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The genetics and neuropathology of Parkinson's disease
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scholarly article
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stated in
PubMed
title
The genetics and neuropathology of Parkinson's disease
(English)
1 reference
stated in
PubMed
main subject
Parkinson's disease
1 reference
based on heuristic
inferred from title
author
Henry Houlden
series ordinal
1
0 references
Andrew Singleton
series ordinal
2
object named as
Andrew B. Singleton
1 reference
stated in
Crossref
language of work or name
English
1 reference
stated in
PubMed
publication date
September 2012
1 reference
stated in
PubMed
published in
Acta Neuropathologica
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stated in
PubMed
volume
124
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stated in
PubMed
issue
3
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stated in
PubMed
page(s)
325-38
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stated in
PubMed
cites work
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee
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21 March 2017
A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease
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21 March 2017
A two-stage meta-analysis identifies several new loci for Parkinson's disease
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21 March 2017
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease
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PubMed Central
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21 March 2017
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
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21 March 2017
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update
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21 March 2017
PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1
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21 March 2017
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease
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21 March 2017
Genome-wide association study reveals genetic risk underlying Parkinson's disease
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PubMed Central
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21 March 2017
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
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PubMed Central
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21 March 2017
Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy
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PubMed Central
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21 March 2017
High-resolution whole-genome association study of Parkinson disease.
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21 March 2017
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
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21 March 2017
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
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21 March 2017
alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies
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PubMed Central
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21 March 2017
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
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PubMed Central
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21 March 2017
alpha-Synuclein locus triplication causes Parkinson's disease
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PubMed Central
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21 March 2017
Alpha-synuclein in Lewy bodies
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21 March 2017
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
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PubMed Central
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21 March 2017
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
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PubMed Central
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21 March 2017
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
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21 March 2017
Lewy bodies and parkinsonism in families with parkin mutations
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PubMed Central
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21 March 2017
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome
1 reference
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PubMed Central
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21 March 2017
Translation initiator EIF4G1 mutations in familial Parkinson disease
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PubMed Central
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21 March 2017
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome
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PubMed Central
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21 March 2017
A common LRRK2 mutation in idiopathic Parkinson's disease
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PubMed Central
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21 March 2017
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
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PubMed Central
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21 March 2017
Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications
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PubMed Central
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21 March 2017
Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration
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PubMed Central
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21 March 2017
Parkinson disease in twins: an etiologic study
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21 March 2017
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
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21 March 2017
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23
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PubMed Central
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21 March 2017
CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1
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PubMed Central
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21 March 2017
A large kindred with autosomal dominant Parkinson's disease
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PubMed Central
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21 March 2017
The mystery of missing heritability: Genetic interactions create phantom heritability
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21 March 2017
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data
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21 March 2017
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
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7 April 2017
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
1 reference
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7 April 2017
Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin
1 reference
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PubMed Central
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7 April 2017
The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia
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7 April 2017
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
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7 April 2017
PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy
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7 April 2017
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
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7 April 2017
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
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7 April 2017
Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin
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7 April 2017
Alpha-synuclein locus duplication as a cause of familial Parkinson's disease
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7 April 2017
VPS35 mutations in Parkinson disease
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PubMed Central
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28 September 2017
Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α-synuclein triplication (Iowa kindred).
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28 September 2017
Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson's disease
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PubMed Central
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28 September 2017
Heritability of Parkinson disease in Swedish twins: a longitudinal study
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PubMed Central
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28 September 2017
Novel histopathologic findings in molecularly-confirmed pantothenate kinase-associated neurodegeneration
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28 September 2017
Genome-wide association study confirms extant PD risk loci among the Dutch
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28 September 2017
Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations
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28 September 2017
Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation
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PubMed Central
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28 September 2017
Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35).
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PubMed Central
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28 September 2017
Expanding the clinical phenotype of SNCA duplication carriers
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PubMed Central
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28 September 2017
SNCA variants are associated with increased risk for multiple system atrophy
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
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28 September 2017
DCTN1 mutations in Perry syndrome
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28 September 2017
The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study
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PubMed Central
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28 September 2017
Genomewide association study for susceptibility genes contributing to familial Parkinson disease
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28 September 2017
The spectrum of parkinsonian manifestations associated with glucocerebrosidase mutations
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28 September 2017
Familial parkinsonism: study of original Sagamihara PARK8 (I2020T) kindred with variable clinicopathologic outcomes
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28 September 2017
Characterization of PLA2G6 as a locus for dystonia-parkinsonism
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28 September 2017
Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays
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PubMed Central
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28 September 2017
Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN).
