-
1
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
-
Neary D, Snowden JS, Gustafson L, Passant U, Stuss D, Black S, Freedman M, Kertesz A, Robert PH, Albert M, Boone K, Miller BL, Cummings J, Benson DF: Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 1998; 51: 1546-1554.
-
(1998)
Neurology
, vol.51
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
Passant, U.4
Stuss, D.5
Black, S.6
Freedman, M.7
Kertesz, A.8
Robert, P.H.9
Albert, M.10
Boone, K.11
Miller, B.L.12
Cummings, J.13
Benson, D.F.14
-
2
-
-
0003310147
-
The frontal lobes and behaviour: Theoretical considerations; in Fronto-temporal lobar degeneration: Fronto-temporal dementia progressive aphasia semantic dementia
-
Snowden JS, Mann, DMA, Neary D: The frontal lobes and behaviour: Theoretical considerations; in Fronto-temporal lobar degeneration: fronto-temporal dementia, progressive aphasia, semantic dementia. Clinical Neurology and Neurosurgery Monographs 1996; 147-167.
-
(1996)
Clinical Neurology and Neurosurgery Monographs
, pp. 147-167
-
-
Snowden, J.S.1
Mann, D.M.A.2
Neary, D.3
-
3
-
-
0028223015
-
The lund and manchester groups: Clinical and neuropathological criteria for frontotemporal dementia
-
The Lund and Manchester Groups: Clinical and neuropathological criteria for frontotemporal dementia. J Neurol Neurosurg Psychiatry 1994; 57: 416-418.
-
(1994)
J. Neurol. Neurosurg. Psychiatry
, vol.57
, pp. 416-418
-
-
-
4
-
-
35248886083
-
Semantic dementia: A unique clinicopathological syndrome
-
DOI 10.1016/S1474-4422(07)70266-1, PII S1474442207702661
-
Hodges JR, Patterson K: Semantic dementia: A unique clinicopathological syndrome. Lancet Neurol 2007; 6: 1004-1014. (Pubitemid 47562322) (Pubitemid 47562322)
-
(2007)
Lancet Neurology
, vol.6
, Issue.11
, pp. 1004-1014
-
-
Hodges, J.R.1
Patterson, K.2
-
5
-
-
0032771614
-
Semantic dysfunction in frontotemporal lobar degeneration
-
DOI 10.1159/000051209
-
Snowden JS: Semantic dysfunction in frontotemporal lobar degeneration. Dement Geriatr Cogn Disord 1999; 10(suppl 1):33-36. (Pubitemid 29348611) (Pubitemid 29348611)
-
(1999)
Dementia and Geriatric Cognitive Disorders
, vol.10
, Issue.SUPPL. 1
, pp. 33-36
-
-
Snowden, J.S.1
-
6
-
-
1842734156
-
Knowledge of famous faces and names in semantic dementia
-
DOI 10.1093/brain/awh099
-
Snowden JS, Thompson JC, Neary D: Knowledge of famous faces and names in semantic dementia. Brain 2004; 127: 860-872. (Pubitemid 38478531) (Pubitemid 38478531)
-
(2004)
Brain
, vol.127
, Issue.4
, pp. 860-872
-
-
Snowden, J.S.1
Thompson, J.C.2
Neary, D.3
-
7
-
-
44149111570
-
Longitudinal studies of semantic dementia: The relationship between structural and functional changes over time
-
Bright P, Moss HE, Stamatakis EA, Tyler LK: Longitudinal studies of semantic dementia: The relationship between structural and functional changes over time. Neuropsychologia 2008; 46: 2177-2188.
