Autosomal dominant cerebellar ataxia (SCA6): clinical, genetic and neuropathological study in a family

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Roel A. Ophoff, Gisela M. Terwindt, Monique N. Vergouwe et al. · Cell · 1996 · 2.3K citations · Full text

Channelopathies, Genetic Disorder, Genetics +5

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel

Olga Zhuchenko, Jennifer M. Bailey, Penelope E. Bonnen et al. · Nature Genetics · 1997 · 1.6K citations

Small Polyglutamine Expansions, Neurobiology Of Disease, Molecular Neuroscience +14

Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)

M Papp, J. Kahn, P. L. Lantos · Journal of the Neurological Sciences · 1989 · 976 citations

Shy-drager Syndrome, Corticobasal Degeneration, Neuroanatomy +11

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT

Kazuhiro Sanpei, Hiroki Takano, S. Igarashi et al. · Nature Genetics · 1996 · 771 citations

Molecular Neuroscience, Direct Identification, Cloning Technique +12

Clinical features and classification of inherited ataxias.

A. E. Harding · PubMed · 1993 · 424 citations

Inherited Ataxias, Neurological Disorder, Genetic Disorder +4