-
1
-
-
0038441892
-
Task-set switching deficits in early-stage Huntington's disease: implications for basal ganglia function
-
Aron A.R., Watkins L., Sahakian B.J., Monsell S., Barker R.A., Robbins T.W. Task-set switching deficits in early-stage Huntington's disease: implications for basal ganglia function. J. Cogn. Neurosci. 2003, 15:629-642.
-
(2003)
J. Cogn. Neurosci.
, vol.15
, pp. 629-642
-
-
Aron, A.R.1
Watkins, L.2
Sahakian, B.J.3
Monsell, S.4
Barker, R.A.5
Robbins, T.W.6
-
2
-
-
0031950826
-
Frontal lobe volume in patients with Huntington's disease
-
Aylward E.H., Anderson N.B., Bylsma F.W., Wagster M.V., Barta P.E., Sherr M., Feeney J., Davis A., Rosenblatt A., Pearlson G.D., Ross C.A. Frontal lobe volume in patients with Huntington's disease. Neurology 1998, 50:252-258.
-
(1998)
Neurology
, vol.50
, 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
-
3
-
-
0035942320
-
Retest effects and cognitive decline in longitudinal follow-up of patients with early HD
-
Bachoud-Levi A.C., Maison P., Bartolomeo P., Boisse M.F., Dalla B.G., Ergis A.M., Baudic S., Degos J.D., Cesaro P., Peschanski M. Retest effects and cognitive decline in longitudinal follow-up of patients with early HD. Neurology 2001, 56:1052-1058.
-
(2001)
Neurology
, vol.56
, pp. 1052-1058
-
-
Bachoud-Levi, A.C.1
Maison, P.2
Bartolomeo, P.3
Boisse, M.F.4
Dalla, B.G.5
Ergis, A.M.6
Baudic, S.7
Degos, J.D.8
Cesaro, P.9
Peschanski, M.10
-
4
-
-
67349224632
-
Subtle but progressive cognitive deficits in the female tgHD hemizygote rat as demonstrated by operant SILT performance
-
Brooks S., Fielding S., Dobrossy M., von Horsten S., Dunnett S. Subtle but progressive cognitive deficits in the female tgHD hemizygote rat as demonstrated by operant SILT performance. Brain Res. Bull. 2009, 79:310-315.
-
(2009)
Brain Res. Bull.
, vol.79
, pp. 310-315
-
-
Brooks, S.1
Fielding, S.2
Dobrossy, M.3
von Horsten, S.4
Dunnett, S.5
-
5
-
-
80054735497
-
Longitudinal analysis of the behavioural phenotype in YAC128 (C57BL/6J) Huntington's disease transgenic mice
-
Brooks S., Higgs G., Janghra N., Jones L., Dunnett S.B. Longitudinal analysis of the behavioural phenotype in YAC128 (C57BL/6J) Huntington's disease transgenic mice. Brain Res. Bull. 2010.
-
(2010)
Brain Res. Bull.
-
-
Brooks, S.1
Higgs, G.2
Janghra, N.3
Jones, L.4
Dunnett, S.B.5
-
6
-
-
36448950196
-
Striatal lesions in the mouse disrupt acquisition and retention, but not implicit learning, in the SILT procedural motor learning task
-
Brooks S.P., Trueman R.C., Dunnett S.B. Striatal lesions in the mouse disrupt acquisition and retention, but not implicit learning, in the SILT procedural motor learning task. Brain Res. 2007, 1185:179-188.
-
(2007)
Brain Res.
, vol.1185
, pp. 179-188
-
-
Brooks, S.P.1
Trueman, R.C.2
Dunnett, S.B.3
-
7
-
-
0035164479
-
Dissociation between intentional and incidental sequence learning in Huntington's disease
-
Brown R.G., Redondo-Verge L., Chacon J.R., Lucas M.L., Channon S. Dissociation between intentional and incidental sequence learning in Huntington's disease. Brain 2001, 124:2188-2202.
-
(2001)
Brain
, vol.124
, pp. 2188-2202
-
-
Brown, R.G.1
Redondo-Verge, L.2
Chacon, J.R.3
Lucas, M.L.4
Channon, S.5
-
8
-
-
43049165309
-
Orienting of spatial attention in Huntington's disease
-
Couette M., Bachoud-Levi A.C., Brugieres P., Sieroff E., Bartolomeo P. Orienting of spatial attention in Huntington's disease. Neuropsychologia 2008, 46:1391-1400.
