Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution-Reference-Cited by-同舟云学术

Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution

Published:2007-11 Issue:11 Volume:254 Page:1509-1517
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Shiga* Y.,Satoh K.,Kitamoto* T.,Kanno S.,Nakashima I.,Sato S.,Fujihara K.,Takata H.,Nobukuni K.,Kuroda* S.,Takano H.,Umeda Y.,Konno H.,Nagasato K.,Satoh A.,Matsuda Y.,Hidaka M.,Takahashi H.,Sano Y.,Kim K.,Konishi T.,Doh-ura K.,Sato* T.,Sasaki K.,Nakamura* Y.,Yamada* M.,Mizusawa* H.,Itoyama Y.

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-007-0540-9.pdf

Reference33 articles.

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2. Kovács GG, Trabattoni G, Heinfellner JA, Ironside JW, Knight RSG, Budka H (2002) Mutations of the prion protein gene: Phenotypic spectrum. J Neurol 249:1567–1582

3. Parchi P, Giese A, Capellari S, et al. (1999) Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 46:224–233

4. Kitamoto T, Ohta M, Doh-ura K, Hitoshi S, Terao Y, Tateishi J (1993) Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann- Sträussler Syndrome. Biochem Biophys Res Commun 191:709–714

5. Shimizu T, Tanaka K, Tanahashi N, Fukuuchi Y, Kitamoto T (1994) Creutzfeldt-Jakob disease with a point mutation at codon 232 of prion protein – A case report. Clin Neurol 34:590–592

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