pallidoluysian atrophy
National Institutes of Health
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Spinocerebellar ataxia type 14 (SCA14; Online Mendelian Inheritance in Man, OMIM #605361) is an autosomal dominant…
Background: The prevalence of disease subtypes of spinocerebellar degenerations (SCDs) varies between countries, and even between…
Dentatorubral pallidoluysian atrophy is a neurodegenerative disease that generally presents in adulthood. Although rare, it can…
A 48‐year‐old man developed progressive hemidystonia and postural impairment with falls, followed by choreoathetosis…
Advances in molecular biology and genetics have allowed researchers to probe function and dysfunction at the level of the…
Anticipation is the clinical phenomenon in which disease onset becomes progressively earlier with increasing severity in…
Editor,—Dentatorubral and pallidoluysian atrophy (DRPLA) is an autosomal dominant disorder that manifests in a combination of…
We have systematically isolated and characterized DNA containing large CTG (n>7) repeats from a human cosmid genomic DNA library…
Abstract Dentatorubral pallidoluysian atrophy (DRPLA) is an autosomal dominant neurodegenerative disorder caused by expansion of…
Dentatorubral and pallidoluysian atrophy (DRPLA) is an autosomal dominant neurodegenerative disorder. An expanded CAG…