Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophy and Machado-Joseph disease.

Kumada, S; Hayashi, M; Mizuguchi, M; Nakano, I; Morimatsu, Y; Oda, M

Kumada, S; Hayashi, M; Mizuguchi, M; Nakano, I; Morimatsu, Y; Oda, M.

Affiliation

Kumada S; Department of Clinical Neuropathology, Tokyo Metropolitan Institute for Neuroscience, Fuchu-shi, Japan.

Acta Neuropathol ; 99(1): 48-54, 2000 Jan.

Article in En | MEDLINE | ID: mdl-10651027

Subject(s)

Cerebellum/pathology; Machado-Joseph Disease/pathology; Myoclonic Epilepsies, Progressive/pathology; Nerve Degeneration/pathology; ATP-Binding Cassette Transporters/metabolism; Adolescent; Adult; Aged; Amino Acid Transport System X-AG; Apoptosis; Cadaver; Calbindin 1; Calbindins; Cerebellum/metabolism; Female; Glial Fibrillary Acidic Protein/metabolism; Humans; Machado-Joseph Disease/metabolism; Male; Middle Aged; Myoclonic Epilepsies, Progressive/metabolism; Nerve Degeneration/metabolism; Proto-Oncogene Proteins c-bcl-2/metabolism; Receptor, trkB/metabolism; S100 Calcium Binding Protein G/metabolism; bcl-X Protein

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Collection: 01-internacional Database: MEDLINE Main subject: Cerebellum / Machado-Joseph Disease / Myoclonic Epilepsies, Progressive / Nerve Degeneration Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Acta Neuropathol Year: 2000 Document type: Article Affiliation country: Japan Country of publication: Germany

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