(Q33723751)

28 July 2017

title

Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease (English)

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28 July 2017

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Stanley Fahn

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Elan D Louis

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Andrew Siderowf

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Joseph H Friedman

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Caroline Tanner

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Roy N Alcalay

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Steven J Frucht

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ORCID Public Data File 2021

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Miguel Verbitsky

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Sergey Kisselev

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Blair Ford

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Karen S Marder

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2

Helen Mejia-Santana

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Ruth Ottman

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Susan Bressman

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Lucien J Cote

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Lorraine N Clark

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3

Ming Xin Tang

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Cynthia L Comella

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Cheryl H Waters

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28 July 2017

Llency Rosado

4

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28 July 2017

Barbara M Ross

7

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28 July 2017

Amy Colcher

10

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Danna Jennings

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28 July 2017

Martha A Nance

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28 July 2017

William K Scott

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Susan F Mickel

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28 July 2017

Howard F Andrews

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28 July 2017

Michael Rezak

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Kevin Novak

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Ronald Pfeiffer

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28 July 2017

Laura Marsh

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Bradley Hiner

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Elise Caccappolo

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28 July 2017

publication date

1 December 2009

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28 July 2017

published in

Archives of Neurology

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28 July 2017

volume

66

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28 July 2017

issue

12

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28 July 2017

page(s)

1517-1522

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

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Prognostic factors for the progression of Parkinson's disease: a systematic review

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Clinical diagnostic criteria for dementia associated with Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Cognitive impairment in Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Changes in motor subtype and risk for incident dementia in Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Motor subtype and cognitive decline in Parkinson's disease, Parkinson's disease with dementia, and dementia with Lewy bodies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Variable expression of Parkinson's disease: a base-line analysis of the DATATOP cohort. The Parkinson Study Group

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Tremor dominant parkinsonism: Clinical description and LRRK2 mutation screening.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Frequency of LRRK2 mutations in early- and late-onset Parkinson disease

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

LRRK2 gene and tremor-dominant parkinsonism.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Extrapyramidal features in Parkinson's disease with and without dementia and dementia with Lewy bodies: A cross-sectional comparative study

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

A genetic profile of contemporary Jewish populations

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Clinical Heterogeneity of the LRRK2 G2019S Mutation

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Clinicogenetic study of mutations inLRRK2 exon 41 in Parkinson's disease patients from 18 countries

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

LRRK2 gene in Parkinson disease: Mutation analysis and case control association study

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2837584

Familial aggregation of early- and late-onset Parkinson's disease

30 October 2018

1 reference

12 December 2020

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

1 reference

12 December 2020

Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease

1 reference

12 December 2020

LRRK2 G2019S mutation and Parkinson's disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sample

1 reference

12 December 2020

10.1001/ARCHNEUROL.2009.267

Identifiers

DOI

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28 July 2017

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28 July 2017

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