Citations for
1IDTF
Sporadic fatal insomnia: a case study.
Scaravilli F, Cordery RJ, Kretzschmar H, Gambetti P, Brink B, Fritz V, Temlett J, Kaplan C, Fish D, An SF, Schulz-Schaeffer WJ, Rossor MN.
Ann Neurol 48(4):665-8. 2000
2IDTF
Novel twelve-generation kindred of fatal familial insomnia from germany representing the entire spectrum of disease expression.
Harder A, Jendroska K, Kreuz F, Wirth T, Schafranka C, Karnatz N, Theallier-Janko A, Dreier J, Lohan K, Emmerich D, Cervos-Navarro J, Windl O, Kretzschmar HA, Nurnberg P, Witkowski R.
Am J Med Genet 87(4):311-6 1999
3IDTF, PRNP
Clinical features of fatal familial insomnia : phenotypic variability in relation to a polymorphism at codon 129 of the prion protein gene.
Montagna P, et al.
Brain Pathol 8 : 515-520. 1998
4IDTF, PRNP
The D178N (cis-129M) fatal familial insomnia mutation associated with diverse clinicopathologic phenotypes in an Australian kindred.
McLean CA, Storey E, Gardner RJ, Tannenberg AE, Cervenakova L, Brown P.
Neurology 49(2):552-8. 1997
5PRNP, IDTF
Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI) : codon 178 mutation and codon 129 polymorphism.
Medori R, et al.
Am J Hum Genet 53 : 822-827. 1993
6IDTF
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene.
Medori R, et al.
N Engl J Med 326 : 444-449. 1992
7IDTF
Fatal familial insomnia and familial Creutzfeldt-Jakob disease : disease phenotype determined by a DNA polymorphism.
Goldfarb LG, et al.
Science 258 : 806-808. 1992