Human prion disease

Keywords

Fatal familial insomnia, Magnetic resonance imaging, Disease, Cerebrospinal fluid, Medicine

References

• Validation of 14-3-3 Protein as a Marker in Sporadic Creutzfeldt-Jakob Disease DiagnosticMatthias Schmitz, Elisabeth Ebert, Katharina Stoeck — 2016
• The Levels of Tau Isoforms Containing Exon-2 and Exon-10 Segments Increased in the Cerebrospinal Fluids of the Patients with Sporadic Creutzfeldt-Jakob DiseaseCao Chen, Wei Zhou, Yan Lv — 2015
• The clinical neurology and epidemiology of Creutzfeldt-Jakob disease, with special reference to iatrogenic cases.Paul Brown — 1988
• Descriptive Epidemiology of Prion Disease in Japan: 1999–2012Yosikazu Nakamaura, Ryusuke Ae, Ichiro Takumi — 2014
• Typing prion isoformsPiero Parchi, Sabina Capellari, Shu G. Chen — 1997
• Periodic synchronous discharge and myoclonus in Creutzfeldt‐Jakob disease: Diagnostic application of jerk‐locked averaging methodHiroshi Shibasaki, Satoru Motomura, Yoriaki Yamashita — 1981
• Tau protein and 14-3-3 protein in the differential diagnosis of Creutzfeldt–Jakob diseaseMarkus Otto, Jens Wiltfang, Lukas Cepek — 2002
• Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation.Kiyotoshi Kaneko, Laurence Zulianello, Michael Scott — 1997
• Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathyGábor G. Kovács, Jérémie Seguin, Isabelle Quadrio — 2010
• Genetic prion disease: the EUROCJD experienceGábor G. Kovács, Maria Puopolo, Anna Ladogana — 2005
• Molecular analysis of prion strain variation and the aetiology of 'new variant' CJDJohn Collinge, Katie Sidle, Julie Meads — 1996
• Characterization of Truncated Forms of Abnormal Prion Protein in Creutzfeldt-Jakob Disease*Silvio Notari, Rosaria Strammiello, Sabina Capellari — 2008
• Iatrogenic Creutzfeldt-Jakob disease via surgical instruments.Jonathan G. Thomas, Carol Chenoweth, Stephen E. Sullivan — 2013
• Phospho-tau/total tau ratio in cerebrospinal fluid discriminates Creutzfeldt–Jakob disease from other dementiasMarkus J. Riemenschneider, Stefan Wagenpfeil, Hugo Vanderstichele — 2003
• Genetic influence on the structural variations of the abnormal prion protein.Piero Parchi, Wen‐Quan Zou, Wen Wang — 2000
• Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjectsPiero Parchi, Armin Giese, Sabina Capellari — 1999
• Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosis.Geoffrey S. Young, Michael D. Geschwind, Nancy J. Fischbein — 2005
• High sensitivity of an ELISA kit for detection of the gamma-isoform of 14-3-3 proteins: usefulness in laboratory diagnosis of human prion diseaseYuki Matsui, Katsuya Satoh, Toshiaki Miyazaki — 2011
• Sporadic and familial CJD: classification and characterisation.Pierluigi Gambetti, Qingzhong Kong, Wen‐Quan Zou — 2003
• Protective prion protein polymorphisms against sporadic Creutzfeldt-Jakob disease.S. SHIBUYA, Jiro Higuchi, R-W Shin — 1998

Cited by

• Research in the Field of Drug Design and DevelopmentGrażyna Biała, Ewa Kędzierska, Marta Kruk-Słomka — 2023
• Genetic characterization of the prion protein gene in camels (Camelus) with comments on the evolutionary history of prion disease in CetartiodactylaEmily A. Wright, Madison B. Reddock, E. Roberts — 2024

Related papers

• Pathological Prion Protein in the Tongues of Sheep Infected with Naturally Occurring ScrapieCristina Casalone, Cristiano Corona, Maria Ines Crescio — 2005
• Human transmissible spongiform encephalopathies: historic view.David M. Asher, Luisa Gregori — 2018
• Historical overview of prion diseases: a view from afar.Paweł P. Liberski — 2012
• Molecular structure, biology, and genetics of prions.Stanley B. Prusiner — 1988
• Atypical prion diseases in humans and animals.Michael A. Tranulis, Sylvie L. Benestad, Thierry Baron — 2011
• Prion-protein-related diseases of animals and manJames Hope, Mark P. Dagleish — 2011