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Spinocerebellar Ataxia Type 2

Known as: Cerebellar Degeneration with Slow Eye Movements, Type 2 Spinocerebellar Ataxia, IIs, Spinocerebellar Atrophy 
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan Department of Retinal Disease Control… 
Review
2002
Review
2002
Mitochondrial DNA (mtDNA) deletion mutations accumulate with age in tissues of a variety of species. Although the relatively low… 
Review
1998
Review
1998
Clinical revaluation and genetic analysis of six Indian pedigrees, segregating autosomal dominant cerebellar ataxia, slow… 
Review
1998
Review
1998
PURPOSE Retinal and choroidal changes are considered uncommon ocular complications in preeclampsia. The authors evaluated… 
1995
1995
Article abstract-The gene for spinocerebellar ataxia type 2 (SCA2) is mapped to chromosome 12q23-24.1. Using D12S79 and D12S105… 
Highly Cited
1990
Highly Cited
1990
This study investigated the roles of the melatonin signal and the circadian system in the induction of photoperiodic responses in… 
Highly Cited
1979
Highly Cited
1979
One purpose of this study was to determine if pineal melatonin is altered by chronic exposure to a lighting schedule which… 
Highly Cited
1975
Highly Cited
1975
In male hamsters, light deprivation was reported to reduce both testis weight and prolactin (PRL) levels. Therefore, we decided… 
Highly Cited
1974
Highly Cited
1974
The relationship between testicular function and peripheral gonadotropin levels was investigated in adult hamsters throughout a… 
Highly Cited
1973
Highly Cited
1973
In a series of ninety-six operations for carpal-tunnel syndrome, internal neurolysis of the median nerve was done under loupe…