Creutzfeldt-Jakob Syndrome (classification) < Creutzfeldt-Jakob Syndrome (complications) < Creutzfeldt-Jakob Syndrome (diagnosis)

Facettes :

List of bibliographic references indexed by Creutzfeldt-Jakob Syndrome (complications)

Number of relevant bibliographic references: 8.

Ident.	Authors (with country if any)	Title
000777 (2013)	Niels Fockaert [Belgique] ; Marc Van Orshoven ; Patrick Cras ; Christine Van Broeckhoven ; Philippe Demaerel ; Wim Vandenberghe	Slowing of saccadic eye movements in sporadic Creutzfeldt-Jakob disease.
000A55 (2013)	Maria Stamelou [Grèce]	Commentary for "Slowing of saccadic eye movements in sporadic Creutzfeldt-Jakob disease".
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
001B66 (2010)	Simona Binelli [Italie] ; Pamela Agazzi [Italie] ; Laura Canafoglia [Italie] ; Vidmer Scaioli [Italie] ; Ferruccio Panzica [Italie] ; Elisa Visani [Italie] ; Giuseppe Di Fede [Italie] ; Giorgio Giaccone [Italie] ; Alberto Bizzi [Italie] ; Orso Bugiani [Italie] ; Guiliano Avanzini [Italie] ; Fabrizio Tagliavini [Italie] ; Silvana Franceschetti [Italie]	Myoclonus in Creutzfeldt‐Jakob disease: Polygraphic and video‐electroencephalography assessment of 109 patients
003134 (2006)	Keiko Ohnari [Japon] ; Kaoru Matsunaga [Japon] ; Takenori Uozumi [Japon] ; Akira Tamagawa [Japon] ; Tomoko Hashimoto [Japon] ; Sadatoshi Tsuji [Japon]	Unilateral positive–negative myoclonus in Creutzfeldt–Jakob disease
004458 (2002)	Mark A. Hellmann [Israël] ; Eldad Melamed [Israël]	Focal dystonia as the presenting sign in Creutzfeldt‐Jakob disease
004B10 (2000)	John Bowen ; Tejal Mitchell ; Ronald Pearce ; Niall Quinn [Royaume-Uni]	Chorea in new variant Creutzfeldt‐Jakob disease
006184 (1991)	Sethi [États-Unis] ; David C. Hess [États-Unis]	Creutzfeldt‐Jakob's disease presenting with ataxia and a movement disorder

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