-
1
-
-
0027164698
-
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
-
Orr HT, Chung M, Banfi S, et al. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nature Genet 1993;4:221-226.
-
(1993)
Nature Genet
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.2
Banfi, S.3
-
2
-
-
0027162192
-
Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1
-
Gispert S, Twells R, Orozco G. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1. Nature Genet 1993;4:295-299.
-
(1993)
Nature Genet
, vol.4
, pp. 295-299
-
-
Gispert, S.1
Twells, R.2
Orozco, G.3
-
3
-
-
0027279503
-
The gene for Machado-Joseph disease maps to human chromosome 14q
-
Takiyama Y, Nishizawa M, Tanaka H, et al. The gene for Machado-Joseph disease maps to human chromosome 14q. Nature Genet 1993;4:300-304.
-
(1993)
Nature Genet
, vol.4
, pp. 300-304
-
-
Takiyama, Y.1
Nishizawa, M.2
Tanaka, H.3
-
4
-
-
0029006340
-
Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease
-
Matilla T, McCall A, Subramony SH, Zoghbi HY. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease. Ann Neurol 1995;38:68-72.
-
(1995)
Ann Neurol
, vol.38
, pp. 68-72
-
-
Matilla, T.1
McCall, A.2
Subramony, S.H.3
Zoghbi, H.Y.4
-
5
-
-
0002170153
-
La forme radiculo-cordonnale postériure des dégénérescences spino-cérébelleuses
-
Biemond A. La forme radiculo-cordonnale postériure des dégénérescences spino-cérébelleuses. Rev Neurol 1954;91:2-21.
-
(1954)
Rev Neurol
, vol.91
, pp. 2-21
-
-
Biemond, A.1
-
6
-
-
0025170522
-
Benign hereditary cerebellar ataxia with extensive thermoanalgesia
-
Pollock M, Kies B. Benign hereditary cerebellar ataxia with extensive thermoanalgesia. Brain 1990;113:857-865.
-
(1990)
Brain
, vol.113
, pp. 857-865
-
-
Pollock, M.1
Kies, B.2
-
7
-
-
0021355782
-
Large-fiber sensory neuronopathy in autosomal dominant spinocerebellar degeneration
-
Bennett RH, Ludvigson P, DeLeon G, Berry G. Large-fiber sensory neuronopathy in autosomal dominant spinocerebellar degeneration. Arch Neurol 1984;41:175-178.
-
(1984)
Arch Neurol
, vol.41
, pp. 175-178
-
-
Bennett, R.H.1
Ludvigson, P.2
DeLeon, G.3
Berry, G.4
-
8
-
-
0001172320
-
Autosomal dominant spinocerebellar ataxia: Clinical description of a distinct hereditary ataxia and genetic localization to chromosome 16 (SCA4) in a Utah kindred
-
Gardner K, Alderson K, Galster B, Kaplan C, Leppert M, Ptacek L. Autosomal dominant spinocerebellar ataxia: clinical description of a distinct hereditary ataxia and genetic localization to chromosome 16 (SCA4) in a Utah kindred [Abstract]. Neurology 1994;44:A361.
-
(1994)
Neurology
, vol.44
-
-
Gardner, K.1
Alderson, K.2
Galster, B.3
Kaplan, C.4
Leppert, M.5
Ptacek, L.6
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