Fatal Familial Insomnia

Fatal familial insomnia is a familial prion disease linked to a mutation of the prion protein gene. Here is the latest research on this rare genetic degenerative brain disorder.

October 24, 2021
Open Access

Defining the Prion Type of Fatal Familial Insomnia.

Wiebke Jürgens-WemheuerWalter Schulz-Schaeffer
October 21, 2021

Clinical profile of fatal familial insomnia: phenotypic variation in 129 polymorphisms and geographical regions.

Journal of Neurology, Neurosurgery, and Psychiatry
Jing ZhangLi-Yong Wu
September 6, 2021
Case Report

Genetic Creutzfeldt-Jakob disease shows fatal family insomnia phenotype.

Bin ChenYong You
September 1, 2021
Case Report

Sporadic Creutzfeldt-Jakob Disease Appears to Be Sporadic Fatal Insomnia: A Case Report and Review of the Literature.

Nature and Science of Sleep
Qingqing SunLi Cui
July 30, 2021
Open Access

Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.

Acta Neuropathologica
Simone BaiardiPiero Parchi
July 6, 2021
Open Access

Diagnostic and prognostic performance of CSF α-synuclein in prion disease in the context of rapidly progressive dementia.

Alzheimer's & Dementia : Diagnosis, Assessment & Disease Monitoring
Andrea MastrangeloPiero Parchi
July 3, 2021
Open Access

MicroRNAs in Prion Diseases-From Molecular Mechanisms to Insights in Translational Medicine.

Danyel Fernandes ContilianiTiago Campos Pereira
June 23, 2021
Case Report

Fatal insomnia: the elusive prion disease.

BMJ Case Reports
Dharmini PatelAdam Zeman
June 21, 2021

[Prion diseases or transmissible spongiform encephalopathies].

La Revue de médecine interne
J-P Brandel
June 9, 2021

Mediodorsal thalamus lesion increases paradoxical sleep in rats.

Sleep Science
S N SrijiHruda Nanda Mallick
May 18, 2021
Comment / Editorial
Open Access

JNO Literature Commentary.

Journal of Neuro-ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
April 21, 2021
Open Access

TREM2 expression in the brain and biological fluids in prion diseases.

Acta Neuropathologica
Daniela Diaz-LucenaFranc Llorens
March 9, 2021
Open Access

Genetic prion disease: D178N with 129MV disease modifying polymorphism-a clinical phenotype.

BMJ Neurology Open
Tracie Huey-Lin TanMastura Monif
March 5, 2021
Open Access

Activation of Src family kinase ameliorates secretory trafficking in mutant prion protein cells.

The Journal of Biological Chemistry
Elena RestelliRoberto Chiesa
February 10, 2021

Clinical manifestations and polysomnography-based analysis in nine cases of probable sporadic Creutzfeldt-Jakob disease.

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Yanyuan DaiLi Cui
February 4, 2021
Comment / Editorial
Open Access

Thirty years of fatal familial insomnia and autonomic research: celebrating the past, embracing the future.

Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
Pietro Cortelli

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