neurology
, vol.71
, pp. 1506-1513
-
-
Aziz, N.A.1
Van Der Burg, J.M.2
Landwehrmeyer, G.B.3
-
228
-
-
34548379904
-
Cholesterol biosynthesis pathway is disturbed in YAC128 mice and is modulated by huntingtin mutation
-
DOI 10.1093/hmg/ddm170
-
Valenza M, CarrollJB, Leonl V et al. Cholesterol biosynthesis pathway is disturbed in YAC128 mice and is modulated by huntingtin mutation. Hum Mol Gen 2007; 16: 2187-2198 (Pubitemid 47354901)
-
(2007)
Human Molecular Genetics
, vol.16
, Issue.18
, pp. 2187-2198
-
-
Valenza, M.1
Carroll, J.B.2
Leoni, V.3
Bertram, L.N.4
Bjorkhem, I.5
Singaraja, R.R.6
Lutjohann, D.7
Hayden, M.R.8
Cattaneo, E.9
-
229
-
-
34548777515
-
Progressive dysfunction of the cholesterol biosynthesis pathway in the R6/2 mouse model of Huntington's disease
-
DOI 10.1016/j.nbd.2007.07.004, PII S096999610700143X
-
Valenza M, Leoni V, Tarditi A et al. Progressive dysfunction of the cholesterol biosynthesis pathway in the R6/2 mouse model of Huntington's disease. Neurobiol Dis 2007; 28: 133-142 (Pubitemid 47429978)
-
(2007)
Neurobiology of Disease
, vol.28
, Issue.1
, pp. 133-142
-
-
Valenza, M.1
Leoni, V.2
Tarditi, A.3
Mariotti, C.4
Bjorkhem, I.5
Cattaneo, E.6
-
230
-
-
55749085638
-
Plasma 24S-hydroxycholesterol and caudate MRI in pre-manifest and early Huntington's disease
-
Leoni V, Mariotti C, Tabrizi SJ et al. Plasma 24S-hydroxycholesterol and caudate MRI in pre-manifest and early Huntington's disease. Brain 2008; 131: 2851-2859
-
(2008)
Brain
, vol.131
, pp. 2851-2859
-
-
Leoni, V.1
Mariotti, C.2
Tabrizi, S.J.3
-
231
-
-
33644843611
-
1H NMR spectroscopy
-
DOI 10.1021/pr050244o
-
Tsang TM, Woodman B, McLoughlin GA et al. Metabolic characterization of the R6/2 transgenic mouse model of Huntington's disease by high-resolution MAS IH NMR spectroscopy. J Proteome Res 2006; 5: 483-492 (Pubitemid 43364087)
-
(2006)
Journal of Proteome Research
, vol.5
, Issue.3
, pp. 483-492
-
-
Tsang, T.M.1
Woodman, B.2
Mcloughlin, G.A.3
Griffin, J.L.4
Tabrizi, S.J.5
Bates, G.P.6
Holmes, E.7
-
232
-
-
33745210300
-
Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease
-
DOI 10.1093/hmg/ddl094
-
Bjorkqvist M, Petersen A, Bacos K et al. Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease. Hum Mol Gen 2006; 15: 1713-1721 (Pubitemid 43904837)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.10
, pp. 1713-1721
-
-
Bjorkqvist, M.1
Petersen, A.2
Bacos, K.3
Isaacs, J.4
Norlen, P.5
Gil, J.6
Popovic, N.7
Sundler, F.8
Bates, G.P.9
Tabrizi, S.J.10
Brundin, P.11
Mulder, H.12
-
233
-
-
65249112842
-
Increased hypothalamic-pituitary-adrenal axis activity in Huntington's disease
-
Aziz NA, Pijl H, Frolich M et al. Increased hypothalamic-pituitary- adrenal axis activity in Huntington's disease. J Clin Endocrinol Metab 2009; 94: 1223-1228
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 1223-1228
-
-
Aziz, N.A.1
Pijl, H.2
Frolich, M.3
-
234
-
-
63449102847
-
Neuroendocrine disturbances in Huntington's disease
-
Saleh N, Moutereau S, Durr A et al. Neuroendocrine disturbances in Huntington's disease. PLoS ONE 2009; 4: e4962
-
(2009)
PLoS ONE
, vol.4
-
-
Saleh, N.1
Moutereau, S.2
Durr, A.3
-
235
-
-
55749087155
-
Hypothalamic involvement in Huntington's disease: An in vivo PET study
-
Politis M, Pavese N, Tai YF et al. Hypothalamic involvement in Huntington's disease: an in vivo PET study. Brain 2008; 131: 2860-2869
-
(2008)
Brain
, vol.131
, pp. 2860-2869
-
-
Politis, M.1
Pavese, N.2
Tai, Y.F.3
-
236
-
-
33750437278
-
Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1α in Huntington's disease neurodegeneration
