相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。National Institute on Aging-Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease: a practical approach
Thomas J. Montine et al.
ACTA NEUROPATHOLOGICA (2012)
Human Prion Diseases in The Netherlands (1998-2009): Clinical, Genetic and Molecular Aspects
Casper Jansen et al.
PLOS ONE (2012)
Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future
Piero Parchi et al.
ACTA NEUROPATHOLOGICA (2011)
Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis
Sabina Capellari et al.
ACTA NEUROPATHOLOGICA (2011)
Variably Protease-Sensitive Prionopathy: A New Sporadic Disease of the Prion Protein
Wen-Quan Zou et al.
ANNALS OF NEUROLOGY (2010)
Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease
Piero Parchi et al.
BRAIN (2010)
Experimental Verification of a Traceback Phenomenon in Prion Infection
Atsushi Kobayashi et al.
JOURNAL OF VIROLOGY (2010)
Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties
Matthew T. Bishop et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification
Piero Parchi et al.
ACTA NEUROPATHOLOGICA (2009)
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics
Ignazio Cali et al.
BRAIN (2009)
Inter-Laboratory Assessment of PrPSc Typing in Creutzfeldt-Jakob Disease: A Western Blot Study within the NeuroPrion Consortium
Piero Parchi et al.
BRAIN PATHOLOGY (2009)
Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients
Atsushi Kobayashi et al.
ACTA NEUROPATHOLOGICA (2008)
Characterization of Truncated Forms of Abnormal Prion Protein in Creutzfeldt-Jakob Disease
Silvio Notari et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Mechanisms of disease - Insights into prion strains and neurotoxicity
Adriano Aguzzi et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2007)
Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles
Romolo Nonno et al.
PLOS PATHOGENS (2006)
Effects of different experimental conditions on the PrPSc core generated by protease digestion - Implications for strain typing and molecular classification of CJD
S Notari et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002
MW Head et al.
ANNALS OF NEUROLOGY (2004)
Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene
C Korth et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Hereditary prion protein amyloidoses
B Ghetti et al.
CLINICS IN LABORATORY MEDICINE (2003)
Sporadic and familial CJD: classification and characterisation
P Gambetti et al.
BRITISH MEDICAL BULLETIN (2003)
Strain characterization of natural sheep scrapie and comparison with BSE
ME Bruce et al.
JOURNAL OF GENERAL VIROLOGY (2002)
Pathological diagnosis of variant Creutzfeldt-Jakob disease
JW Ironside et al.
APMIS (2002)
Genetic influence on the structural variations of the abnormal prion protein
P Parchi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
分享论文
