Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype

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

1993 • 1,596 citations

Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)

1989 • 931 citations

The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology

1994 • 369 citations

The gene for Machado–Joseph disease maps to human chromosome 14q

1993 • 337 citations

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11

1994 • 317 citations

Mapping of mutation causing Friedreich's ataxia to human chromosome 9

1988 • 307 citations

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1

1993 • 278 citations

THE OLIVOPONTOCEREBELLAR ATROPHIES

1970 • 267 citations

Epidemiology and clinical aspects of Machado-Joseph disease.

1993 • 207 citations

Dominantly inherited olivopontocerebellar atrophy from eastern Cuba

1989 • 180 citations

HEREDITARY ATAXIA

1950 • 172 citations

Autosomal dominant cerebellar ataxia

1990 • 167 citations

Neurofibrillary axonal swellings and amyotrophic lateral sclerosis

1984 • 164 citations

Olivopontocerebellar Atrophy

2016 • 158 citations

The olivopontocerebellar atrophies.

1984 • 151 citations

Cognitive deficits in olivopontocerebellar atrophy: Implications for the cholinergic hypothesis of Alzheimer's dementia

1988 • 137 citations

Autosomal dominant cerebellar ataxia with retinal degeneration

1994 • 131 citations

Spinocerebellar degenerations in Japan: a nationwide epidemiological and clinical study

1994 • 106 citations

On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family

1994 • 102 citations

Hereditary ataxia: a pathologic study of five cases of common ancestry.

1951 • 55 citations

The neuropathology of olivopontocerebellar atrophy.

1984 • 54 citations

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.

1994 • 53 citations

Autosomal‐dominant dentatorubropallidoluysian atrophy in the United Kingdom

1994 • 45 citations

Cerebral cortical pathology of sporadic olivopontocerebellar atrophy

1993 • 43 citations

Selective delayed alternation deficits in dominantly inherited olivopontocerebellar atrophy

1991 • 28 citations

Oligodendroglial and neuronal inclusions in multiple system atrophy

1993 • 17 citations

Machado‐Joseph Disease in Japan: Clinicopathological Study of 6 Autopsy Cases with Special Reference to the Clinicopathological Correlation to Cerebellar Ataxia and Lower Motor Neuron Signs

1994 • 17 citations

[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)].

1991 • 6 citations

[Neuropathological study of autosomal dominant ataxia linked to loci on chromosome 6p (SCA 1)].

1993 • 4 citations

[Linkage study of hereditary spinocerebellar ataxia, and probable correlation for the loci to the disease phenotypes].

1993 • 4 citations

An Autopsied Case of Dentatorubropallidoluysian Atrophy with Atypical Pathological Features

1992 • 2 citations

[An autopsied case of type 2 Machado-Joseph's disease or spino-pontine degeneration].

1993 • 1 citations