Familial Creutzfeldt–Jakob disease homozygous to the E200K mutation: clinical characteristics and disease course

Creutzfeldt-Jakob Disease: Focus among Libyan Jews in Israel

Esther Kahana, Milton Alter, J. Braham et al. · Science · 1974 · 153 citations

Veterinary Medicine, Genetics, Disease Surveillance +6

Complete Penetrance of Creutzfeldt-Jakob Disease in Libyan Jews Carrying the E200K Mutation in the Prion Protein Gene

Serena Spudich, James A. Mastrianni, Margaret Wrensch et al. · Molecular Medicine · 1995 · 94 citations · Full text

Veterinary Medicine, Genetics, Molecular Genetics +16

The risk of developing Creutzfeldt‐Jakob disease in subjects with the PRNP gene codon 200 point mutation

Joab Chapman, Joshua Ben-Israel, Yochanan Goldhammer et al. · Neurology · 1994 · 90 citations

Life Sciences, Genetics, Molecular Genetics +17

Clinical course in young patients with sporadic Creutzfeldt–Jakob disease

Constanze Boesenberg, Walter Schulz‐Schaeffer, Kai Kallenberg et al. · Annals of Neurology · 2005 · 59 citations

Medicine, Neurology, Psychiatry +16

Clinical manifestations of homozygote allele carriers in Huntington disease

Esther Cubo, Saül Martínez‐Horta, Asunción Martínez Descalls et al. · Neurology · 2019 · 55 citations · Full text

Life Sciences, Genetics, Neurology +17