-
DOI 10.1016/j.cmet.2006.10.004, PII S1550413106003329
-
Weydt P, Pineda W, Torrence AE et al. Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1alpha in Huntington's disease neurodegeneration. Cell Metab 2006; 4: 349-362 (Pubitemid 44645069)
-
(2006)
Cell Metabolism
, vol.4
, Issue.5
, pp. 349-362
-
-
Weydt, P.1
Pineda, V.V.2
Torrence, A.E.3
Libby, R.T.4
Satterfield, T.F.5
Lazarowski, E.6
Gilbert, M.L.7
Morton, G.J.8
Bammler, T.K.9
Strand, A.D.10
Cui, L.11
Beyer, R.P.12
Easley, C.N.13
Smith, A.C.14
Krainc, D.15
Luquet, S.16
Sweet, I.17
Schwartz, M.W.18
La, S.19
-
237
-
-
36249001659
-
Cocaine- And amphetamineregulated transcript is increased in Huntington disease
-
Bjorkqvist M, Leavitt BR, Nielsen JE et al. Cocaine- and amphetamineregulated transcript is increased in Huntington disease. Mov Disord 2007; 22: 1952-1954
-
(2007)
Mov Disord
, vol.22
, pp. 1952-1954
-
-
Bjorkqvist, M.1
Leavitt, B.R.2
Nielsen, J.E.3
-
238
-
-
33749014170
-
Selective reduction of amyloid β42 discriminates Alzheimer's disease from Huntington's disease: Indication for distinct pathological events in amyloid β peptide aggregation [7]
-
DOI 10.1136/jnnp.2005.084673
-
Mollenhauer B, Bibl M, Esselmann H et al. Selective reduction of amyloid beta42 discriminates Alzheimer's disease from Huntington's disease: indication for distinct pathological events in amyloid beta peptide aggregation. J Neurol Neurosurg Psychiatry 2006; 77: 1201-1203 (Pubitemid 44453264)
-
(2006)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.77
, Issue.10
, pp. 1201-1203
-
-
Mollenhauer, B.1
Bibl, M.2
Esselmann, H.3
Steinacker, P.4
Trenkwalder, C.5
Brechlin, P.6
Wiltfang, J.7
Otto, M.8
-
239
-
-
43549109224
-
Applications in brain proteomies: 8(th) HUPO Brain Proteome Project Workshop 7 October 2007Seoul, Korea
-
Hamacher M, Stephan C, Hardt T et al. Applications in brain proteomies: 8(th) HUPO Brain Proteome Project Workshop 7 October 2007, Seoul, Korea. Proteomics 2008; 8: 1750-1753
-
(2008)
Proteomics
, vol.8
, pp. 1750-1753
-
-
Hamacher, M.1
Stephan, C.2
Hardt, T.3
-
240
-
-
63049118268
-
Brain-specific proteins decline in the cerebrospinal fluid of humans with Huntington disease
-
Fang Q, Strand A, Law Wet al. Brain-specific proteins decline in the cerebrospinal fluid of humans with Huntington disease. MoI Cell Proteomics 2009; 8: 451-466
-
(2009)
MoI Cell Proteomics
, vol.8
, pp. 451-466
-
-
Fang, Q.1
Strand, A.2
Law, W.3
-
241
-
-
34547167008
-
Proteomic profiling of plasma in Huntington's disease reveals neuroinflammatory activation and biomarker candidates
-
DOI 10.1021/pr0700753
-
DalrympleA, Wild EJ, Joubert R et al. Proteomic profiling of plasma in Huntington's disease reveals neuroinflammatory activation and biomarker candidates. J Proteome Res 2007; 6: 2833-2840 (Pubitemid 47122377)
-
(2007)
Journal of Proteome Research
, vol.6
, Issue.7
, pp. 2833-2840
-
-
Dalrymple, A.1
Wild, E.J.2
Joubert, R.3
Sathasivam, K.4
Bjorkqvist, M.5
Petersen, A.6
Jackson, G.S.7
Isaacs, J.D.8
Kristiansen, M.9
Bates, G.P.10
Leavitt, B.R.11
Keir, G.12
Ward, M.13
Tabrizi, S.J.14
-
242
-
-
0031743376
-
Activated immune system in patients with Huntington's disease
-
LebihuberF, Walli J, Jellinger K et al. Activated immune system in patients with Huntington's disease. Clin Chem Lab Med 1998; 36: 747-750 (Pubitemid 28521525)
-
(1998)
Clinical Chemistry and Laboratory Medicine
, vol.36
, Issue.10
, pp. 747-750
-
-
Leblhuber, F.1
Walli, J.2
Jellinger, K.3
Tilz, G.P.4
Widner, B.5
Laccone, F.6
Fuchs, D.7
-
243
-
-
0032873347
-
