Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies.
about
The genetic epidemiology of neurodegenerative disease.Notification and support for people exposed to the risk of Creutzfeldt-Jakob disease (CJD) (or other prion diseases) through medical treatment (iatrogenically)Notification and support for people exposed to the risk of Creutzfeldt-Jakob disease (CJD) through medical treatment (iatrogenically)Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type miceAnalysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles.Epidemiological characteristics of human prion diseasesRacial and ethnic differences in individuals with sporadic Creutzfeldt-jakob disease in the United States of AmericaGenotype-phenotype analysis in inherited prion disease with eight octapeptide repeat insertional mutation.Human transmissible spongiform encephalopathies in eleven countries: diagnostic pattern across time, 1993-2002.Genomic and post-genomic analyses of human prion diseasesRegulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains.PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.Postmortem findings in a case of variant Creutzfeldt-Jakob disease treated with intraventricular pentosan polysulfate.Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties.Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate.Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.Sex effects in mouse prion disease incubation time.Ascertainment bias causes false signal of anticipation in genetic prion diseaseVariant CJD. 18 years of research and surveillance.Age at Death of Creutzfeldt-Jakob disease in subsequent family generation carrying the E200K mutation of the prion protein gene.Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob disease.Genome-wide association study of behavioural and psychiatric features in human prion disease.Comparative Incidence of Conformational, Neurodegenerative Disorders.Rapidly progressive dementias and the treatment of human prion diseases.Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years.Phenotypic variability in human prion diseases.An In Vivo (11)C-(R)-PK11195 PET and In Vitro Pathology Study of Microglia Activation in Creutzfeldt-Jakob Disease.The prion strain phenomenon: molecular basis and unprecedented features.Diagnosis and treatment of rapidly progressive dementias.Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease.Human prion diseases: progress in clinical trials.Therapeutic approaches for prion disorders.Review. The origin of the prion agent of kuru: molecular and biological strain typing.Etiologic Framework for the Study of Neurodegenerative Disorders as Well as Vascular and Metabolic Comorbidities on the Grounds of Shared Epidemiologic and Biologic FeaturesDrivers: A Biologically Contextualized, Cross-Inferential View of the Epidemiology of Neurodegenerative Disorders.Distinct prion-like strains of amyloid beta implicated in phenotypic diversity of Alzheimer's disease.Creutzfeldt-Jakob Disease: Analysis of Four Cases.Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selectionEthics in prion disease.
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P2860
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh
2004年學術文章
@zh-hant
name
Predictors of survival in spor ...... e spongiform encephalopathies.
@en
type
label
Predictors of survival in spor ...... e spongiform encephalopathies.
@en
prefLabel
Predictors of survival in spor ...... e spongiform encephalopathies.
@en
P2093
P50
P356
P1433
P1476
Predictors of survival in spor ...... le spongiform encephalopathies
@en
P2093
Alperovitch A
Brandel JP
Delasnerie-Laupretre N
Kretzschmar HA
Ladogana A
P304
P356
10.1093/BRAIN/AWH249
P407
P577
2004-09-10T00:00:00Z