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Genetics of dementia
scientific article published in The Lancet
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
title
Genetics of dementia
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
main subject
dementia
0 references
author
Peter R Schofield
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
John B Kwok
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
author name string
Clement T Loy
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
Anne M Turner
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
language of work or name
English
0 references
publication date
6 August 2013
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
volume
383
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
issue
9919
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
page(s)
828-840
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
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7 January 2021
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APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
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7 January 2021
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Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland
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Frequency of mutations in the presenilin and amyloid precursor protein genes in early-onset Alzheimer disease in Spain.
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Extreme cerebrospinal fluid amyloid beta levels identify family with late-onset Alzheimer's disease presenilin 1 mutation.
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Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families
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Sequence analysis of presenilin-1 gene mutation in Japanese Alzheimer's disease patients.
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Correlating familial Alzheimer's disease gene mutations with clinical phenotype
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Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
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Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
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Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP
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Genetics of dementia
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Alzheimer's disease
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Variant of TREM2 Associated with the Risk of Alzheimer's Disease
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Mutations in TREM2 lead to pure early-onset dementia without bone cysts.
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Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review
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Neuroimaging in frontotemporal lobar degeneration--predicting molecular pathology
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Clinicopathological correlates in frontotemporal dementia
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7 January 2021
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Phenotypic signatures of genetic frontotemporal dementia
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7 January 2021
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The logopenic variant of primary progressive aphasia
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Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
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Semantic dementia: demography, familial factors and survival in a consecutive series of 100 cases
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7 January 2021
based on heuristic
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TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia
1 reference
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7 January 2021
based on heuristic
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Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathology.
1 reference
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https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
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Genetic causes of frontotemporal degeneration
1 reference
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7 January 2021
based on heuristic
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Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features
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7 January 2021
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The heritability and genetics of frontotemporal lobar degeneration.
1 reference
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https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
1 reference
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7 January 2021
based on heuristic
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Tau alteration and neuronal degeneration in tauopathies: mechanisms and models
1 reference
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https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
1 reference
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https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Potential mechanisms of progranulin-deficient FTLD
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
1 reference
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https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for an oligogenic basis of amyotrophic lateral sclerosis
1 reference
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https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Pick bodies in a family with presenilin-1 Alzheimer's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
TARDBP mutations in frontotemporal lobar degeneration: frequency, clinical features, and disease course.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An algorithm for genetic testing of frontotemporal lobar degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropsychological deficits in frontotemporal dementia and Alzheimer's disease: a meta-analytic review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial aggregation in frontotemporal dementia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transmissible spongiform encephalopathies.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prion disease genetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amyloid imaging in distinguishing atypical prion disease from Alzheimer disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The natural history of Alzheimer disease: a longitudinal presymptomatic and symptomatic study of a familial cohort.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of Huntington's disease decades before diagnosis: the Predict-HD study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Levodopa responsive parkinsonism in an adult with Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The autosomal recessive cerebellar ataxias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cognitive findings in spinocerebellar ataxia type 2: relationship to genetic and clinical variables.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cognitive deficits in Machado-Joseph disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dentatorubral-pallidoluysian atrophy or Naito-Oyanagi disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cognitive functioning in neurologically symptomatic and asymptomatic forms of Wilson's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical molecular diagnosis of Wilson disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Wilson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The adult form of Niemann-Pick disease type C.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New agents and approaches to treatment in Niemann-Pick type C disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic disorders affecting white matter in the pediatric age.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CADASIL
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individuals
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Complex single gene disorders and epilepsy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in DNAJC5, encoding cysteine-string protein alpha, cause autosomal-dominant adult-onset neuronal ceroid lipofuscinosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single-gene neurological disorders in South Wales: an epidemiological study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recent advances in the genetics of dementia with lewy bodies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial aggregation of dementia with Lewy bodies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of families with cortical Lewy body disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dementia in Parkinson's disease: a 20-year neuropsychological study (Sydney Multicentre Study).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genetics of Parkinson's syndromes: a critical review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glucocerebrosidase mutations are an important risk factor for Lewy body disorders.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetics of dementia: update and guidelines for the clinician
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
International Huntington Association and the World Federation of Neurology Research Group on Huntington's Chorea. Guidelines for the molecular genetics predictive test in Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Columbia-Suicide Severity Rating Scale: initial validity and internal consistency findings from three multisite studies with adolescents and adults
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exome sequencing as a tool for Mendelian disease gene discovery
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exome sequencing reveals VCP mutations as a cause of familial ALS
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Individual genomes on the horizon
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(13)60630-3
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
PubMed ID
23927914
1 reference
stated in
Europe PubMed Central
PubMed ID
23927914
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 March 2020
ResearchGate publication ID
255714414
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