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Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews

scientific article published on July 1997

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Europe PubMed Central

10 September 2017

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Europe PubMed Central

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Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews (English)

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Europe PubMed Central

10 September 2017

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Prusiner SB

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Europe PubMed Central

10 September 2017

Meiner Z

1

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Europe PubMed Central

PubMed ID

9279329

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10 September 2017

Gabizon R

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Europe PubMed Central

PubMed ID

9279329

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10 September 2017

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English

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1 July 1997

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Europe PubMed Central

10 September 2017

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Europe PubMed Central

10 September 2017

76

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Europe PubMed Central

10 September 2017

227-237

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Europe PubMed Central

10 September 2017

4

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Europe PubMed Central

10 September 2017

Brain SPECT imaging with Tc-99m HM-PAO in Creutzfeld-Jakob disease

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Subacute spongiform encephalopathy and its relation to Jakob-Creutzfeldt disease: report on six cases

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Transmissible spongiform encephalopathy (Creutzfeldt-Jakob disease). Atypical clinical and pathological findings.

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The apolipoprotein E alleles as major susceptibility factors for Creutzfeldt-Jakob disease. The French Research Group on Epidemiology of Human Spongiform Encephalopathies.

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Separation and properties of cellular and scrapie prion proteins

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Creutzfeldt-Jakob disease in Benghazi, Libya

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Creutzfeldt-Jakob disease prion proteins in human brains

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Neurologic genetic diseases of Jewish people

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Fatal familial insomnia: clinical and pathologic study of five new cases

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Neuronal degeneration and neurofilament accumulation in the trigeminal ganglia in Creutzfeldt-Jakob disease

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Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.

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Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease

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NMR structure of the mouse prion protein domain PrP(121-231)

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Creutzfeldt-Jakob disease: Familial clustering among Libyan-born Israelis

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Proposed three-dimensional structure for the cellular prion protein

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Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation

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Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin

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Analysis of the prion protein gene in thalamic dementia

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Scrapie in mice deficient in apolipoprotein E or glial fibrillary acidic protein

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

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The Libyan Creutzfeldt-Jakob disease focus in Israel: an epidemiologic evaluation

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Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

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Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.

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Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.

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Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

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A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann‐Sträussler syndrome

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Strategies for multilocus linkage analysis in humans

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Creutzfeldt-Jakob Disease: Hypothesis for High Incidence in Libyan Jews in Israel

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Molecular biology and genetics of neurodegenerative diseases caused by prions

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Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases.

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Acute ascending polyradiculoneuritis in a case of Creutzfeldt-Jakob disease

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Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Straussler-Scheinker syndrome

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Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

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Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease

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Monitoring treatment with aminoglycoside antibiotics

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Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

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Do Creutzfeldt-Jakob disease patients of Jewish Libyan origin have unique clinical features?

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Epidemiology of Creutzfeldt-Jakob disease in the United States, 1979-1990: analysis of national mortality data

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Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein

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Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

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11 October 2022

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Molecular biology and genetics of prion diseases

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Demyelinating peripheral neuropathy in Creutzfeldt-Jakob disease

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Genetics and biochemistry of Creutzfeldt-Jakob disease in Libyan Jews

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Genetic and Environmental Factors Determining the Development of Creutzfeldt-Jakob Disease in Libyan Jews

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Creutzfeldt-Jakob Disease: Focus among Libyan Jews in Israel

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Pruritus in Creutzfeldt-Jakob disease

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Differential Metabolic Effects of Adenovirus-mediated Glucokinase and Hexokinase I Overexpression in Rat Primary Hepatocytes

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The risk of developing Creutzfeldt-Jakob disease in subjects with the PRNP gene codon 200 point mutation

1 reference

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A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin

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High incidence of Creutzfeldt-Jakob disease in North African immigrants to France

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Presence of prion protein in peripheral tissues of Libyan Jews with Creutzfeldt-Jakob disease

1 reference

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Immunoblotting of Creutzfeldt-Jakob disease prion proteins: host species-specific epitopes

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Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins

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Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein gene.

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The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease.

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Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families

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Diagnosis of Creutzfeldt-Jakob disease by Western blot identification of marker protein in human brain tissue.

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Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

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11 October 2022

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Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20.

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Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.

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Computed tomography findings in 15 cases of Creutzfeldt-Jakob disease with histological verification

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Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

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Aminoacid polymorphism in human prion protein and age at death in inherited prion disease

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Structural clues to prion replication

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Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

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Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

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11 October 2022

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Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

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Novel proteinaceous infectious particles cause scrapie

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Identifiers

DOI

10.1097/00005792-199707000-00001

1 reference

stated in

Europe PubMed Central

10 September 2017

1 reference

Europe PubMed Central

PubMed ID

9279329

retrieved

10 September 2017

(Q39241829)

Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews

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