Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real-Time QUIC Assay

Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L family

(2012) S. N. Popova et al.   ACTA NEUROLOGICA SCANDINAVICA

Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion

(2011) Ryuichiro Atarashi et al.   NATURE MEDICINE

Genetic Creutzfeldt–Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis

(2010) Sabina Capellari et al.   ACTA NEUROPATHOLOGICA

Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt–Jakob disease

(2010) Katsuya Satoh et al.   LABORATORY INVESTIGATION

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies

(2009) Anna Ladogana et al.   JOURNAL OF NEUROLOGY

Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series

(2008) T. E. F. Webb et al.   BRAIN