Creutzfeldt-Jakob Disease

Creutzfeldt-Jakob Disease is a fatal neurodegenerative disease caused due to aggregation and accumulation of misfolded prion proteins. Here are the latest discoveries pertaining to this disease.

May 22, 2020

Refractory status epilepticus in genetic Creutzfeldt-Jakob disease with E200K mutation

Neurología : publicación oficial de la Sociedad Española de Neurología
A Gómez RoldósJ R Pérez Sánchez
June 24, 2020

Diagnosis of Prion Diseases by RT-QuIC Results in Improved Surveillance

Neurology
Daniel D RhoadsBrian S Appleby
June 5, 2020
Open Access

Molecular Dynamics Studies of Dog Prion Protein Wild-type and Its D159N Mutant

Journal of Biomolecular Structure & Dynamics
Jiapu Zhang
June 23, 2020
Review

Genetic risk factors for Creutzfeldt-Jakob disease

Neurobiology of Disease
Emma Jones, Simon Mead
May 21, 2020

18F-FDG PET/CT in Sporadic Creutzfeldt-Jakob Disease

Clinical Nuclear Medicine
Ghali ZiziDavid Morland
June 25, 2020

Creutzfeldt-Jakob Disease: A single center experience and systemic analysis of cases in Turkey

Ideggyógyászati szemle
Ferda Ilgen UsluGulsen Babacan Yildiz
June 17, 2020

Transmission of CJD from nasal brushings but not spinal fluid or RT-QuIC product

Annals of Clinical and Translational Neurology
Gregory J RaymondByron Caughey
May 5, 2020

The Braak hypothesis in prion disease with a focus on Creutzfeldt-Jakob disease

Neuropathology : Official Journal of the Japanese Society of Neuropathology
Yasushi Iwasaki
May 21, 2020
Case Report
Open Access

Functional Magnetic Resonance Imaging in the Final Stage of Creutzfeldt-Jakob Disease

Diagnostics
Stefan M GolaszewskiEugen Trinka
June 21, 2020

Editorial for JCD - July, 2020

Journal of Cosmetic Dermatology
Michael H Gold

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