✦ LIBER ✦

An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion protein

✍ Scribed by Tetsuo Hama; Yasushi Iwasaki; Hisayoshi Niwa; Mari Yoshida; Yoshio Hashizume; Tetsuyuki Kitamoto; Nobuyuki Murakami; Gen Sobue

Book ID: 108958149
Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 654 KB
Volume: 29
Category: Article
ISSN: 0919-6544
DOI: 10.1111/j.1440-1789.2009.01016.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutation in the prion protein gene at co

Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study

✍ Mohammad Zahirul Hoque; Tetsuyuki Kitamoto; Hisako Furukawa; Tamaki Muramoto; Ju 📂 Article 📅 1996 🏛 Springer-Verlag 🌐 English ⚖ 351 KB

Creutzfeldt-Jakob disease in a patient w

Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment

✍ Sigrun Roeber; Bjarne Krebs; Manuela Neumann; Otto Windl; Inga Zerr; Eva-Maria G 📂 Article 📅 2005 🏛 Springer-Verlag 🌐 English ⚖ 362 KB

Autopsy case of Creutzfeldt–Jakob diseas

Autopsy case of Creutzfeldt–Jakob disease with Met/Val heterozygosity at codon 129 and type 1 protease-resistant prion protein presenting some florid-type plaques and many Kuru plaques in the cerebellum

✍ Yoko Kawauchi; Toshiaki Kamitani; Saburo Yagishita; Tetsuyuki Kitamoto; Hitaru K 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 278 KB

Rhythmic pupillary oscillation in Creutz

Rhythmic pupillary oscillation in Creutzfeldt-Jakob disease associated with the Glu/Lys mutation of prion protein codon 200

✍ Kaori Nagasaka; Emiko Ohta; Takamura Nagasaka; Shinji Togashi; Michiaki Miwa; Yu 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 438 KB

## Abstract We report two Creutzfeldt‐Jakob disease (CJD) patients with rhythmic pupillary and palpebral oscillation who had a mutation of prion protein codon 200 that resulted in the substitution of lysine for glutamate (Glu/Lys). Alternating dilation and constriction of the pupils combined with e

Polymorphisms at codons 56 and 174 of th

Polymorphisms at codons 56 and 174 of the prion-like protein gene (PRND) are not associated with sporadic Creutzfeldt-Jakob disease

✍ Byung-Hoon Jeong; Nam-Ho Kim; Jae-Il Kim; Richard I. Carp; Yong-Sun Kim 📂 Article 📅 2005 🏛 Nature Publishing Group 🌐 English ⚖ 198 KB

An autopsy case of Creutzfeldt-Jakob dis

An autopsy case of Creutzfeldt-Jakob disease with a V180I mutation of the PrP gene and Alzheimer-type pathology

✍ Hidenori Yoshida; Seishi Terada; Hideki Ishizu; Kenji Ikeda; Toshiyuki Hayabara; 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 377 KB