Fatal Familial Insomnia Latest Advances

Find the Latest Research About Fatal Familial Insomnia

Last Updated: 09/26/2026

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Found 312 publications

A sleep that never comes: Prions and their role in fatal familial insomnia - a literature review.

A sleep that never comes: Prions and their role in fatal familial insomnia - a literature review.

Journal: Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego

Published: July 11, 2026

Transmission Ratio Distortion in Genetic Prion Diseases: Clarifying Methodological Considerations.

Transmission Ratio Distortion in Genetic Prion Diseases: Clarifying Methodological Considerations.

Journal: European journal of neurology

Published: January 28, 2026

Letter to the Editor Regarding Kortazar-Zubizarreta et al. 'The Risk of Transmission of Genetic Prion Diseases Is Greater Than 50%'.

Letter to the Editor Regarding Kortazar-Zubizarreta et al. 'The Risk of Transmission of Genetic Prion Diseases Is Greater Than 50%'.

Journal: European journal of neurology

Published: January 18, 2026

Prion protein (PrP) profiles in blood and CSF: insights into pre-symptomatic and symptomatic prion disease.

Prion protein (PrP) profiles in blood and CSF: insights into pre-symptomatic and symptomatic prion disease.

Journal: Brain communications

Published: January 15, 2026

Infecting human brain organoids with FFI or sCJD preserves prion traits regardless of host genotype.

Infecting human brain organoids with FFI or sCJD preserves prion traits regardless of host genotype.

Journal: NPJ dementia

Published: October 06, 2025

Advancing prion diagnostics: full-length human E200K RT-QuIC substrate facilitates prion detection in tear fluid and improves sensitivity in cerebrospinal fluid.

Advancing prion diagnostics: full-length human E200K RT-QuIC substrate facilitates prion detection in tear fluid and improves sensitivity in cerebrospinal fluid.

Journal: Acta neuropathologica communications

Published: July 25, 2025

D178N prion protein mutation endows RML prions with new strain properties that do not mimic human genetic prion diseases.

D178N prion protein mutation endows RML prions with new strain properties that do not mimic human genetic prion diseases.

Journal: Acta neuropathologica

Published: July 22, 2025

Pedigree analysis and genetic inheritance of fatal familial insomnia (FFI) in a Portuguese multigenerational family.

Pedigree analysis and genetic inheritance of fatal familial insomnia (FFI) in a Portuguese multigenerational family.

Journal: Journal of neurology

Published: June 23, 2025

Unusual occurrence of temporo-spatial cluster of human prion disease in northern part of central Slovakia.

Unusual occurrence of temporo-spatial cluster of human prion disease in northern part of central Slovakia.

Journal: Central European journal of public health

Published: May 31, 2025

Parkinsonism in Gerstmann-Sträussler-Scheinker disease: A case report.

Parkinsonism in Gerstmann-Sträussler-Scheinker disease: A case report.

Journal: eNeurologicalSci

Published: May 16, 2025

Follow-up multimodal changes on PET/MRI in fatal familial insomnia patient: a case report.

Follow-up multimodal changes on PET/MRI in fatal familial insomnia patient: a case report.

Journal: BMC neurology

Published: January 08, 2025

Sporadic Creutzfeldt-Jakob Disease: A Case Report and Literature Review.

Sporadic Creutzfeldt-Jakob Disease: A Case Report and Literature Review.

Journal: Cureus

Published: December 29, 2024

Showing 1-12 of 312

Last Updated: 09/26/2026