-
(2008)
Neuropsychologia
, vol.46
, pp. 2177-2188
-
-
Bright, P.1
Moss, H.E.2
Stamatakis, E.A.3
Tyler, L.K.4
-
8
-
-
0035069988
-
Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease
-
DOI 10.1002/ana.92
-
Chan D, Fox NC, Scahill RI, Crum WR, Whitwell JL, Leschziner G, Rossor AM, Stevens JM, Cipolotti L, Rossor MN: Patterns of temporal lobe atrophy in semantic dementia and Alzheimers disease. Ann Neurol 2001; 49: 433-442. (Pubitemid 32281327) (Pubitemid 32281327)
-
(2001)
Annals of Neurology
, vol.49
, Issue.4
, pp. 433-442
-
-
Chan, D.1
Fox, N.C.2
Scahill, R.I.3
Crum, W.R.4
Whitwell, J.L.5
Leschziner, G.6
Rossor, A.M.7
Stevens, J.M.8
Cipolotti, L.9
Rossor, M.N.10
-
9
-
-
0035943005
-
Differing patterns of temporal atrophy in Alzheimer's disease and semantic dementia
-
Galton CJ, Patterson K, Graham K, Lambon- Ralph MA, Williams G, Antoun N, Sahakian BJ, Hodges JR: Differing patterns of temporal atrophy in Alzheimers disease and semantic dementia. Neurology 2001; 57: 216-225. (Pubitemid 32667354) (Pubitemid 32667354)
-
(2001)
Neurology
, vol.57
, Issue.2
, pp. 216-225
-
-
Galton, C.J.1
Patterson, K.2
Graham, K.3
Lambon-Ralph, M.A.4
Williams, G.5
Antoun, N.6
Sahakian, B.J.7
Hodges, J.R.8
-
10
-
-
0036205905
-
Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene
-
Pickering-Brown SM, Richardson AM, Snowden JS, McDonagh AM, Burns A, Braude W, Baker M, Liu WK, Yen SH, Hardy J, Hutton M, Davies Y, Allsop D, Craufurd D, Neary D, Mann DM: Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene. Brain 2002; 125: 732-751. (Pubitemid 34279770) (Pubitemid 34279770)
-
(2002)
Brain
, vol.125
, Issue.4
, pp. 732-751
-
-
Pickering-Brown, S.M.1
Richardson, A.M.T.2
Snowden, J.S.3
McDonagh, A.M.4
Burns, A.5
Braude, W.6
Baker, M.7
Liu, W.-K.8
Yen, S.-H.9
Hardy, J.10
Hutton, M.11
Davies, Y.12
Allsop, D.13
Craufurd, D.14
Neary, D.15
Mann, D.M.A.16
-
11
-
-
39749187585
-
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: Comparison with patients with MAPT and no known mutations
-
DOI 10.1093/brain/awm331
-
Pickering-Brown SM, Rollinson S, Du Plessis D, Morrison KE, Varma A, Richardson AM, Neary D, Snowden JS, Mann DM: Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: Comparison with patients with MAPT and no known mutations. Brain 2008; 131: 721-731. (Pubitemid 351294717) (Pubitemid 351294717)
-
(2008)
Brain
, vol.131
, Issue.3
, pp. 721-731
-
-
Pickering-Brown, S.M.1
Rollinson, S.2
Du Plessis, D.3
Morrison, K.E.4
Varma, A.5
Richardson, A.M.T.6
Neary, D.7
Snowden, J.S.8
Mann, D.M.A.9
-
12
-
-
24344458148
-
The pathological basis of semantic dementia
-
DOI 10.1093/brain/awh582
-
Davies RR, Hodges JR, Kril JJ, Patterson K, Halliday GM, Xuereb JH: The pathological basis of semantic dementia. Brain 2005; 128: 1984-1995. (Pubitemid 41253266) (Pubitemid 41253266)
-
(2005)
Brain
, vol.128
, Issue.9
, pp. 1984-1995
-
-
Davies, R.R.1
Hodges, J.R.2
Kril, J.J.3
Patterson, K.4
Halliday, G.M.5
Xuereb, J.H.6
-
14
-
-
34447099564
-
Frontotemporal lobar degeneration: Clinical and pathological relationships
-
DOI 10.1007/s00401-007-0236-3
-
Snowden J, Neary D, Mann D: Frontotemporal lobar degeneration: Clinical and pathological relationships. Acta Neuropathol 2007; 114: 31-38. (Pubitemid 47029057) (Pubitemid 47029057)
-
(2007)
Acta Neuropathologica
, vol.114
, Issue.1
, pp. 31-38
-
-
Snowden, J.1
Neary, D.2
Mann, D.3
-
15
-
-
74249101783
-
Semantic dementia: Demography familial factors and survival in a consecutive series of 100 cases
-
Hodges JR, Mitchell J, Dawson K, Spillantini MG, Xuereb JH, McMonagle P, Nestor PJ, Patterson K: Semantic dementia: demography, familial factors and survival in a consecutive series of 100 cases. Brain 2010; 133: 300-306.
