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Diffusion-weighted MRI in familial Creutzfeldt–Jakob disease with the codon 200 mutation in the prion protein gene

✍ Scribed by Yoshio Tsuboi; Yasuhiko Baba; Katsumi Doh-ura; Akiko Imamura; Shinsuke Fujioka; Tatsuo Yamada

Book ID
119301641
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
198 KB
Volume
232
Category
Article
ISSN
0022-510X

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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