{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,21]],"date-time":"2025-09-21T17:51:38Z","timestamp":1758477098363},"reference-count":28,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2006,7,20]],"date-time":"2006-07-20T00:00:00Z","timestamp":1153353600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neuropathology"],"published-print":{"date-parts":[[2006,8]]},"abstract":"<jats:p>Autosomal dominant cerebellar ataxia (ADCA) is a group of heterogeneous conditions. More than 20 genes or gene loci have been identified that are responsible for ADCA. Although expansions of the trinucleotide (CAG) repeat that encode polyglutamine are known to cause some forms of ADCA, growing knowledge about the genetic basis of ADCA indicates that many subtypes of ADCA are caused by mutations other than the CAG repeat\/polyglutamine expansion. In this paper, we review ADCA caused by mutations other than polyglutamine expansions (i.e. \u201cnon\u2010polyglutamine diseases\u201d). We also describe the neuropathology of chromosome 16q22.1\u2010linked ADCA, which appears to be the most common non\u2010polyglutamine disease in Japan. What we find to be characteristic on the chromosome 16q22.1\u2010linked ADCA brain is the presence of atrophic Purkinje cells surrounded by the formation of amorphous material, the latter composed of the Purkinje cell dendrites stemming from the cell bodies, the presynaptic terminals innervated by certain neurons, and the astroglial processes. Such neuropathological findings seem to be unique for this disease.<\/jats:p>","DOI":"10.1111\/j.1440-1789.2006.00719.x","type":"journal-article","created":{"date-parts":[[2006,7,20]],"date-time":"2006-07-20T09:22:17Z","timestamp":1153387337000},"page":"352-360","source":"Crossref","is-referenced-by-count":11,"title":["On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1\u2010linked ADCA"],"prefix":"10.1111","volume":"26","author":[{"given":"Kinya","family":"Ishikawa","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hidehiro","family":"Mizusawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2006,7,20]]},"reference":[{"key":"e_1_2_5_2_2","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/105.1.1"},{"key":"e_1_2_5_3_2","doi-asserted-by":"publisher","DOI":"10.1086\/514867"},{"key":"e_1_2_5_4_2","unstructured":"GrahamDI LantosPL eds.Greenfield\u2019s Neuropathology 7th edn Vol.2. 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