Spinocerebellar Ataxia Type 2 (Sca2) Associated with Retinal Pigmentary Degeneration

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies)

Alexandra Dürr, Didier Smadja, Géraldine Cancel‐Tassin et al. · Brain · 1995 · 188 citations

Neurodegenerative Diseases, Alzheimer's Disease, Ophthalmology +14

Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation

Jenni Johansson · Human Molecular Genetics · 1998 · 169 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Cag Repeats +15

Oculomotor Phenotypes in Autosomal Dominant Ataxias

Ned Buttner, Daniel H. Geschwind, Joanna C. Jen et al. · Archives of Neurology · 1998 · 165 citations

Autosomal dominant cerebellar ataxia with retinal degeneration

Launce Gouw, Kathleen B. Digre, Cheryl P. Harris et al. · Neurology · 1994 · 131 citations

Genetics, Disease Gene Identification, Genetic Analysis +16

Ocular Changes in Patients With Spinocerebellar Degeneration and Repeated Trinucleotide Expansion of Spinocerebellar Ataxia Type 1 Gene

Toshiaki Abe · Archives of Ophthalmology · 1997 · 62 citations