-
(2008)
Neuropsychologia
, vol.46
, pp. 1391-1400
-
-
Couette, M.1
Bachoud-Levi, A.C.2
Brugieres, P.3
Sieroff, E.4
Bartolomeo, P.5
-
9
-
-
18544410106
-
Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
-
Davies S.W., Turmaine M., Cozens B.A., DiFiglia M., Sharp A.H., Ross C.A., Scherzinger E., Wanker E.E., Mangiarini L., Bates G.P. Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation. Cell 1997, 90:537-548.
-
(1997)
Cell
, vol.90
, pp. 537-548
-
-
Davies, S.W.1
Turmaine, M.2
Cozens, B.A.3
DiFiglia, M.4
Sharp, A.H.5
Ross, C.A.6
Scherzinger, E.7
Wanker, E.E.8
Mangiarini, L.9
Bates, G.P.10
-
10
-
-
49649104080
-
Implicit and explicit aspects of sequence learning in pre-symptomatic Huntington's disease
-
Ghilardi M.F., Silvestri G., Feigin A., Mattis P., Zgaljardic D., Moisello C., Crupi D., Marinelli L., Dirocco A., Eidelberg D. Implicit and explicit aspects of sequence learning in pre-symptomatic Huntington's disease. Parkinsonism Relat. Disord. 2008, 14:457-464.
-
(2008)
Parkinsonism Relat. Disord.
, vol.14
, pp. 457-464
-
-
Ghilardi, M.F.1
Silvestri, G.2
Feigin, A.3
Mattis, P.4
Zgaljardic, D.5
Moisello, C.6
Crupi, D.7
Marinelli, L.8
Dirocco, A.9
Eidelberg, D.10
-
11
-
-
0022100186
-
Implicit and explicit memory for new associations in normal and amnesic subjects
-
Graf P., Schacter D.L. Implicit and explicit memory for new associations in normal and amnesic subjects. J. Exp. Psychol. Learn. Memory Cogn. 1985, 11:501-518.
-
(1985)
J. Exp. Psychol. Learn. Memory Cogn.
, vol.11
, pp. 501-518
-
-
Graf, P.1
Schacter, D.L.2
-
12
-
-
46749157501
-
Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD mice
-
Gray M., Shirasaki D.I., Cepeda C., Andre V.M., Wilburn B., Lu X.H., Tao J., Yamazaki I., Li S.H., Sun Y.E., Li X.J., Levine M.S., Yang X.W. Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD mice. J. Neurosci. 2008, 28:6182-6195.
-
(2008)
J. Neurosci.
, vol.28
, pp. 6182-6195
-
-
Gray, M.1
Shirasaki, D.I.2
Cepeda, C.3
Andre, V.M.4
Wilburn, B.5
Lu, X.H.6
Tao, J.7
Yamazaki, I.8
Li, S.H.9
Sun, Y.E.10
Li, X.J.11
Levine, M.S.12
Yang, X.W.13
-
13
-
-
0024503945
-
Neuropsychological evidence for multiple implicit memory systems: a comparison of Alzheimer's, Huntington's, and Parkinson's disease patients
-
Heindel W.C., Salmon D.P., Shults C.W., Walicke P.A., Butters N. Neuropsychological evidence for multiple implicit memory systems: a comparison of Alzheimer's, Huntington's, and Parkinson's disease patients. J. Neurosci. 1989, 9:582-587.
-
(1989)
J. Neurosci.
, vol.9
, pp. 582-587
-
-
Heindel, W.C.1
Salmon, D.P.2
Shults, C.W.3
Walicke, P.A.4
Butters, N.5
-
14
-
-
9144259577
-
Profile of cognitive progression in early Huntington's disease
-
Ho A.K., Sahakian B.J., Brown R.G., Barker R.A., Hodges J.R., Ane M.N., Snowden J., Thompson J., Esmonde T., Gentry R., Moore J.W., Bodner T. Profile of cognitive progression in early Huntington's disease. Neurology 2003, 61:1702-1706.
-
(2003)
Neurology
, vol.61
, 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
-
15
-
-
34249891319
-
An operant serial implicit learning task (SILT) in rats: task acquisition, performance and the effects of striatal lesions
-
Jay J.R., Dunnett S.B. An operant serial implicit learning task (SILT) in rats: task acquisition, performance and the effects of striatal lesions. J. Neurosci. Methods 2007, 163:235-244.