-
(2010)
Brain
, vol.133
, pp. 300-306
-
-
Hodges, J.R.1
Mitchell, J.2
Dawson, K.3
Spillantini, M.G.4
Xuereb, J.H.5
McMonagle, P.6
Nestor, P.J.7
Patterson, K.8
-
16
-
-
57049105123
-
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: Consensus recommendations
-
Mackenzie IR, Neumann M, Bigio EH, Cairns NJ, Alafuzoff I, Kril J, Kovacs GG, Ghetti B, Halliday G, Holm IE, Ince PG, Kamphorst W, Revesz T, Rozemuller AJ, Kumar- Singh S, Akiyama H, Baborie A, Spina S, Dickson DW, Trojanowski JQ, Mann DM: Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: Consensus recommendations. Acta Neuropathol 2009; 117: 15-18.
-
(2009)
Acta. Neuropathol.
, vol.117
, pp. 15-18
-
-
Mackenzie, I.R.1
Neumann, M.2
Bigio, E.H.3
Cairns, N.J.4
Alafuzoff, I.5
Kril, J.6
Kovacs, G.G.7
Ghetti, B.8
Halliday, G.9
Holm, I.E.10
Ince, P.G.11
Kamphorst, W.12
Revesz, T.13
Rozemuller, A.J.14
Kumar- Singh, S.15
Akiyama, H.16
Baborie, A.17
Spina, S.18
Dickson, D.W.19
Trojanowski, J.Q.20
Mann, D.M.21
more..
-
17
-
-
77649187519
-
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: An update
-
Mackenzie IR, Neumann M, Bigio EH, Cairns NJ, Alafuzoff I, Kril J, Kovacs GG, Ghetti B, Halliday G, Holm IE, Ince PG, Kamphorst W, Revesz T, Rozemuller AJ, Kumar- Singh S, Akiyama H, Baborie A, Spina S, Dickson DW, Trojanowski JQ, Mann DM: Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update. Acta Neuropathol 2010; 119: 1-4.
-
(2010)
Acta. Neuropathol.
, vol.119
, pp. 1-4
-
-
Mackenzie, I.R.1
Neumann, M.2
Bigio, E.H.3
Cairns, N.J.4
Alafuzoff, I.5
Kril, J.6
Kovacs, G.G.7
Ghetti, B.8
Halliday, G.9
Holm, I.E.10
Ince, P.G.11
Kamphorst, W.12
Revesz, T.13
Rozemuller, A.J.14
Kumar- Singh, S.15
Akiyama, H.16
Baborie, A.17
Spina, S.18
Dickson, D.W.19
Trojanowski, J.Q.20
Mann, D.M.21
more..
-
18
-
-
0010991122
-
Manual for the wechsler adult intelligence scale - Revised
-
Wechsler D ed New York
-
Wechsler D (ed): Manual for the Wechsler Adult Intelligence Scale - Revised. New York, The Psychological Corporation, 1981.
