Prions (analysis) < Prions (genetics) < Prions (isolation & purification)

Facettes :

List of bibliographic references indexed by Prions (genetics)

Number of relevant bibliographic references: 8.

Ident.	Authors (with country if any)	Title
000625 (2014)	Kishore R. Kumar [Australie] ; Christine Klein	Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy".
000A96 (2013)	Annika Plate [Allemagne] ; Jens Benninghoff ; Gerald H. Jansen ; Elisabeth Wlasich ; Sabina Eigenbrod ; Alexander Drzezga ; Nathalie L. Jansen ; Hans A. Kretzschmar ; Kai Bötzel ; Dan Rujescu ; Adrian Danek	Atypical parkinsonism due to a D202N Gerstmann-Sträussler-Scheinker prion protein mutation: first in vivo diagnosed case.
000D78 (2012)	Radoslav Mat J [République tchèque] ; Gabor G. Kovacs ; Silvie Johanidesová ; Ji Keller ; Milada Mat J Ková ; Jana Nováková ; Vladimír Sigut ; Otakar Keller ; Robert Rusina	Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy.
001484 (2011)	C. Warren Olanow [États-Unis] ; K. Mcnaught [États-Unis]	Parkinson's disease, proteins, and prions: Milestones
001A28 (2010)	Kaori Nagasaka [Japon] ; Emiko Ohta [Japon] ; Takamura Nagasaka [Japon] ; Shinji Togashi [Japon] ; Michiaki Miwa [Japon] ; Yuki Nakamura [Japon] ; Kazumasa Shindo [Japon] ; Zenji Shiozawa [Japon]	Rhythmic pupillary oscillation in Creutzfeldt‐Jakob disease associated with the Glu/Lys mutation of prion protein codon 200
002201 (2009)	Jan Edler [Allemagne] ; Brit Mollenhauer [États-Unis] ; Uta Heinemann [Allemagne] ; Daniela Varges [Allemagne] ; Carola Werner [Allemagne] ; Inga Zerr [Allemagne] ; Walter J. Schulz-Schaeffer [Allemagne]	Movement disturbances in the differential diagnosis of Creutzfeldt‐Jakob disease
002806 (2008)	Edward J. Wild [Royaume-Uni] ; Ese E. Mudanohwo [Royaume-Uni] ; Mary G. Sweeney [Royaume-Uni] ; Susanne A. Schneider [Royaume-Uni] ; Jon Beck [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Martin N. Rossor [Royaume-Uni] ; Mary B. Davis [Royaume-Uni] ; Sarah J. Tabrizi [Royaume-Uni]	Huntington's disease phenocopies are clinically and genetically heterogeneous
002A30 (2008)	Claudia Cagnoli [Italie] ; Alessandro Brussino [Italie] ; Luca Sbaiz [Italie] ; Eleonora Di Gregorio [Italie] ; Cristiana Atzori [Italie] ; Paola Caroppo [Italie] ; Laura Orsi [Italie] ; Nicola Migone [Italie] ; Carlo Buffa [Italie] ; Daniele Imperiale [Italie] ; Alfredo Brusco [Italie]	A previously undiagnosed case of Gerstmann‐Sträussler‐Scheinker disease revealed by PRNP gene analysis in patients with adult‐onset ataxia

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