-
(2007)
J. Neurosci. Methods
, vol.163
, pp. 235-244
-
-
Jay, J.R.1
Dunnett, S.B.2
-
16
-
-
0021061919
-
Development of neuropsychological deficits in Huntington's disease
-
Josiassen R.C., Curry L.M., Mancall E.L. Development of neuropsychological deficits in Huntington's disease. Arch. Neurol. 1983, 40:791-796.
-
(1983)
Arch. Neurol.
, vol.40
, pp. 791-796
-
-
Josiassen, R.C.1
Curry, L.M.2
Mancall, E.L.3
-
17
-
-
3042832791
-
Functional MRI study of a serial reaction time task in Huntington's disease
-
Kim J.S., Reading S.A., Brashers-Krug T., Calhoun V.D., Ross C.A., Pearlson G.D. 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
Calhoun, V.D.4
Ross, C.A.5
Pearlson, G.D.6
-
18
-
-
0025727341
-
Procedural learning is impaired in Huntington's disease: evidence from the serial reaction time task
-
Knopman D., Nissen M.J. Procedural learning is impaired in Huntington's disease: evidence from the serial reaction time task. Neuropsychologia 1991, 29:245-254.
-
(1991)
Neuropsychologia
, vol.29
, pp. 245-254
-
-
Knopman, D.1
Nissen, M.J.2
-
19
-
-
0031814175
-
Evidence for specific cognitive deficits in preclinical Huntington's disease
-
Lawrence A.D., Hodges J.R., Rosser A.E., Kershaw A., Ffrench-Constant C., Rubinsztein D.C., Robbins T.W., Sahakian B.J. Evidence for specific cognitive deficits in preclinical Huntington's disease. Brain 1998, 121(Pt 7):1329-1341.
-
(1998)
Brain
, vol.121
, Issue.PART 7
, pp. 1329-1341
-
-
Lawrence, A.D.1
Hodges, J.R.2
Rosser, A.E.3
Kershaw, A.4
Ffrench-Constant, C.5
Rubinsztein, D.C.6
Robbins, T.W.7
Sahakian, B.J.8
-
20
-
-
0035862896
-
Neurological abnormalities in a knock-in mouse model of Huntington's disease
-
Lin C.H., Tallaksen-Greene S., Chien W.M., Cearley J.A., Jackson W.S., Crouse A.B., Ren S., Li X.J., Albin R.L., Detloff P.J. Neurological abnormalities in a knock-in mouse model of Huntington's disease. Hum. Mol. Genet. 2001, 10:137-144.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 137-144
-
-
Lin, C.H.1
Tallaksen-Greene, S.2
Chien, W.M.3
Cearley, J.A.4
Jackson, W.S.5
Crouse, A.B.6
Ren, S.7
Li, X.J.8
Albin, R.L.9
Detloff, P.J.10
-
21
-
-
16044373842
-
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
-
Mangiarini L., Sathasivam K., Seller M., Cozens B., Harper A., Hetherington C., Lawton M., Trottier Y., Lehrach H., Davies S.W., Bates G.P. Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. Cell 1996, 87:493-506.
-
(1996)
Cell
, vol.87
, pp. 493-506
-
-
Mangiarini, L.1
Sathasivam, K.2
Seller, M.3
Cozens, B.4
Harper, A.5
Hetherington, C.6
Lawton, M.7
Trottier, Y.8
Lehrach, H.9
Davies, S.W.10
Bates, G.P.11
-
22
-
-
68249155312
-
Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models
-
Menalled L., El Khodor B.F., Patry M., Suarez-Farinas M., Orenstein S.J., Zahasky B., Leahy C., Wheeler V., Yang X.W., MacDonald M., Morton A.J., Bates G., Leeds J., Park L., Howland D., Signer E., Tobin A., Brunner D. Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models. Neurobiol. Dis. 2009, 35:319-336.
-
(2009)
Neurobiol. Dis.
