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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… 
Highly Cited
2007
Highly Cited
2007
Skeletal muscle atrophy is associated with a marked and sustained activation of nuclear factor-kappaB (NF-kappaB) activity… 
Highly Cited
2003
Highly Cited
2003
Leptin may influence RA in opposing ways: enhance the expression of Th1 cytokines or limit the inflammatory responses Leptin is… 
Review
1998
Review
1998
PURPOSE Retinal and choroidal changes are considered uncommon ocular complications in preeclampsia. The authors evaluated… 
Review
1998
Review
1998
Clinical revaluation and genetic analysis of six Indian pedigrees, segregating autosomal dominant cerebellar ataxia, slow… 
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
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… 
Highly Cited
1973
Highly Cited
1973
Testosterone-filled polydimethylsiloxane (PDS) capsules, ranging between 800 and 25,600 mm2 in surface area, were placed…