-
1
-
-
0004160792
-
The hereditary ataxias and related disorders
-
Edinburgh: Churchill Livingstone
-
Harding AE. The hereditary ataxias and related disorders. Edinburgh: Churchill Livingstone; 1984.
-
(1984)
-
-
Harding, A.E.1
-
2
-
-
77957183085
-
Olivopontocerebellar atrophy
-
Critchley M, Greenfield JG. Olivopontocerebellar atrophy. Brain 1948;71:343-361.
-
(1948)
Brain
, vol.71
, pp. 343-361
-
-
Critchley, M.1
Greenfield, J.G.2
-
3
-
-
0004184723
-
The spinocerebellar degenerations
-
Oxford: Black-well Scientific
-
Greenfield JG. The spinocerebellar degenerations. Oxford: Black-well Scientific; 1954.
-
(1954)
-
-
Greenfield, J.G.1
-
4
-
-
0000074368
-
Olivo-ponto-cerebellar atrophy (Dejerine-Thomas type)
-
Vinken PJ, Brayen GW, editors. Amsterdam: North Holland Publishing Co
-
Eadie MJ. Olivo-ponto-cerebellar atrophy (Dejerine-Thomas type). In: Vinken PJ, Brayen GW, editors. Handbook of clinical neurology. Vol. 21. Amsterdam: North Holland Publishing Co; 1975. p 415-431.
-
(1975)
Handbook of Clinical Neurology
, vol.21
, pp. 415-431
-
-
Eadie, M.J.1
-
5
-
-
0033811949
-
Genetic background of apparently sporadic cerebellar ataxia
-
Schols L, Szymanski S, Peters S, et al. Genetic background of apparently sporadic cerebellar ataxia. Hum Genet 2000;107:132-137.
-
(2000)
Hum. Genet.
, vol.107
, pp. 132-137
-
-
Schols, L.1
Szymanski, S.2
Peters, S.3
-
6
-
-
0036238233
-
The aetiology of sporadic adult-onset ataxia
-
Abele M, Burk K, Schols L, et al. The aetiology of sporadic adult-onset ataxia. Brain 2002;125:961-968.
-
(2002)
Brain
, vol.125
, pp. 961-968
-
-
Abele, M.1
Burk, K.2
Schols, L.3
-
7
-
-
0031976207
-
Tbe cerebellar cognitive affective syndrome
-
Schmahmann JD, Sherman JC. Tbe cerebellar cognitive affective syndrome. Brain 1998;121:561-579.
-
(1998)
Brain
, vol.121
, pp. 561-579
-
-
Schmahmann, J.D.1
Sherman, J.C.2
-
8
-
-
0027437218
-
Cognitive and language functions of the human cerebellum
-
Leiner HC, Leiner AL, Dow RS. Cognitive and language functions of the human cerebellum. Trends Neurosci 1993;16:444-447.
-
(1993)
Trends Neurosci.
, vol.16
, pp. 444-447
-
-
Leiner, H.C.1
Leiner, A.L.2
Dow, R.S.3
-
9
-
-
0027286045
-
Thalamotomy for the alleviation of levodopa-induced dyskinesia: Experimental studies in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated parkinsonian monkey
-
Page RD, Sambrook MA, Crossman AR. Thalamotomy for the alleviation of levodopa-induced dyskinesia: experimental studies in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated parkinsonian monkey. Neuroscience 1993;55:147-165.
-
(1993)
Neuroscience
, vol.55
, pp. 147-165
-
-
Page, R.D.1
Sambrook, M.A.2
Crossman, A.R.3
-
10
-
-
0019484086
-
'Idiopathic' late onset cerebellar ataxia. A clinical and genetic study of 36 cases
-
Harding AE. 'Idiopathic' late onset cerebellar ataxia. A clinical and genetic study of 36 cases. J Neurol Sci 1981;51:259-271.
-
(1981)
J. Neurol. Sci.
, vol.51
, pp. 259-271
-
-
Harding, A.E.1
-
12
-
-
0027930620
-
Clinical features and natural history of multiple system atrophy. An analysis of 100 cases
-
Wenning GK, Ben Sholomo Y, Magaldaes M, Daniel SE, Quinn NP. Clinical features and natural history of multiple system atrophy. An analysis of 100 cases. 1994;117:835-845.
-
(1994)
, vol.117
, pp. 835-845
-
-
Wenning, G.K.1
Ben Sholomo, Y.2
Magaldaes, M.3
Daniel, S.E.4
Quinn, N.P.5
-
13
-
-
0029004076
-
Multiple systems atrophy and nonfamilial olivopontocerebellar atrophy are the same disease
-
Penney JB. Multiple systems atrophy and nonfamilial olivopontocerebellar atrophy are the same disease. Ann Neurol 1995;37:553-554.
-
(1995)
Ann. Neurol.
, vol.37
, pp. 553-554
-
-
Penney, J.B.1
-
14
-
-
0029942905
-
The relationship of multiple system atrophy to sporadic olivopontocerebellar atrophy and other forms of idiopathic late-onset cerebellar atrophy
-
Gilman S, Quinn NP. The relationship of multiple system atrophy to sporadic olivopontocerebellar atrophy and other forms of idiopathic late-onset cerebellar atrophy. Neurology 1996;46:1197-1199.
-
(1996)
Neurology
, vol.46
, pp. 1197-1199
-
-
Gilman, S.1
Quinn, N.P.2
-
15
-
-
0033837087
-
Evolution of sporadic olivopontocerebellar atrophy into multiple system atrophy
-
Gilman S, Little R, Johanns J, Heumann M, Kluin KJ, Junck L, Koeppe RA, An H. Evolution of sporadic olivopontocerebellar atrophy into multiple system atrophy. Neurology 2000;55:527-532.