, vol.35
, pp. 319-336
-
-
Menalled, L.1
El Khodor, B.F.2
Patry, M.3
Suarez-Farinas, M.4
Orenstein, S.J.5
Zahasky, B.6
Leahy, C.7
Wheeler, V.8
Yang, X.W.9
MacDonald, M.10
Morton, A.J.11
Bates, G.12
Leeds, J.13
Park, L.14
Howland, D.15
Signer, E.16
Tobin, A.17
Brunner, D.18
-
23
-
-
0037107191
-
Early motor dysfunction and striosomal distribution of huntingtin microaggregates in Huntington's disease knock-in mice
-
Menalled L.B., Sison J.D., Wu Y., Olivieri M., Li X.J., Li H., Zeitlin S., Chesselet M.F. Early motor dysfunction and striosomal distribution of huntingtin microaggregates in Huntington's disease knock-in mice. J. Neurosci. 2002, 22:8266-8276.
-
(2002)
J. Neurosci.
, vol.22
, pp. 8266-8276
-
-
Menalled, L.B.1
Sison, J.D.2
Wu, Y.3
Olivieri, M.4
Li, X.J.5
Li, H.6
Zeitlin, S.7
Chesselet, M.F.8
-
24
-
-
77955359169
-
Quantitative relationships between huntingtin levels, polyglutamine length, inclusion body formation, and neuronal death provide novel insight into Huntington's disease molecular pathogenesis
-
Miller J., Arrasate M., Shaby B.A., Mitra S., Masliah E., Finkbeiner S. Quantitative relationships between huntingtin levels, polyglutamine length, inclusion body formation, and neuronal death provide novel insight into Huntington's disease molecular pathogenesis. J. Neurosci. 2010, 30:10541-10550.
-
(2010)
J. Neurosci.
, vol.30
, pp. 10541-10550
-
-
Miller, J.1
Arrasate, M.2
Shaby, B.A.3
Mitra, S.4
Masliah, E.5
Finkbeiner, S.6
-
25
-
-
0034958203
-
Progressive formation of inclusions in the striatum and hippocampus of mice transgenic for the human Huntington's disease mutation
-
Morton A.J., Lagan M.A., Skepper J.N., Dunnett S.B. Progressive formation of inclusions in the striatum and hippocampus of mice transgenic for the human Huntington's disease mutation. J. Neurocytol. 2000, 29:679-702.
-
(2000)
J. Neurocytol.
, vol.29
, pp. 679-702
-
-
Morton, A.J.1
Lagan, M.A.2
Skepper, J.N.3
Dunnett, S.B.4
-
26
-
-
65249132310
-
Prevention of depressive behaviour in the YAC128 mouse model of Huntington disease by mutation at residue 586 of huntingtin
-
Pouladi M.A., Graham R.K., Karasinska J.M., Xie Y., Santos R.D., Petersen A., Hayden M.R. Prevention of depressive behaviour in the YAC128 mouse model of Huntington disease by mutation at residue 586 of huntingtin. Brain 2009, 132:919-932.
-
(2009)
Brain
, vol.132
, pp. 919-932
-
-
Pouladi, M.A.1
Graham, R.K.2
Karasinska, J.M.3
Xie, Y.4
Santos, R.D.5
Petersen, A.6
Hayden, M.R.7
-
27
-
-
0032468401
-
Is there a subcortical profile of attentional dysfunction? A comparison of patients with Huntington's and Parkinson's diseases on a global-local focused attention task
-
Roman M.J., Delis D.C., Filoteo J.V., Demadura T.L., Paulsen J., Swerdlow N.R., Swenson M.R., Salmon D., Butters N., Shults C. Is there a subcortical profile of attentional dysfunction? A comparison of patients with Huntington's and Parkinson's diseases on a global-local focused attention task. J. Clin. Exp. Neuropsychol. 1998, 20:873-884.
-
(1998)
J. Clin. Exp. Neuropsychol.
, vol.20
, pp. 873-884
-
-
Roman, M.J.1
Delis, D.C.2
Filoteo, J.V.3
Demadura, T.L.4
Paulsen, J.5
Swerdlow, N.R.6
Swenson, M.R.7
Salmon, D.8
Butters, N.9
Shults, C.10
-
28
-
-
24644479046
-
Regional cortical thinning in preclinical Huntington disease and its relationship to cognition
-
Rosas H.D., Hevelone N.D., Zaleta A.K., Greve D.N., Salat D.H., Fischl B. 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
Greve, D.N.4
Salat, D.H.5
Fischl, B.6
-
29
-
-
0037066115
-
Regional and progressive thinning of the cortical ribbon in Huntington's disease
-
Rosas H.D., Liu A.K., Hersch S., Glessner M., Ferrante R.J., Salat D.H., van der K.A., Jenkins B.G., Dale A.M., Fischl B. Regional and progressive thinning of the cortical ribbon in Huntington's disease. Neurology 2002, 58:695-701.
