Related references
Note: Only part of the references are listed.Divergent clinical and neuropathological phenotype in a Gerstmann-Straussler-Scheinker P102L family
S. N. Popova et al.
ACTA NEUROLOGICA SCANDINAVICA (2012)
Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis
Sabina Capellari et al.
ACTA NEUROPATHOLOGICA (2011)
Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion
Ryuichiro Atarashi et al.
NATURE MEDICINE (2011)
Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt-Jakob disease
Katsuya Satoh et al.
LABORATORY INVESTIGATION (2010)
Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies
Anna Ladogana et al.
JOURNAL OF NEUROLOGY (2009)
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series
T. E. F. Webb et al.
BRAIN (2008)
Share Paper
