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Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia.
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scholarly article
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Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
main subject
insomnia
0 references
Creutzfeldt-Jakob disease
1 reference
based on heuristic
inferred from title
author
Piero Parchi
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
Shu Chen
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
Pierluigi Gambetti
series ordinal
1
object named as
Pierluigi Gambetti
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
publication date
1 March 2003
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
published in
Clinics in laboratory medicine
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
volume
23
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
page(s)
43-64
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
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Creutzfeldt-Jakob Disease: Focus among Libyan Jews in Israel
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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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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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Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families
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Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.
1 reference
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High incidence of Creutzfeldt-Jakob disease in rural Calabria, Italy
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Genetic and Environmental Factors Determining the Development of Creutzfeldt-Jakob Disease in Libyan Jews
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Crossref
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7 January 2021
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A prion protein variant in a family with the telencephalic form of Gerstmann-Straussler-Scheinker syndrome
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7 January 2021
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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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7 January 2021
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Strategies for multilocus linkage analysis in humans
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7 January 2021
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Neurologic genetic diseases of Jewish people
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7 January 2021
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Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy
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7 January 2021
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Inherited prion disease (PrP lysine 200) in Britain: two case reports
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Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.
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7 January 2021
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Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
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7 January 2021
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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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Crossref
reference URL
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7 January 2021
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Do Creutzfeldt-Jakob disease patients of Jewish Libyan origin have unique clinical features?
1 reference
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Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
Creutzfeldt-Jakob disease profile in patients homozygous for the PRNP E200K mutation
1 reference
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Crossref
reference URL
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7 January 2021
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The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease.
1 reference
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Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein gene.
1 reference
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Crossref
reference URL
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7 January 2021
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Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.
1 reference
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Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
Demyelinating peripheral neuropathy in Creutzfeldt-Jakob disease
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease.
1 reference
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Crossref
reference URL
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7 January 2021
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Genetic influence on the structural variations of the abnormal prion protein
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Klinische und genealogische Beobachtungen bei einem Fall von spastischer Pseudosklerose Jakobs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a PRNP gene mutation in Jakob's original Creutzfeldt-Jakob disease family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Codon 178 mutation of the human prion protein gene in a German family (Backer family): sequencing data from 72-year-old celloidin-embedded brain tissue
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Creutzfeldt-Jakob disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Descriptive epidemiology of Creutzfeldt-Jakob disease in Finland.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The familial occurrence of Creutzfeldt-Jakob disease and Alzheimer's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Creutzfeldt-Jakob disease with extensive degeneration of white matter. Ultrastructure of peripheral nerve.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification in Israel of 2 Jewish Creutzfeld-Jakob disease patients with a 178 mutation at their PrP gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Creutzfeldt-Jakob disease associated with a point mutation at codon 210 of the prion protein gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited prion disease caused by the V210I mutation: transmission to transgenic mice.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Panencephalitic Creutzfeldt-Jakob disease in a Chinese family. Unusual presentation with PrP codon 210 mutation and identification by PCR-SSCP.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial spongiform encephalopathy associated with a novel prion protein gene mutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Double mutations at codon 180 and codon 232 of the PRNP gene in an apparently sporadic case of Creutzfeldt-Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel prion protein gene mutation in an octogenarian with Creutzfeldt-Jakob disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Insertion in prion protein gene in familial Creutzfeldt-Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A prion disease with a novel 96-base pair insertional mutation in the prion protein gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new (two-repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Huntington disease phenocopy is a familial prion disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two novel insertions in the prion protein gene in patients with late-onset dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prion disease with 144 base pair insertion in a Japanese family line
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gerstmann-Sträussler-Scheinker disease and the Indiana kindred
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion in prion protein gene in a Moroccan family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions in the prion protein gene are not associated with CJD.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Conclusions of the symposium
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel twelve-generation kindred of fatal familial insomnia from germany representing the entire spectrum of disease expression.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal familial insomnia: clinical, neuropathological, and genetic description of a Spanish family.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal familial insomnia in a new Italian kindred.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sleep-wake cycle abnormalities in fatal familial insomnia. Evidence of the role of the thalamus in sleep regulation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dissociated 24-hour patterns of somatotropin and prolactin in fatal familial insomnia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive disruption of the circadian rhythm of melatonin in fatal familial insomnia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiovascular dysautonomia in fatal familial insomnia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebral metabolism in fatal familial insomnia: relation to duration, neuropathology, and distribution of protease-resistant prion protein.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
[18F]FDG PET in fatal familial insomnia: the functional effects of thalamic lesions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal familial insomnia: clinical and pathologic study of five new cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regional distribution of protease-resistant prion protein in fatal familial insomnia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900065-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0272-2712(02)00065-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
PubMed publication ID
12733424
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12733424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
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