-
(1981)
Psychological Corporation
-
-
-
19
-
-
0031768638
-
Prospective and retrospective studies of recovery in aphasia. Changes in cerebral blood flow and language functions
-
DOI 10.1093/brain/121.11.2083
-
Mimura M, Kato M, Sano Y, Kojima T, Naeser M, Kashima H: Prospective and retrospective studies of recovery in aphasia. Changes in cerebral blood flow and language functions. Brain 1998; 121: 2083-2094. (Pubitemid 28497906) (Pubitemid 28497906)
-
(1998)
Brain
, vol.121
, Issue.11
, pp. 2083-2094
-
-
Mimura, M.1
Kato, M.2
Kato, M.3
Sano, Y.4
Kojima, T.5
Naeser, M.6
Kashima, H.7
-
20
-
-
0003690749
-
Trail making test: Manual for administration and scoring
-
Reitan RM ed
-
Reitan RM (ed): Trail Making Test: Manual for Administration and Scoring. Tucson, Reitan Neuropsychology Laboratory, 1992.
-
(1992)
Tucson Reitan Neuropsychology Laboratory
-
-
-
21
-
-
35648981928
-
Clinical and molecular genetic assessment of a chorea-acanthocytosis pedigree
-
DOI 10.1016/j.jns.2007.07.011, PII S0022510X07004674
-
Ichiba M, Nakamura M, Kusumoto A, Mizuno E, Kurano Y, Matsuda M, Kato M, Agemura A, Tomemori Y, Muroya S, Nakabeppu Y, Sano A: Clinical and molecular genetic assessment of a chorea-acanthocytosis pedigree. J Neurol Sci 2007; 263: 124-132. (Pubitemid 350029852) (Pubitemid 350029852)
-
(2007)
Journal of the Neurological Sciences
, vol.263
, Issue.1-2
, pp. 124-132
-
-
Ichiba, M.1
Nakamura, M.2
Kusumoto, A.3
Mizuno, E.4
Kurano, Y.5
Matsuda, M.6
Kato, M.7
Agemura, A.8
Tomemori, Y.9
Muroya, S.10
Nakabeppu, Y.11
Sano, A.12
-
22
-
-
0004810457
-
A corrected table for determining the significance of the difference between verbal and performance IQs on the wais and the wechsler-bellevue
-
Fisher GM: A corrected table for determining the significance of the difference between verbal and performance IQ's on the WAIS and the Wechsler-Bellevue. J Clin Psychol 1960; 16: 7-8.
-
(1960)
J. Clin. Psychol.
, vol.16
, pp. 7-8
-
-
Fisher, G.M.1
-
23
-
-
34547661737
-
Evaluation of brain perfusion SPECT using an easy Z-score imaging system (eZIS) as an adjunct to early-diagnosis of neurodegenerative diseases
-
DOI 10.1016/j.jns.2007.03.027, PII S0022510X07002699
-
Waragai M, Yamada T, Matsuda H: Evaluation of brain perfusion spect using an easy z-score imaging system (EZIS) as an adjunct to early-diagnosis of neurodegenerative diseases. J Neurol Sci 2007; 260: 57-64. (Pubitemid 47212200) (Pubitemid 47212200)
-
(2007)
Journal of the Neurological Sciences
, vol.260
, Issue.1-2
, pp. 57-64
-
-
Waragai, M.1
Yamada, T.2
Matsuda, H.3
-
24
-
-
0033041179
-
Association of an extended haplotype in the tau gene with progressive supranuclear palsy
-
Baker M, Litvan I, Houlden H, Adamson J, Dickson D, Perez-Tur J, Hardy J, Lynch T, Bigio E, Hutton M: Association of an extended haplotype in the tau gene with progressive supranuclear palsy. Hum Mol Genet 1999; 8: 711-715. (Pubitemid 29139987) (Pubitemid 29139987)
-
(1999)
Human Molecular Genetics
, vol.8
, Issue.4
, pp. 711-715
-
-
Baker, M.1
Litvan, I.2
Houlden, H.3
Adamson, J.4
Dickson, D.5
Perez-Tur, J.6
Hardy, J.7
Lynch, T.8
Bigio, E.9
Hutton, M.10
-
25
-
-
0029896202
-
A simple and efficient method for apolipoprotein E genotype determination
-
Chapman J, Estupinan J, Asherov A, Goldfarb LG: A simple and efficient method for apolipoprotein e genotype determination. Neurology 1996; 46: 1484-1485. (Pubitemid 26159322) (Pubitemid 26159322)
-
(1996)
Neurology
, vol.46
