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Article

Two Norwegian sisters with late onset Creutzfeldt-Jakob disease caused by the E200K mutation.

Journal of neurology - 1 Feb 2007

Farbu Elisabeth, Tysnes Ole-Bjørn, Mørk Sverre, Krossnes Bård K, Bindoff Laurence A

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PMID: 17334659
DOI: 10.1007/s00415-006-0363-0

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Two Norwegian sisters with late onset Creutzfeldt-Jakob disease caused by the E200K mutation.PMID 17334659Read ↗

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The first case of variant Creutzfeldt-Jakob disease in The Netherlands.Semantic proximity Read ↗

Familial Creutzfeldt-Jakob disease homozygous to the E200K mutation: clinical characteristics and disease course.Semantic proximity Read ↗

Sporadic Creutzfeldt-Jakob disease: discrete subtypes or a spectrum of disease?Semantic proximity Read ↗

Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families.Semantic proximity Read ↗

Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation.Semantic proximity Read ↗

A Creutzfeldt-Jakob disease patient with V180I mutation survived for 16.5 years after diagnosis.Semantic proximity Read ↗

Creutzfeldt-Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNP.Semantic proximity Read ↗

Variant Creutzfeldt-Jakob disease.Semantic proximity Read ↗

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