(Q46027013)

English

The leucine rich repeat kinase 2 (LRRK2) G2019S substitution mutation. Association with Parkinson disease, malignant melanoma and prevalence in ethnic groups in Israel.

scientific article published on 24 March 2009

The leucine rich repeat kinase 2 (LRRK2) G2019S substitution mutation

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

The leucine rich repeat kinase 2 (LRRK2) G2019S substitution mutation. Association with Parkinson disease, malignant melanoma and prevalence in ethnic groups in Israel. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

0 references

Parkinson's disease

1 reference

based on heuristic

inferred from title

Sharon Hassin-Baer

object named as

Sharon Hassin-Baer

1

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2

object named as

Yael Laitman

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

author name string

Esther Azizi

3

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

Irena Molchadski

4

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

Gilli Galore-Haskel

5

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

Frida Barak

6

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

Oren S Cohen

7

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

Eitan Friedman

8

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

publication date

24 March 2009

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

Journal of Neurology

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

256

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

3

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

483-487

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

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

1 reference

https://api.crossref.org/works/10.1007%2FS00415-009-0117-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00415-009-0117-X

21 January 2018

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

1 reference

https://api.crossref.org/works/10.1007%2FS00415-009-0117-X

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Malignant melanoma in early Parkinson's disease: the DATATOP trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common LRRK2 mutation in idiopathic Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical characteristics of Parkinson's disease among Jewish Ethnic groups in Israel

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of Parkinson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Are Parkinson disease patients protected from some but not all cancers?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

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

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parkinsonism: onset, progression, and mortality. 1967.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Malignant Melanoma and Other Types of Cancer Preceding Parkinson Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical cancer pattern in patients with Parkinson's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19412725

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

https://pubmed.ncbi.nlm.nih.gov/19412725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00415-009-0117-X

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19412725

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