, Issue.5
, pp. 1484-1485
-
-
Chapman, J.1
Estupinan, J.2
Asherov, A.3
Goldfarb, L.G.4
-
26
-
-
33746196787
-
The H2 MAPT haplotype is associated with familial frontotemporal dementia
-
DOI 10.1016/j.nbd.2005.11.013, PII S0969996105003189
-
Ghidoni R, Signorini S, Barbiero L, Sina E, Cominelli P, Villa A, Benussi L, Binetti G: The H2 MAPT haplotype is associated with familial frontotemporal dementia. Neurobiol Dis 2006; 22: 357-362. (Pubitemid 44294282) (Pubitemid 44294282)
-
(2006)
Neurobiology of Disease
, vol.22
, Issue.2
, pp. 357-362
-
-
Ghidoni, R.1
Signorini, S.2
Barbiero, L.3
Sina, E.4
Cominelli, P.5
Villa, A.6
Benussi, L.7
Binetti, G.8
-
27
-
-
0034971707
-
Missense and splice site mutations in tau associated with FTDP-17: Multiple pathogenic mechanisms
-
Hutton M: Missense and splice site mutations in tau associated with FTDP-17: multiple pathogenic mechanisms. Neurology 2001; 56:S21-S25. (Pubitemid 32539643) (Pubitemid 32539643)
-
(2001)
Neurology
, vol.56
, Issue.11 SUPPL. 4
-
-
Hutton, M.1
-
28
-
-
0030977392
-
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference
-
DOI 10.1002/ana.410410606
-
Foster NL, Wilhelmsen K, Sima AA, Jones MZ, D'Amato CJ, Gilman S: Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference participants. Ann Neurol 1997; 41: 706-715. (Pubitemid 27249175) (Pubitemid 27249175)
-
(1997)
Annals of Neurology
, vol.41
, Issue.6
, pp. 706-715
-
-
Foster, N.L.1
Wilhelmsen, K.2
Sima, A.A.F.3
Jones, M.Z.4
D'Amato, C.J.5
Gilman, S.6
-
29
-
-
0031045491
-
Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: A genetic and clinicopathological study of three Dutch families
-
DOI 10.1002/ana.410410205
-
Heutink P, Stevens M, Rizzu P, Bakker E, Kros JM, Tibben A, Niermeijer MF, van Duijn CM, Oostra BA, van Swieten JC: Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three dutch families. Ann Neurol 1997; 41: 150-159. (Pubitemid 27082095) (Pubitemid 27082095)
-
(1997)
Annals of Neurology
, vol.41
, Issue.2
, pp. 150-159
-
-
Heutink, P.1
Stevens, M.2
Rizzu, P.3
Bakker, E.4
Kros, J.M.5
Tibben, A.6
Niermeijer, M.F.7
Van Duijn, C.M.8
Oostra, B.A.9
Van Swieten, J.C.10
-
30
-
-
0032543684
-
Association of missense and 5-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, Petersen RC, Stevens M, de Graaff E, Wauters E, van Baren J, Hillebrand M, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA, Trojanowski J, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, Dodd PR, Hayward N, Kwok JB,Schofield PR, Andreadis A, Snowden J, Craufurd D, Neary D, Owen F, Oostra BA, Hardy J, Goate A, van Swieten J, Mann D, Lynch T, Heutink P: Association of missense and 5-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 1998; 393: 702-705.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
Baker, M.4
Froelich, S.5
Houlden, H.6
Pickering-Brown, S.7
Chakraverty, S.8
Isaacs, A.9
Grover, A.10
Hackett, J.11
Adamson, J.12
Lincoln, S.13
Dickson, D.14
Davies, P.15
Petersen, R.C.16
Stevens, M.17
De Graaff, E.18
Wauters, E.19
Van Baren, J.20
Hillebrand, M.21
Joosse, M.22
Kwon, J.M.23
Nowotny, P.24
Che, L.K.25
Norton, J.26
Morris, J.C.27
Reed, L.A.28
Trojanowski, J.29
Basun, H.30
Lannfelt, L.31
Neystat, M.32
Fahn, S.33
Dark, F.34
Tannenberg, T.35
Dodd, P.R.36
Hayward, N.37
Kwok, J.B.38
Schofield, P.R.39
Andreadis, A.40
Snowden, J.41
Craufurd, D.42
Neary, D.43
Owen, F.44
Oostra, B.A.45
Hardy, J.46
Goate, A.47
Van Swieten, J.48
Mann, D.49
Lynch, T.50
Heutink, P.51
more..