-
(2002)
Neurology
, vol.58
, 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 der, K.A.7
Jenkins, B.G.8
Dale, A.M.9
Fischl, B.10
-
30
-
-
41849133159
-
Cerebral cortex and the clinical expression of Huntington's disease: complexity and heterogeneity
-
Rosas H.D., Salat D.H., Lee S.Y., Zaleta A.K., Pappu V., Fischl B., Greve D., Hevelone N., Hersch S.M. 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
Zaleta, A.K.4
Pappu, V.5
Fischl, B.6
Greve, D.7
Hevelone, N.8
Hersch, S.M.9
-
31
-
-
0023780253
-
Procedural learning and neostriatal dysfunction in man
-
Saint-Cyr J.A., Taylor A.E., Lang A.E. Procedural learning and neostriatal dysfunction in man. Brain 1988, 111(Pt 4):941-959.
-
(1988)
Brain
, vol.111
, Issue.PART 4
, pp. 941-959
-
-
Saint-Cyr, J.A.1
Taylor, A.E.2
Lang, A.E.3
-
32
-
-
77954971388
-
Abnormal explicit but normal implicit sequence learning in premanifest and early Huntington's disease
-
Schneider S.A., Wilkinson L., Bhatia K.P., Henley S.M., Rothwell J.C., Tabrizi S.J., Jahanshahi M. Abnormal explicit but normal implicit sequence learning in premanifest and early Huntington's disease. Mov. Disord. 2010, 25:1343-1349.
-
(2010)
Mov. Disord.
, vol.25
, pp. 1343-1349
-
-
Schneider, S.A.1
Wilkinson, L.2
Bhatia, K.P.3
Henley, S.M.4
Rothwell, J.C.5
Tabrizi, S.J.6
Jahanshahi, M.7
-
33
-
-
0032949459
-
A Huntington's disease CAG expansion at the murine Hdh locus is unstable and associated with behavioural abnormalities in mice
-
Shelbourne P.F., Killeen N., Hevner R.F., Johnston H.M., Tecott L., Lewandoski M., Ennis M., Ramirez L., Li Z., Iannicola C., Littman D.R., Myers R.M. A Huntington's disease CAG expansion at the murine Hdh locus is unstable and associated with behavioural abnormalities in mice. Hum. Mol. Genet. 1999, 8:763-774.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 763-774
-
-
Shelbourne, P.F.1
Killeen, N.2
Hevner, R.F.3
Johnston, H.M.4
Tecott, L.5
Lewandoski, M.6
Ennis, M.7
Ramirez, L.8
Li, Z.9
Iannicola, C.10
Littman, D.R.11
Myers, R.M.12
-
34
-
-
10744227174
-
Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease
-
Slow E.J., van Raamsdonk J., Rogers D., Coleman S.H., Graham R.K., Deng Y., Oh R., Bissada N., Hossain S.M., Yang Y.Z., Li X.J., Simpson E.M., Gutekunst C.A., Leavitt B.R., Hayden M.R. Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease. Hum. Mol. Genet. 2003, 12:1555-1567.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 1555-1567
-
-
Slow, E.J.1
van Raamsdonk, J.2
Rogers, D.3
Coleman, S.H.4
Graham, R.K.5
Deng, Y.6
Oh, R.7
Bissada, N.8
Hossain, S.M.9
Yang, Y.Z.10
Li, X.J.11
Simpson, E.M.12
Gutekunst, C.A.13
Leavitt, B.R.14
Hayden, M.R.15
-
35
-
-
0035118624
-
Longitudinal evaluation of cognitive disorder in Huntington's disease
-
Snowden J., Craufurd D., Griffiths H., Thompson J., Neary D. Longitudinal evaluation of cognitive disorder in Huntington's disease. J. Int. Neuropsychol. Soc. 2001, 7:33-44.
-
(2001)
J. Int. Neuropsychol. Soc.
, vol.7
, pp. 33-44
-
-
Snowden, J.1
Craufurd, D.2
Griffiths, H.3
Thompson, J.4
Neary, D.5
-
36
-
-
0036257088
-
Psychomotor, executive, and memory function in preclinical Huntington's disease
-
Snowden J.S., Craufurd D., Thompson J., Neary D. Psychomotor, executive, and memory function in preclinical Huntington's disease. J. Clin. Exp. Neuropsychol. 2002, 24:133-145.