Increased complement biosynthesis by microglia and complement activation on neurons in Huntington's disease
-
Singhrao SK, Neal JW, Morgan BP et al. Increased complement biosynthesis by microglia and complement activation on neurons in Huntington's disease. Exp Neurol 1999; 159: 362-376
-
(1999)
Exp Neurol
, vol.159
, pp. 362-376
-
-
Singhrao, S.K.1
Neal, J.W.2
Morgan, B.P.3
-
244
-
-
49249089029
-
A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease
-
Bjorkqvlst M, Wild EJ, Thiele J et al. A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease.J Exp Med 2008; 205: 1869-1877
-
(2008)
J Exp Med
, vol.205
, pp. 1869-1877
-
-
Bjorkqvlst, M.1
Wild, E.J.2
Thiele, J.3
-
246
-
-
43449115426
-
Maintaining standardization: An update of the HUPO Brain Proteome Project
-
DOI 10.1586/14789450.5.2.165
-
Hamacher M, Stephan C, Elsenacher M et al. Maintaining standardization: an update of the HUPO Brain Proteome Project. Expert Rev Proteomics 2008; 5: 165-173 (Pubitemid 351670923)
-
(2008)
Expert Review of Proteomics
, vol.5
, Issue.2
, pp. 165-173
-
-
Hamacher, M.1
Stephan, C.2
Eisenacher, M.3
Hardt, T.4
Marcus, K.5
Meyer, H.E.6
-
247
-
-
43349093004
-
Installation and use of the Computational Proteomics Analysis System (CPAS)
-
Chapter 13: Unit
-
Myers T, Law W, Eng JK et al. Installation and use of the Computational Proteomics Analysis System (CPAS). Current protocols in bioinformatics 2007; Chapter 13: Unit 13-15
-
(2007)
Current Protocols in Bioinformatics
, pp. 13-15
-
-
Myers, T.1
Law, W.2
Eng, J.K.3
-
248
-
-
0037101835
-
Dysregulation of gene expression in the R6/2 model of polyglutamine disease: Parallel changes in muscle and brain
-
Luthi-Carter R, Hanson SA, Strand AD et al. Dysregulation of gene expression in the R6/2 model of polyglutamine disease: parallel changes in muscle and brain. Hum Mol Gen 2002; 11: 1911-1926 (Pubitemid 34928255)
-
(2002)
Human Molecular Genetics
, vol.11
, Issue.17
, pp. 1911-1926
-
-
Luthi-Carter, R.1
Hanson, S.A.2
Strand, A.D.3
Bergstrom, D.A.4
Chun, W.5
Peters, N.L.6
Woods, A.M.7
Chan, E.Y.8
Kooperberg, C.9
Krainc, D.10
Young, A.B.11
Tapscott, S.J.12
Olson, J.M.13
-
249
-
-
33745134073
-
2A receptor signaling in a mouse model of Huntington disease
-
DOI 10.1016/j.nbd.2006.01.014, PII S0969996106000180
-
Tarditi A, Camurri A, Varani K et al. Early and transient alteration of adenosine A2A receptor signaling in a mouse model of Huntington disease. Neurobiol Dis 2006; 23: 44-53 (Pubitemid 43903630)
-
(2006)
Neurobiology of Disease
, vol.23
, Issue.1
, pp. 44-53
-
-
Tarditi, A.1
Camurri, A.2
Varani, K.3
Borea, P.A.4
Woodman, B.5
Bates, G.6
Cattaneo, E.7
Abbracchio, M.P.8
-
250
-
-
0024802071
-
Ethical issues policy statement on Huntington's disease molecular genetics predictive test
-
World Federation of Neurology: Research Committee. Research Group on Huntington's chorea..
-
World Federation of Neurology: Research Committee. Research Group on Huntington's chorea.. Ethical issues policy statement on Huntington's disease molecular genetics predictive test. J Neurol Sci 1989; 94: 327-332
-
(1989)
J Neurol Sci
, vol.94
, pp. 327-332
-
-
-
251
-
-
0025059035
-
Ethical issues policy statement on Huntington's disease molecular genetics predictive test
-
International Huntington Association. World Federation of Neurology.
-
Went L Ethical issues policy statement on Huntington's disease molecular genetics predictive test. International Huntington Association. World Federation of Neurology. J Med Genet 1990; 27: 34-38
-
(1990)
J Med Genet
, vol.27
, pp. 34-38
-
-
Went, L.1
|