(Q34300290)

1 August 2017

title

Clinical expression of LRRK2 G2019S mutations in the elderly (English)

1 reference

1 August 2017

author

Rachel Saunders-Pullman

series ordinal

9

object named as

Rachel Saunders-Pullman

1 reference

1 August 2017

2

Richard B Lipton

1 reference

1 August 2017

7

Laurie J Ozelius

1 reference

1 August 2017

8

Susan B Bressman

1 reference

1 August 2017

3

Cuiling Wang

1 reference

1 August 2017

4

Mindy Katz

1 reference

1 August 2017

Marta San Luciano

1

1 reference

1 August 2017

Molly E Zimmerman

series ordinal

5

1 reference

1 August 2017

Amy E Sanders

series ordinal

6

1 reference

1 August 2017

language of work or name

English

0 references

publication date

1 November 2010

1 reference

1 August 2017

1 reference

1 August 2017

volume

25

1 reference

1 August 2017

issue

15

1 reference

1 August 2017

page(s)

2571-2576

1 reference

Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: a systematic review.

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

The LRRK2 G2019S mutation as the cause of Parkinson's disease in Ashkenazi Jews

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

The Trail Making Test and its neurobehavioral components

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

The premotor phase of Parkinson's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

Biochemical and pathological characterization of Lrrk2.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

A common LRRK2 mutation in idiopathic Parkinson's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

Screening for Dementia by Telephone Using the Memory Impairment Screen

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

The geometric structure, construction, and interpretation of path-following (trail-making) tests

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

The Clinical Dementia Rating (CDR): current version and scoring rules

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

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

6 July 2018

1 reference

Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries

21 January 2018

1 reference

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

21 January 2018

1 reference

A new clinical scale for the staging of dementia.

21 January 2018

1 reference

Abnormality of gait as a predictor of non-Alzheimer's dementia.

21 January 2018

1 reference

Prevalence of parkinsonian signs and associated mortality in a community population of older people.

21 January 2018

1 reference

Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease

21 January 2018

1 reference

Genetic screening for LRRK2 gene G2019S mutation in Parkinson's disease patients from Southern Italy

21 January 2018

1 reference

LRRK2 and GBA mutations differentially affect the initial presentation of Parkinson disease.

21 January 2018

1 reference

Lrrk2 and Lewy body disease

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

Prevalence of Parkinson's disease in Europe: A collaborative study of population-based cohorts. Neurologic Diseases in the Elderly Research Group

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

Prevalence of Parkinson's disease in the elderly: The Rotterdam Study

28 October 2018

1 reference

A population perspective on diagnostic criteria for Parkinson's disease.

21 January 2018

1 reference

Clinical Heterogeneity of the LRRK2 G2019S Mutation

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978804

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

28 October 2018

1 reference

Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementia

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20721910

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20721910

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/MDS.23330

1 reference

1 August 2017

1 reference

1 August 2017

1 reference