-
(2002)
J. Clin. Exp. Neuropsychol.
, vol.24
, pp. 133-145
-
-
Snowden, J.S.1
Craufurd, D.2
Thompson, J.3
Neary, D.4
-
37
-
-
0028918558
-
The pattern of attentional deficits in Huntington's disease
-
Sprengelmeyer R., Lange H., Homberg V. The pattern of attentional deficits in Huntington's disease. Brain 1995, 118(Pt 1):145-152.
-
(1995)
Brain
, vol.118
, Issue.PART 1
, pp. 145-152
-
-
Sprengelmeyer, R.1
Lange, H.2
Homberg, V.3
-
38
-
-
0027480960
-
-
The Huntington's disease collaborative research group, 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. The Huntington's Disease Collaborative Research Group. Cell 1993, 72:971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
39
-
-
71849113945
-
Automaticity and attention in Huntington's disease: when two hands are not better than one
-
Thompson J.C., Poliakoff E., Sollom A.C., Howard E., Craufurd D., Snowden J.S. Automaticity and attention in Huntington's disease: when two hands are not better than one. Neuropsychologia 2010, 48:171-178.
-
(2010)
Neuropsychologia
, vol.48
, pp. 171-178
-
-
Thompson, J.C.1
Poliakoff, E.2
Sollom, A.C.3
Howard, E.4
Craufurd, D.5
Snowden, J.S.6
-
40
-
-
16244411642
-
Implicit learning in a serial choice visual discrimination task in the operant 9-hole box by intact and striatal lesioned mice
-
Trueman R.C., Brooks S.P., Dunnett S.B. Implicit learning in a serial choice visual discrimination task in the operant 9-hole box by intact and striatal lesioned mice. Behav. Brain Res. 2005, 159:313-322.
-
(2005)
Behav. Brain Res.
, vol.159
, pp. 313-322
-
-
Trueman, R.C.1
Brooks, S.P.2
Dunnett, S.B.3
-
41
-
-
33847053686
-
The operant serial implicit learning task reveals early onset motor learning deficits in the Hdh knock-in mouse model of Huntington's disease
-
Trueman R.C., Brooks S.P., Jones L., Dunnett S.B. The operant serial implicit learning task reveals early onset motor learning deficits in the Hdh knock-in mouse model of Huntington's disease. Eur. J. Neurosci. 2007, 25:551-558.
-
(2007)
Eur. J. Neurosci.
, vol.25
, pp. 551-558
-
-
Trueman, R.C.1
Brooks, S.P.2
Jones, L.3
Dunnett, S.B.4
-
42
-
-
41149153221
-
Time course of choice reaction time deficits in the Hdh (Q92) knock-in mouse model of Huntington's disease in the operant serial implicit learning task (SILT)
-
Trueman R.C., Brooks S.P., Jones L., Dunnett S.B. Time course of choice reaction time deficits in the Hdh (Q92) knock-in mouse model of Huntington's disease in the operant serial implicit learning task (SILT). Behav. Brain Res. 2008, 189:317-324.
-
(2008)
Behav. Brain Res.
, vol.189
, pp. 317-324
-
-
Trueman, R.C.1
Brooks, S.P.2
Jones, L.3
Dunnett, S.B.4
-
43
-
-
29644433445
-
Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington disease
-
Van Raamsdonk J.M., Murphy Z., Slow E.J., Leavitt B.R., Hayden M.R. Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington disease. Hum. Mol. Genet. 2005, 14:3823-3835.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 3823-3835
-
-
Van Raamsdonk, J.M.1
Murphy, Z.2
Slow, E.J.3
Leavitt, B.R.4
Hayden, M.R.5
-
44
-
-
25644445315
-
Cystamine treatment is neuroprotective in the YAC128 mouse model of Huntington disease
-
Van Raamsdonk J.M., Pearson J., Bailey C.D., Rogers D.A., Johnson G.V., Hayden M.R., Leavitt B.R. Cystamine treatment is neuroprotective in the YAC128 mouse model of Huntington disease. J. Neurochem. 2005.