-
(2000)
Neurology
, vol.55
, pp. 527-532
-
-
Gilman, S.1
Little, R.2
Johanns, J.3
Heumann, M.4
Kluin, K.J.5
Junck, L.6
Koeppe, R.A.7
An, H.8
-
16
-
-
0001614829
-
De l'atrophie cerebelleuse tardive a predominance corticale
-
849-885
-
Marie P, Foix C, Alajouanine T. De l'atrophie cerebelleuse tardive a predominance corticale. Rev Neurol 1922;38:849-885, 1082-1111.
-
(1922)
Rev. Neurol.
, vol.38
, pp. 1082-1111
-
-
Marie, P.1
Foix, C.2
Alajouanine, T.3
-
17
-
-
0346240996
-
Familial degeneration of the cerebellum in association with epilepsy
-
Thorpe FT. Familial degeneration of the cerebellum in association with epilepsy. Brain 1935;58:97-114.
-
(1935)
Brain
, vol.58
, pp. 97-114
-
-
Thorpe, F.T.1
-
18
-
-
0000449664
-
Hereditary form of primary parenchymatous atrophy of the cerebellar cortex associated with mental deterioration
-
Akelaitis AJ. Hereditary form of primary parenchymatous atrophy of the cerebellar cortex associated with mental deterioration. Am J Psychiatry 1938;94:1115-1140.
-
(1938)
Am. J. Psychiatry
, vol.94
, pp. 1115-1140
-
-
Akelaitis, A.J.1
-
19
-
-
84934730360
-
Familial cerebello-olivary degeneration with late development of rigidity and dementia
-
Carter HR, Sukavajana C. Familial cerebello-olivary degeneration with late development of rigidity and dementia. Neurology 1956; 6:876-884.
-
(1956)
Neurology
, vol.6
, pp. 876-884
-
-
Carter, H.R.1
Sukavajana, C.2
-
20
-
-
0348131893
-
Familial cortical cerebellar atrophy
-
Hall B, Noad KB, Latham O. Familial cortical cerebellar atrophy. Brain 1941;64:178-194.
-
(1941)
Brain
, vol.64
, pp. 178-194
-
-
Hall, B.1
Noad, K.B.2
Latham, O.3
-
22
-
-
0028859878
-
Autosomal dominant cerebellar phenotypes: The genotype has settled the phenotype
-
Rosenberg RN. Autosomal dominant cerebellar phenotypes: the genotype has settled the phenotype. Neurology 1995;45:1-5.
-
(1995)
Neurology
, vol.45
, pp. 1-5
-
-
Rosenberg, R.N.1
-
23
-
-
0029882009
-
Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-1, Machado-Joseph disease or dentaterubro-pallido-luysian atrophy locus
-
Subramony SH, Fratkin JD, Manyam VV, et al. Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-1, Machado-Joseph disease or dentaterubro-pallido-luysian atrophy locus. Mov Disord 1996;11:174-180.
-
(1996)
Mov. Disord.
, vol.11
, pp. 174-180
-
-
Subramony, S.H.1
Fratkin, J.D.2
Manyam, V.V.3
-
24
-
-
0031454530
-
Spinocerebellar ataxia type 6:Gaze evoked and vertical nystagmus, Purkinje cell degeneration and variable age of onset
-
Gomez CM, Thompson RM, Gammack JT, et al. Spinocerebellar ataxia type 6:Gaze evoked and vertical nystagmus, Purkinje cell degeneration and variable age of onset. Ann Neurol 1997;42:933-950.
-
(1997)
Ann. Neurol.
, vol.42
, pp. 933-950
-
-
Gomez, C.M.1
Thompson, R.M.2
Gammack, J.T.3
-
25
-
-
0348131892
-
CAG repeat in SCA 6
-
Zoghbi HY. CAG repeat in SCA 6. Neurology 1997;49:1197-1199.
-
(1997)
Neurology
, vol.49
, pp. 1197-1199
-
-
Zoghbi, H.Y.1
-
26
-
-
0027164698
-
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
-
Orr HT, Chung M-Y, Banfi S, et al. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet 1993;4:221-226.
-
(1993)
Nat. Genet.
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.-Y.2
Banfi, S.3
-
27
-
-
0030292488
-
Moderate expansion of normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
-
Pulst S-M. Nechiporuk A, Nechiporuk T, et al. Moderate expansion of normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nat Genet 1996;14:269-275.
-
(1996)
Nat. Genet.
, vol.14
, pp. 269-275
-
-
Pulst, S.-M.1
Nechiporuk, A.2
Nechiporuk, T.3
-
29
-
-
0014787658
-
The olivopontocerebellar atrophies: A review
-
Konigsmark BW, Weiner LP. The olivopontocerebellar atrophies: a review. Medicine 1970;49:227-241.
-
(1970)
Medicine
, vol.49
, pp. 227-241
-
-
Konigsmark, B.W.1
Weiner, L.P.2
-
30
-
-
0031659271
-
Transgenic mice in the study of polyglutamine repeat expansion diseases
-
Bates GP, Mangiarini L, Davies SW. Transgenic mice in the study of polyglutamine repeat expansion diseases. Brain Pathol 1998;8: 699-714.
-
(1998)
Brain. Pathol.
, vol.8
, pp. 699-714
-
-
Bates, G.P.1
Mangiarini, L.2
Davies, S.W.3
|