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28 September 2017
SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia
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PubMed Central
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28 September 2017
Mutations in LRRK2 as a cause of Parkinson's disease
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PubMed Central
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28 September 2017
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
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28 September 2017
G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
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28 September 2017
PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
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28 September 2017
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data
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28 September 2017
The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases
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PubMed Central
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28 September 2017
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations
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28 September 2017
Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews
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28 September 2017
Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).
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28 September 2017
Somatic NF1 mutation spectra in a family with neurofibromatosis type 1: toward a theory of genetic modifiers
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28 September 2017
How much phenotypic variation can be attributed to parkin genotype?
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 September 2017
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 September 2017
Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 September 2017
Concurrence of alpha-synuclein and tau brain pathology in the Contursi kindred
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 September 2017
A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 September 2017
Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 September 2017
Hereditary form of parkinsonism--dementia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 September 2017
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 September 2017
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 September 2017
Occurrence of Parkinson's syndrome in type I Gaucher disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 September 2017
Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
31 May 2018
Clinical and pathological features of a Parkinsonian syndrome in a family with an Ala53Thr alpha-synuclein mutation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
31 May 2018
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
31 May 2018
Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
31 May 2018
Filamentous alpha-synuclein inclusions link multiple system atrophy with Parkinson's disease and dementia with Lewy bodies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
31 May 2018
Hereditary Mental Depression and Parkinsonism With Taurine Deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
31 May 2018
Kin-cohort analysis of LRRK2-G2019S penetrance in Parkinson's disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
PINK1-linked parkinsonism is associated with Lewy body pathology.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
ATP13A2 variants in early-onset Parkinson's disease patients and controls
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Clinical heterogeneity and genotype-phenotype correlations in hereditary spastic paraplegia because of Spatacsin mutations (SPG11).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
PARK9-LINKED PARKINSONISM IN EASTERN ASIA: MUTATION DETECTION IN ATP13A2 AND CLINICAL PHENOTYPE
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
PINK1 mutation in Taiwanese early-onset parkinsonism : clinical, genetic, and dopamine transporter studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Heterozygousparkinpoint mutations are as common in control subjects as in Parkinson's patients
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Lrrk2 and Lewy body disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Dopa-responsive dystonia and early-onset Parkinson's disease in a patient with GTP cyclohydrolase I deficiency?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
The parkinsonian phenotype of spinocerebellar ataxia type 3 in a Taiwanese family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Alpha-synuclein in blood and brain from familial Parkinson disease with SNCA locus triplication
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Parkin variants in North American Parkinson's disease: cases and controls.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
A clinical-genetic study of Parkinson’s disease in a genetically isolated community
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
The role of pathogenic DJ-1 mutations in Parkinson's disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Gaucher disease with parkinsonian manifestations: does glucocerebrosidase deficiency contribute to a vulnerability to parkinsonism?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Parkinson's syndrome preceding clinical manifestation of Gaucher's disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589971
retrieved
28 November 2018
Whole gene deletion and splicing mutations expand the PINK1 genotypic spectrum
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Clinicopathologic study of a SNCA gene duplication patient with Parkinson disease and dementia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Homozygosity mapping through whole genome analysis identifies a COL18A1 mutation in an Indian family presenting with an autosomal recessive neurological disorder
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Gaucher disease and parkinsonism: a phenotypic and genotypic characterization
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Role of parkin mutations in 111 community-based patients with early-onset parkinsonism
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Screening PARK genes for mutations in early-onset Parkinson's disease patients from Queensland, Australia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Parkin-positive autosomal recessive juvenile Parkinsonism with alpha-synuclein-positive inclusions
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Parkinson's disease and dementia with Lewy bodies: a difference in dose?
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Variable expression of neurofibromatosis 1 in monozygotic twins
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22806825
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/S00401-012-1013-5
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
558255
Dimensions Publication ID
1007870763
0 references
Fatcat ID
release_cxut2mph2bgcvjl4jmjjkty4du
0 references
OpenCitations bibliographic resource ID
558255
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
558255
PMC publication ID
3589971
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
558255
PubMed publication ID
22806825
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
558255
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