Related references
Note: Only part of the references are listed.Human Prion Diseases in the United States
Robert C. Holman et al.
PLOS ONE (2010)
Variant Creutzfeldt-Jakob Disease in France and the United Kingdom: Evidence for the Same Agent Strain
Jean-Philippe Brandel et al.
ANNALS OF NEUROLOGY (2009)
Mutations at codons 178, 200-129, and 232 contributed to the inherited prion diseases in Korean patients
Bo-Yeong Choi et al.
BMC INFECTIOUS DISEASES (2009)
Familial Creutzfeldt-Jakob Disease with a V180I Mutation: Comparative Analysis with Pathological Findings and Diffusion-Weighted Images
Kazuo Mutsukura et al.
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS (2009)
The risk of iatrogenic Creutzfeldt-Jakob disease through medical and surgical procedures
Tsuyoshi Hamaguchi et al.
NEUROPATHOLOGY (2009)
Dura mater graft-associated Creutzfeldt-Jakob disease in Japan: Clinicopathological and molecular characterization of the two distinct subtypes
Masahito Yamada et al.
NEUROPATHOLOGY (2009)
Medical Procedures and Risk for Sporadic Creutzfeldt-Jakob Disease, Japan, 1999-2008
Tsuyoshi Hamaguchi et al.
EMERGING INFECTIOUS DISEASES (2009)
PRNP mutations in a series of apparently sporadic neurodegenerative dementias in China
Liu Zheng et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2008)
Surveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007
Qi Shi et al.
BMC PUBLIC HEALTH (2008)
The M129V polymorphism of codon 129 in the prion gene (PRNP) in the Danish population
Henrik Dyrbye et al.
EUROPEAN JOURNAL OF EPIDEMIOLOGY (2008)
Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution
Yusei Shiga et al.
JOURNAL OF NEUROLOGY (2007)
Clinical features and diagnosis of dura mater graft-associated Creutzfeldt-Jakob disease
M. Noguchi-Shinohara et al.
NEUROLOGY (2007)
Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance
U. Heinemann et al.
BRAIN (2007)
Human transmissible spongiform encephalopathies in eleven countries:: diagnostic pattern across time, 1993-2002
Jesus de Pedro-Cuesta et al.
BMC PUBLIC HEALTH (2006)
Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease
S. J. Collins et al.
BRAIN (2006)
Iatrogenic Creutzfeldt-Jakob disease - The waning of an era
Paul Brown et al.
NEUROLOGY (2006)
Increased incidence of sporadic Creutzfeldt-Jakob disease in the age groups between 70 and 90 years in Belgium
B. Van Everbroeck et al.
EUROPEAN JOURNAL OF EPIDEMIOLOGY (2006)
Polymorphism of PRNP codons in the normal Icelandic population
G Georgsson et al.
ACTA NEUROLOGICA SCANDINAVICA (2006)
Clinical features and diagnosis of the MM2 cortical subtype of sporadic Creutzfeldt-Jakob disease
Anna Krasnianski et al.
ARCHIVES OF NEUROLOGY (2006)
14-3-3 protein, total tau and phosphorylated tau in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease and neurodegenerative disease in Japan
K Satoh et al.
CELLULAR AND MOLECULAR NEUROBIOLOGY (2006)
Creutzfeldt-Jakob disease risk and PRNP codon 129 polymorphism:: necessity to revalue current data
E Mitrová et al.
EUROPEAN JOURNAL OF NEUROLOGY (2005)
Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population
BH Jeong et al.
NEUROGENETICS (2005)
Genetic prion disease:: the EUROCJD experience
GG Kovács et al.
HUMAN GENETICS (2005)
Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada
A Ladogana et al.
NEUROLOGY (2005)
Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease
T Hamaguchi et al.
NEUROLOGY (2005)
Clinical features of Creutzfeldt-Jakob disease with V180I mutation
K Jin et al.
NEUROLOGY (2004)
Polymorphisms of the PRNP gene in Chinese populations and the identification of a novel insertion mutation
SL Yu et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2004)
Clinical and genetic features of human prion diseases in Catalonia:: 1993-2002
R Sanchez-Valle et al.
EUROPEAN JOURNAL OF NEUROLOGY (2004)
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies
M Pocchiari et al.
BRAIN (2004)
Creutzfeldt-Jakob disease in Ireland: Epidemiological aspects 1980-2002
G Horan et al.
EUROPEAN NEUROLOGY (2004)
Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan
T Ohkubo et al.
ANNALS OF NEUROLOGY (2003)
Mortality trend from sporadic Creutzfeldt-Jakob disease (CJD) in Italy, 1993-2000
M Puopolo et al.
JOURNAL OF CLINICAL EPIDEMIOLOGY (2003)
The normal population distribution of PRNP codon 129 polymorphism
MH Nurmi et al.
ACTA NEUROLOGICA SCANDINAVICA (2003)
Creutzfeldt-Jakob disease in Australia 1970-1999
S Collins et al.
NEUROLOGY (2002)
Incidence of Creutzfeldt-Jakob disease in Switzerland
M Glatzel et al.
LANCET (2002)