-
(2005)
J. Neurochem.
-
-
Van Raamsdonk, J.M.1
Pearson, J.2
Bailey, C.D.3
Rogers, D.A.4
Johnson, G.V.5
Hayden, M.R.6
Leavitt, B.R.7
-
45
-
-
19744380273
-
Loss of wild-type huntingtin influences motor dysfunction and survival in the YAC128 mouse model of Huntington disease
-
Van Raamsdonk J.M., Pearson J., Rogers D.A., Bissada N., Vogl A.W., Hayden M.R., Leavitt B.R. Loss of wild-type huntingtin influences motor dysfunction and survival in the YAC128 mouse model of Huntington disease. Hum. Mol. Genet. 2005, 14:1379-1392.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 1379-1392
-
-
Van Raamsdonk, J.M.1
Pearson, J.2
Rogers, D.A.3
Bissada, N.4
Vogl, A.W.5
Hayden, M.R.6
Leavitt, B.R.7
-
46
-
-
17644368893
-
Cognitive dysfunction precedes neuropathology and motor abnormalities in the YAC128 mouse model of Huntington's disease
-
Van Raamsdonk J.M., Pearson J., Slow E.J., Hossain S.M., Leavitt B.R., Hayden M.R. Cognitive dysfunction precedes neuropathology and motor abnormalities in the YAC128 mouse model of Huntington's disease. J. Neurosci. 2005, 25:4169-4180.
-
(2005)
J. Neurosci.
, vol.25
, pp. 4169-4180
-
-
Van Raamsdonk, J.M.1
Pearson, J.2
Slow, E.J.3
Hossain, S.M.4
Leavitt, B.R.5
Hayden, M.R.6
-
47
-
-
0037444426
-
Transgenic rat model of Huntington's disease
-
von Horsten S., Schmitt I., Nguyen H.P., Holzmann C., Schmidt T., Walther T., Bader M., Pabst R., Kobbe P., Krotova J., Stiller D., Kask A., Vaarmann A., Rathke-Hartlieb S., Schulz J.B., Grasshoff U., Bauer I., Vieira-Saecker A.M., Paul M., Jones L., Lindenberg K.S., Landwehrmeyer B., Bauer A., Li X.J., Riess O. Transgenic rat model of Huntington's disease. Hum. Mol. Genet. 2003, 12:617-624.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 617-624
-
-
von Horsten, S.1
Schmitt, I.2
Nguyen, H.P.3
Holzmann, C.4
Schmidt, T.5
Walther, T.6
Bader, M.7
Pabst, R.8
Kobbe, P.9
Krotova, J.10
Stiller, D.11
Kask, A.12
Vaarmann, A.13
Rathke-Hartlieb, S.14
Schulz, J.B.15
Grasshoff, U.16
Bauer, I.17
Vieira-Saecker, A.M.18
Paul, M.19
Jones, L.20
Lindenberg, K.S.21
Landwehrmeyer, B.22
Bauer, A.23
Li, X.J.24
Riess, O.25
more..
-
48
-
-
0022395922
-
Neuropathological classification of Huntington's disease
-
Vonsattel J.P., Myers R.H., Stevens T.J., Ferrante R.J., Bird E.D., Richardson E.P. Neuropathological classification of Huntington's disease. J. Neuropathol. Exp. Neurol. 1985, 44:559-577.
-
(1985)
J. Neuropathol. Exp. Neurol.
, vol.44
, pp. 559-577
-
-
Vonsattel, J.P.1
Myers, R.H.2
Stevens, T.J.3
Ferrante, R.J.4
Bird, E.D.5
Richardson, E.P.6
-
49
-
-
0032938295
-
Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse
-
Wheeler V.C., Auerbach W., White J.K., Srinidhi J., Auerbach A., Ryan A., Duyao M.P., Vrbanac V., Weaver M., Gusella J.F., Joyner A.L., MacDonald M.E. Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse. Hum. Mol. Genet. 1999, 8:115-122.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 115-122
-
-
Wheeler, V.C.1
Auerbach, W.2
White, J.K.3
Srinidhi, J.4
Auerbach, A.5
Ryan, A.6
Duyao, M.P.7
Vrbanac, V.8
Weaver, M.9
Gusella, J.F.10
Joyner, A.L.11
MacDonald, M.E.12
-
50
-
-
0027301298
-
Evidence for dissociable motor skills in Huntington's disease patients
-
Willingham D.B., Koroshetz W.J. Evidence for dissociable motor skills in Huntington's disease patients. Psychobiology 1993, 21:173-182.
-
(1993)
Psychobiology
, vol.21
, pp. 173-182
-
-
Willingham, D.B.1
Koroshetz, W.J.2
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