Dentatorubral‐pallidoluysian atrophy: Clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

1993 • 7,941 citations

Handbook of clinical neurology

1975 • 1,642 citations

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1

1993 • 1,596 citations

Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)

1994 • 1,122 citations

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

1993 • 1,084 citations

Trinucleotide repeat length instability and age of onset in Huntington's disease

1993 • 1,062 citations

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

1994 • 721 citations

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

1993 • 692 citations

A Worldwide Study of the Huntington's Disease Mutation: The Sensitivity and Specificity of Measuring CAG Repeats

1994 • 571 citations

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I

1993 • 473 citations

Homozygotes for Huntington's disease

1987 • 356 citations

Familial myoclonus epilepsy and choreoathetosis

1982 • 288 citations

Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15

1993 • 231 citations

The Haw River Syndrome: Dentatorubropallidoluysian atrophy (DRPLA) in an African–American family

1994 • 214 citations

Novel Triplet Repeat Containing Genes in Human Brain: Cloning, Expression, and Length Polymorphisms

1993 • 210 citations

Mitotic stability and meiotic variability of the (CAG)_n repeat in the Huntington disease gene

1993 • 163 citations

Molecular Genetics of Huntington's Disease

1993 • 145 citations

Hereditary dentatorubral‐pallidoluysian atrophy

1988 • 118 citations

Dentato-rubro-pallido-luysian atrophy: a clinico-pathological study.

1984 • 110 citations

Trinucleotide repeat elongation in the Huntingtin gene in Huntington Disease patients from 71 Danish families

1993 • 89 citations

HEREDO-DEGENERATIVE HEMIBALLISMUS

1946 • 75 citations

Ataxia, Chorea, Seizures, and Dementia

1989 • 57 citations

Expansion of the (CAG)_n repeat causing Huntington's disease in 352 patients of German origin

1993 • 54 citations

The identification of neurotrophic factor as a transferrin

1983 • 53 citations

Dentatorubro‐pallidoluysian degeneration

1982 • 38 citations

Familial chorea and myoclonus epilepsy

1978 • 36 citations

Progressive myoclonus epilepsy: Dentato-rubro-pallido-luysian atrophy (DRPLA) in childhood

1991 • 27 citations

La dyssynergie cérébelleuse myoclonique (R. Hunt): Affection autonome ou variante du type dégénératif de l'épilepsie-myoclonie progressive (Unverricht-Lundborg)

1969 • 18 citations

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1972 • 13 citations

CNS Changes in DRPLA with Dementia and Personality Changes: CT, MR and SPECT Findings

1993 • 11 citations

[Hereditary dentatorubropallidoluysian atrophy--clinical variants in a family and degeneration of cerebral white matter in a proband].

1992 • 8 citations

[A clinicopathological study on familial cases of dentatorubro-pallidoluysian atrophy (DRPLA)].

1987 • 6 citations