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Results: 7

Related Articles by Review for PubMed (Select 16436782)

1.

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

Ozelius LJ, Senthil G, Saunders-Pullman R, Ohmann E, Deligtisch A, Tagliati M, Hunt AL, Klein C, Henick B, Hailpern SM, Lipton RB, Soto-Valencia J, Risch N, Bressman SB.

N Engl J Med. 2006 Jan 26;354(4):424-5. No abstract available.

2.

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

Thaler A, Ash E, Gan-Or Z, Orr-Urtreger A, Giladi N.

J Neural Transm. 2009 Nov;116(11):1473-82. doi: 10.1007/s00702-009-0303-0. Review.

PMID:
19756366
3.

LRRK2 in Parkinson's disease: genetic and clinical studies from patients.

Kumari U, Tan EK.

FEBS J. 2009 Nov;276(22):6455-63. doi: 10.1111/j.1742-4658.2009.07344.x. Epub 2009 Oct 5. Review.

PMID:
19804413
4.

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

Correia Guedes L, Ferreira JJ, Rosa MM, Coelho M, Bonifati V, Sampaio C.

Parkinsonism Relat Disord. 2010 May;16(4):237-42. doi: 10.1016/j.parkreldis.2009.11.004. Epub 2009 Nov 30. Review.

PMID:
19945904
5.

Mutations in LRRK2 as a cause of Parkinson's disease.

Giasson BI, Van Deerlin VM.

Neurosignals. 2008;16(1):99-105. Epub 2007 Dec 5. Review.

PMID:
18097165
6.

The pleomorphic pathology of inherited Parkinson's disease: lessons from LRRK2.

Bonifati V.

Curr Neurol Neurosci Rep. 2006 Sep;6(5):355-7. Review. No abstract available.

PMID:
16928343
7.

The importance of LRRK2 mutations in Parkinson disease.

Schapira AH.

Arch Neurol. 2006 Sep;63(9):1225-8. Review. No abstract available.

PMID:
16966498
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