-
31
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
DOI 10.1002/ana.410430617
-
Poorkaj P, Bird TD, Wijsman E, Nemens E, Garruto RM, Anderson L, Andreadis A, Wiederholt WC, Raskind M, Schellenberg GD: Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann Neurol 1998; 43: 815-825. (Pubitemid 28280226) (Pubitemid 28280226)
-
(1998)
Annals of Neurology
, vol.43
, Issue.6
, pp. 815-825
-
-
Poorkaj, P.1
Bird, T.D.2
Wijsman, E.3
Nemens, E.4
Garruto, R.M.5
Anderson, L.6
Andreadis, A.7
Wiederholt, W.C.8
Raskind, M.9
Schellenberg, G.D.10
-
32
-
-
0032560487
-
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
-
DOI 10.1073/pnas.95.13.7737
-
Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B: Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc Natl Acad Sci USA 1998; 95: 7737-7741. (Pubitemid 28293323) (Pubitemid 28293323)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.13
, pp. 7737-7741
-
-
Spillantini, M.G.1
Murrell, J.R.2
Goedert, M.3
Farlow, M.R.4
Klug, A.5
Ghetti, B.6
-
33
-
-
33847103297
-
Frontotemporal dementia and parkinsonism linked to chromosome 17 FTDP-17
-
Wszolek ZK, Tsuboi Y, Ghetti B, Pickering- Brown S, Baba Y, Cheshire WP: Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Orphanet J Rare Dis 2006; 1: 30.
-
(2006)
Orphanet J. Rare Dis.
, vol.1
, pp. 30
-
-
Wszolek, Z.K.1
Tsuboi, Y.2
Ghetti, B.3
Pickering- Brown, S.4
Baba, Y.5
Cheshire, W.P.6
-
34
-
-
0345561533
-
Polymerization of tau peptides into fibrillar structures. The effect of FTDP-17 mutations
-
DOI 10.1016/S0014-5793(99)00210-0, PII S0014579399002100
-
Arrasate M, Perez M, Armas-Portela R, Avila J: Polymerization of tau peptides into fibrillar structures. The effect of FTDP-17 mutations. FEBS Lett 1999; 446: 199-202. (Pubitemid 29127276) (Pubitemid 29127276)
-
(1999)
FEBS Letters
, vol.446
, Issue.1
, pp. 199-202
-
-
Arrasate, M.1
Perez, M.2
Armas-Portela, R.3
Avila, J.4
-
35
-
-
68149108192
-
Familial aggregation of parkinsonism in progressive supranuclear palsy
-
Donker Kaat L, Boon AJ, Azmani A, Kamphorst W, Breteler MM, Anar B, Heutink P, van Swieten JC: Familial aggregation of parkinsonism in progressive supranuclear palsy. Neurology 2009; 73: 98-105.
