(Q33351731)

26 July 2017

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title

The curious case of phenocopies in families with genetic Parkinson's disease (English)

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26 July 2017

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Anthony E Lang

4

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Christine Klein

series ordinal

1

object named as

Christine Klein

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PubMed ID

21735483

Connie Fernández-Cid Marras

26 July 2017

series ordinal

3

object named as

Connie Marras

1 reference

26 July 2017

Rosalind Chuang

2

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PubMed ID

21735483

26 July 2017

language of work or name

English

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publication date

6 July 2011

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26 July 2017

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26 July 2017

26

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26 July 2017

10

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26 July 2017

1793-1802

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Parkinson disease, 10 years after its genetic revolution: multiple clues to a complex disorder

26 July 2017

1 reference

Pathogenesis of familial Parkinson's disease: new insights based on monogenic forms of Parkinson's disease

21 January 2018

1 reference

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

21 January 2018

1 reference

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

21 January 2018

1 reference

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

21 January 2018

1 reference

Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism

21 January 2018

1 reference

Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers

21 January 2018

1 reference

Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients

21 January 2018

1 reference

The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval

21 January 2018

1 reference

Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein

21 January 2018

1 reference

Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease.

21 January 2018

1 reference

parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease.

21 January 2018

1 reference

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

21 January 2018

1 reference

Prevalence of Parkinson's disease in Cantalejo, Spain: a door-to-door survey.

21 January 2018

1 reference

Prevalence of Parkinson's disease in Junín, Buenos Aires Province, Argentina

21 January 2018

1 reference

Prevalence of Parkinson's disease and other types of parkinsonism: a door-to-door survey in three Sicilian municipalities. The Sicilian Neuro-Epidemiologic Study (SNES) Group

21 January 2018

1 reference

Prevalence of Parkinson disease in Singapore: Chinese vs Malays vs Indians

21 January 2018

1 reference

Parkinson's disease in Kin-Hu, Kinmen: a community survey by neurologists

21 January 2018

1 reference

LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8.

21 January 2018

1 reference

Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease

21 January 2018

1 reference

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

21 January 2018

1 reference

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

21 January 2018

1 reference

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2

21 January 2018

1 reference

Digenic parkinsonism: investigation of the synergistic effects of PRKN and LRRK2.

21 January 2018

1 reference

Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism

21 January 2018

1 reference

Prevalence and clinical features of LRRK2 mutations in patients with Parkinson's disease in southern Spain.

21 January 2018

1 reference

Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's disease

21 January 2018

1 reference

Assortative Mating in Schizophrenia: Results from the Copenhagen High-Risk Study

21 January 2018

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The personality associated with Parkinson's disease

21 January 2018

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Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria

21 January 2018

1 reference

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

1 reference

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

21 January 2018

1 reference

LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance

21 January 2018

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Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

21 January 2018

1 reference

Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.

21 January 2018

1 reference

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

21 January 2018

1 reference

Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease

21 January 2018

1 reference

Heterogeneity within a large kindred with frontotemporal dementia: A novel progranulin mutation

21 January 2018

1 reference

21 January 2018

Lrrk2 in the limelight!

1 reference

Are interruptedSCA2CAG repeat expansions responsible for parkinsonism?

21 January 2018

1 reference

Lrrk2 pathogenic substitutions in Parkinson's disease

21 January 2018

1 reference

Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.23853

1 reference

26 July 2017

1 reference

PubMed ID

21735483