Fatal Familial Insomnia

Known as: insomnia fatal familial, Fatals, Insomnia Familial, Insomnias, Fatal Familial 
A very rare autosomal dominant inherited sleep disorder caused by a mutation in the gene responsible for the prion protein. It affects individuals… (More)
National Institutes of Health

Papers overview

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Review
2017
Review
2017
Flexible/adaptive acoustic modems that are reprogrammable/reconfigurable at all layers of the communication stack, either by a… (More)
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Highly Cited
2011
Highly Cited
2011
Several families have been reported with autosomal-dominant frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS… (More)
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Review
2003
Review
2003
Familial fatal insomnia (FFI)--a hereditary prion disease caused by a mutation at codon 178 of the prion-protein (PrP) gene (PRNP… (More)
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1999
1999
We present clinical, pathological and molecular features of the first Austrian family with fatal familial insomnia. Detailed… (More)
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Review
1998
Review
1998
Fatal familial insomnia (FFI) is linked to a mutation at codon 178 of the prion protein gene, coupled with the methionine codon… (More)
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Highly Cited
1995
Highly Cited
1995
ORIGINALLY described by Lugaresi et al. in 1986 (ref. 1), fatal familial insomnia (FFI) is a rare inherited neurological disease… (More)
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Highly Cited
1994
Highly Cited
1994
Fatal familial insomnia and a subtype of Creutzfeldt-Jakob disease, two clinically and pathologically distinct diseases, are… (More)
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Highly Cited
1992
Highly Cited
1992
Fatal familial insomnia (FFI) and a subtype of familial Creutzfeldt-Jakob disease (CJD), two clinically and pathologically… (More)
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Highly Cited
1992
Highly Cited
1992
BACKGROUND We previously described two members of a family affected by an apparently genetically determined fatal disease… (More)
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Highly Cited
1991
Highly Cited
1991
A LOCUS segregating with familial Alzheimer's disease (AD) has been mapped to chromosome 21 (ref. 1), close to the amyloid… (More)
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