-
(2009)
Neurology
, vol.73
, pp. 98-105
-
-
Donker Kaat, L.1
Boon, A.J.2
Azmani, A.3
Kamphorst, W.4
Breteler, M.M.5
Anar, B.6
Heutink, P.7
Van Swieten, J.C.8
-
36
-
-
0035954364
-
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
-
Houlden H, Baker M, Morris HR, MacDonald N, Pickering-Brown S, Adamson J, Lees AJ, Rossor MN, Quinn NP, Kertesz A, Khan MN, Hardy J, Lantos PL, St George-Hyslop P, Munoz DG, Mann D, Lang AE, Bergeron C, Bigio EH, Litvan I, Bhatia KP, Dickson D, Wood NW, Hutton M: Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype. Neurology 2001; 56: 1702-1706. (Pubitemid 32574570) (Pubitemid 32574570)
-
(2001)
Neurology
, vol.56
, Issue.12
, pp. 1702-1706
-
-
Houlden, H.1
Baker, M.2
Morris, H.R.3
MacDonald, N.4
Pickering-Brown, S.5
Adamson, J.6
Lees, A.J.7
Rossor, M.N.8
Quinn, N.P.9
Kertesz, A.10
Khan, M.N.11
Hardy, J.12
Lantos, P.L.13
St. George-Hyslop, P.14
Munoz, D.G.15
Mann, D.16
Lang, A.E.17
Bergeron, C.18
Bigio, E.H.19
Litvan, I.20
Bhatia, K.P.21
Dickson, D.22
Wood, N.W.23
Hutton, M.24
more..
-
37
-
-
0036589893
-
Further extension of the H1 haplotype associated with progressive supranuclear palsy
-
DOI 10.1002/mds.10076
-
Pastor P, Ezquerra M, Tolosa E, Munoz E, Marti MJ, Valldeoriola F, Molinuevo JL, Calopa M, Oliva R: Further extension of the H1 haplotype associated with progressive supranuclear palsy. Mov Disord 2002; 17: 550-556. (Pubitemid 36040971) (Pubitemid 36040971)
-
(2002)
Movement Disorders
, vol.17
, Issue.3
, pp. 550-556
-
-
Pastor, P.1
Ezquerra, M.2
Tolosa, E.3
Munoz, E.4
Marti, M.J.5
Valleoriola, F.6
Molinuevo, J.L.7
Calopa, M.8
Oliva, R.9
-
38
-
-
0038665270
-
Novel tau polymorphisms, tau haplotypes, and splicing in familial and sporadic frontotemporal dementia
-
DOI 10.1001/archneur.60.5.698
-
Sobrido MJ, Miller BL, Havlioglu N, Zhukareva V, Jiang Z, Nasreddine ZS, Lee VM, Chow TW, Wilhelmsen KC, Cummings JL, Wu JY, Geschwind DH: Novel tau polymorphisms, tau haplotypes, and splicing in familial and sporadic frontotemporal dementia. Arch Neurol 2003; 60: 698-702. (Pubitemid 36569887) (Pubitemid 36569887)
-
(2003)
Archives of Neurology
, vol.60
, Issue.5
, pp. 698-702
-
-
Sobrido, M.-J.1
Miller, B.L.2
Havlioglu, N.3
Zhukareva, V.4
Jiang, Z.5
Nasreddine, Z.S.6
Lee, V.M.-Y.7
Chow, T.W.8
Wilhelmsen, K.C.9
Cummings, J.L.10
Wu, J.Y.11
Geschwind, D.H.12
-
39
-
-
0036283019
-
Association between the extended tau haplotype and frontotemporal dementia
-
Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois , Didic M, Michel BF, Lacomblez L, Moreaud O, Sellal F, Golfier V, Campion D, Clerget-Darpoux F, Brice A: Association between the extended tau haplotype and frontotemporal dementia. Arch Neurol 2002; 59: 935-939. (Pubitemid 34640753) (Pubitemid 34640753)
-
(2002)
Archives of Neurology
, vol.59
, Issue.6
, pp. 935-939
-
-
Verpillat, P.1
Camuzat, A.2
Hannequin, D.3
Thomas-Anterion, C.4
Puel, M.5
Belliard, S.6
Dubois, B.7
Didic, M.8
Michel, B.-F.9
Lacomblez, L.10
Moreaud, O.11
Sellal, F.12
Golfier, V.13
Campion, D.14
Clerget-Darpoux, F.15
Brice, A.16
-
40
-
-
59649086176
-
Molecular neuropathology of TDP-43 proteinopathies
-
Neumann M: Molecular neuropathology of TDP-43 proteinopathies. Int J Mol Sci 2009; 10: 232-246.
