Kumada, S <br/><br/>
Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophy and Machado-Joseph disease.  [electronic resource] 

 -  Acta neuropathologica  Jan 2000 
 - 48-54 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0001-6322 
<br/><br/><label>Standard No.: </label>10.1007/pl00007405  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATP-Binding Cassette Transporters--metabolism<br/>Adolescent<br/>Adult<br/>Aged<br/>Amino Acid Transport System X-AG<br/>Apoptosis<br/>Cadaver<br/>Calbindin 1<br/>Calbindins<br/>Cerebellum--metabolism<br/>Female<br/>Glial Fibrillary Acidic Protein--metabolism<br/>Humans<br/>Machado-Joseph Disease--metabolism<br/>Male<br/>Middle Aged<br/>Myoclonic Epilepsies, Progressive--metabolism<br/>Nerve Degeneration--metabolism<br/>Proto-Oncogene Proteins c-bcl-2--metabolism<br/>Receptor, trkB--metabolism<br/>S100 Calcium Binding Protein G--metabolism<br/>bcl-X Protein