Analysis of a large case series of fatal familial insomnia to determine tests with the highest diagnostic value

Author:

Kortazar-Zubizarreta Izaro,Eraña Hasier,Pereda Arrate,Charco Jorge M,Manero-Azua Africa,Ruiz-Onandi Rebeca,Aguirre Urko,Gonzalez-Chinchon Gonzalo,Prieto-Tedejo R,Somme J H,Perez Arantza Onaindia,Garcia-Moncó J C,Matute A,Uterga J M,Antigüedad A R,Losada J M,Velasco-Palacios L,Pinedo-Brochado A,Escalza I,González-Pinto T,López de Munain A,Moreno F,Zarranz Juan José,Pozo Nagore Siles,Jimenez Karol,Piñeiro Patricia,Perez de Nanclares Guiomar,Castilla Joaquín,

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine

Reference48 articles.

1. Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei;Lugaresi;N Engl J Med,1986

2. Expert consensus on clinical diagnostic criteria for fatal familial insomnia;Wu;Chin Med J (Engl),2018

3. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Disease phenotype determined by a DNA polymorphism;Goldfarb;Science,1992

4. Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): Codon 178 mutation and codon 129 polymorphism;Medori;Am J Hum Genet,1993

5. Fatal familial insomnia and familial Creutzfeldt Jakob disease: Different prion proteins determined by a DNA polymorphism;Monari;Proc Natl Acad Sci USA,1994

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