(Q44195128)

30 November 2017

1 reference

title

Genetic epidemiology of Parkinson's disease (English)

1 reference

30 November 2017

1 reference

1 reference

H Payami

1

1 reference

PubMed ID

9877530

30 November 2017

S Zareparsi

series ordinal

2

1 reference

30 November 2017

1 January 1998

1 reference

Journal of Geriatric Psychiatry and Neurology

30 November 2017

1 reference

30 November 2017

11

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30 November 2017

98-106

1 reference

30 November 2017

2

1 reference

Prevalence of Parkinson's disease in the biracial population of Copiah County, Mississippi.

30 November 2017

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Parkinson's disease in twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Twin studies and the genetics of Parkinson's disease--a reappraisal

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Parkinson's disease in twins studied with 18F-dopa and positron emission tomography

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Environmental antecedents of young-onset Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Environmental and genetic risk factors in Parkinson's disease: a case-control study in southern Italy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Risk of Parkinson's disease among first-degree relatives: A community-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

A clinical and genetic study of familial cases of Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Autosomal dominant Lewy body parkinsonism in a four-generation family

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Familial parkinsonism: Our experience and review

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Clinical genetic analysis of Parkinson's disease in the Contursi kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Familial autosomal dominant dopa responsive Parkinson's disease in three living generations showing extreme anticipation and childhood onset

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

A clinical genetic study of Parkinson's disease: evidence for dominant transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Genetic anticipation in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Anticipation in familial Parkinson's disease: a reanalysis of 13 United Kingdom kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Triplet repeat gene sequences in neuropsychiatric diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Advances in our understanding of the mechanisms of the neurotoxicity of MPTP and related compounds

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Chronic nicotine intake decelerates aging of nigrostriatal dopaminergic neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

A genetic polymorphism of MAO-B modifies the association of cigarette smoking and Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Low frequency of alpha-synuclein mutations in familial Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Absence of mutations in the coding region of the alpha-synuclein gene in pathologically proven Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Molecular cloning of cDNA encoding an unrecognized component of amyloid in Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Alpha-synuclein in Lewy bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Familial juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

An early cytoplasmic change before Lewy body maturation: an ultrastructural study of the substantia nigra from an autopsy case of juvenile parkinsonism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Ecogenetics of Parkinson's disease: 4-hydroxylation of debrisoquine

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Familial Parkinson's disease and polymorphism at the CYP2D6 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

The CYP2D6B mutant allele is overrepresented in the Lewy body variant of Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Genetic variability of the CYP 2D6 gene is not a risk factor for sporadic Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

The dopamine transporter gene and Parkinson's disease in a Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Clinicopathological aspects of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Extrapyramidalism in Alzheimer's disease: prevalence, psychiatric, and neuropsychological correlates

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

A clinicopathologic study of 100 cases of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part IX. A prospective cliniconeuropathologic study of Parkinson's features in Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Apolipoprotein E in animal models of CNS injury and in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Genetic dissection of Alzheimer disease, a heterogeneous disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Apolipoprotein E genes in Lewy body and Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Senile dementia of the Lewy body type has an apolipoprotein E epsilon 4 allele frequency intermediate between controls and Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Apolipoprotein E is present in hippocampal neurons without neurofibrillary tangles in Alzheimer's disease and in age-matched controls.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Apo E genotypes in multiple sclerosis, Parkinson's disease, schwannomas and late-onset Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Association of apolipoprotein epsilon 4 allele and neuropathologic findings in patients with dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Frequency of the apolipoprotein E epsilon 4 allele in a case-control study of early onset Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Genetic association between susceptibility to Parkinson's disease and alpha1-antichymotrypsin polymorphism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

APOE*4-associated Alzheimer's disease risk is modified by alpha 1-antichymotrypsin polymorphism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Coiled bodies and gems: Janus or gemini?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Origin and functional consequences of the complex I defect in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

The Familial Occurrence of Parkinson's Disease Lack of Evidence for Maternal Inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Maternal inheritance in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Genetic Complexity and Parkinson's Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

Identification of Spanish familial Parkinson's disease and screening for the Ala53Thr mutation of the α-synuclein gene in early onset patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

No Association between Parkinson's Disease and Low-Activity Alleles of CatecholO-Methyltransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100207

10.1177/089198879801100207

21 January 2018

Identifiers

DOI

1 reference

30 November 2017

1 reference

PubMed ID

9877530