-
(2009)
Int. J. Mol. Sci.
, vol.10
, pp. 232-246
-
-
Neumann, M.1
-
41
-
-
33749668518
-
Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: Classification and relation to clinical phenotype
-
DOI 10.1007/s00401-006-0138-9
-
Mackenzie IR, Baborie A, Pickering-Brown S, Du Plessis D, Jaros E, Perry RH, Neary D, Snowden JS, Mann DM: Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: Classification and relation to clinical phenotype. Acta Neuropathol 2006; 112: 539-549. (Pubitemid 44550678) (Pubitemid 44550678)
-
(2006)
Acta Neuropathologica
, vol.112
, Issue.5
, pp. 539-549
-
-
Mackenzie, I.R.A.1
Baborie, A.2
Pickering-Brown, S.3
Plessis, D.D.4
Jaros, E.5
Perry, R.H.6
Neary, D.7
Snowden, J.S.8
Mann, D.M.A.9
-
42
-
-
77956882625
-
Semantic dementia associated with mutation V363I in the tau gene
-
Bessi V, Bagnoli S, Nacmias B, Tedde A, Sorbi S, Bracco L: Semantic dementia associated with mutation V363I in the tau gene. J Neurol Sci 2010; 296: 112-114.
-
(2010)
J. Neurol. Sci.
, vol.296
, pp. 112-114
-
-
Bessi, V.1
Bagnoli, S.2
Nacmias, B.3
Tedde, A.4
Sorbi, S.5
Bracco, L.6
-
43
-
-
34548288059
-
Progressive nonfluent aphasia associated with a new mutation V363I in tau gene
-
DOI 10.1177/1533317507302320
-
Munoz DG, Ros R, Fatas M, Bermejo F, de Yebenes JG: Progressive nonfluent aphasia associated with a new mutation V363I in tau gene. Am J Alzheimers Dis Other Demen 2007; 22: 294-299. (Pubitemid 47330149) (Pubitemid 47330149)
-
(2007)
American Journal of Alzheimer's Disease and other Dementias
, vol.22
, Issue.4
, pp. 294-299
-
-
Munoz, D.G.1
Ros, R.2
Fatas, M.3
Bermejo, F.4
De Yebenes, J.G.5
-
44
-
-
79952194748
-
MAPT V363I variation in a sporadic case of frontotemporal dementia: Variable penetrant mutation or rare polymorphism
-
Anfossi M, Bernardi L, Gallo M, Geracitano S, Colao R, Puccio G, Curcio SAM, Frangipane F, Mirabelli M, Tomaino C, Smirne N, Maletta R, Bruni AC: MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism? Alzheimer Dis Assoc Disord 2011; 25: 96-99.
-
(2011)
Alzheimer Dis. Assoc. Disord.
, vol.25
, pp. 96-99
-
-
Anfossi, M.1
Bernardi, L.2
Gallo, M.3
Geracitano, S.4
Colao, R.5
Puccio, G.6
Curcio, S.A.M.7
Frangipane, F.8
Mirabelli, M.9
Tomaino, C.10
Smirne, N.11
Maletta, R.12
Bruni, A.C.13
|