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Items: 1 to 20 of 50

1.

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

Orr-Urtreger A, Shifrin C, Rozovski U, Rosner S, Bercovich D, Gurevich T, Yagev-More H, Bar-Shira A, Giladi N.

Neurology. 2007 Oct 16;69(16):1595-602.

PMID:
17938369
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 (Vienna). 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.

4.

Clinical features of LRRK2 parkinsonism.

Haugarvoll K, Wszolek ZK.

Parkinsonism Relat Disord. 2009 Dec;15 Suppl 3:S205-8. doi: 10.1016/S1353-8020(09)70815-6. Review.

PMID:
20082991
5.

LRRK2 G2019S in the North African population: a review.

Benamer HT, de Silva R.

Eur Neurol. 2010;63(6):321-5. doi: 10.1159/000279653. Epub 2010 Apr 23. Review.

6.

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
7.

Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson's disease.

Bardien S, Lesage S, Brice A, Carr J.

Parkinsonism Relat Disord. 2011 Aug;17(7):501-8. doi: 10.1016/j.parkreldis.2010.11.008. Review.

PMID:
21641266
8.

LRRK2 and Parkinson disease.

Dächsel JC, Farrer MJ.

Arch Neurol. 2010 May;67(5):542-7. doi: 10.1001/archneurol.2010.79. Review.

PMID:
20457952
9.

Genetic movement disorders in patients of Jewish ancestry.

Inzelberg R, Hassin-Baer S, Jankovic J.

JAMA Neurol. 2014 Dec;71(12):1567-72. doi: 10.1001/jamaneurol.2014.1364. Review.

PMID:
25347348
10.

PARK8 LRRK2 parkinsonism.

Haugarvoll K, Wszolek ZK.

Curr Neurol Neurosci Rep. 2006 Jul;6(4):287-94. Review.

PMID:
16822348
12.
13.

[Clinical molecular genetics for PARK8 (LRRK2)].

Tomiyama H, Hatano T, Hattori N.

Brain Nerve. 2007 Aug;59(8):839-50. Review. Japanese.

PMID:
17713120
14.

LRRK2 and vesicle trafficking.

Sanna G, Del Giudice MG, Crosio C, Iaccarino C.

Biochem Soc Trans. 2012 Oct;40(5):1117-22. Review.

PMID:
22988875
15.

Genetic factors and colorectal cancer in Ashkenazi Jews.

Locker GY, Lynch HT.

Fam Cancer. 2004;3(3-4):215-21. Review.

PMID:
15516844
16.

Quantitative assessment of the effect of LRRK2 exonic variants on the risk of Parkinson's disease: a meta-analysis.

Wu X, Tang KF, Li Y, Xiong YY, Shen L, Wei ZY, Zhou KJ, Niu JM, Han X, Yang L, Feng GY, He L, Qin SY.

Parkinsonism Relat Disord. 2012 Jul;18(6):722-30. doi: 10.1016/j.parkreldis.2012.04.013. Epub 2012 May 8. Review.

PMID:
22575234
17.

Co-occurrence of sporadic parkinsonism and late-onset Alzheimer's disease in a Brazilian male with the LRRK2 p.G2019S mutation.

Santos-Rebouças CB, Abdalla CB, Baldi FJ, Martins PA, Corrêa JC, Gonçalves AP, Cunha MS, Borges MB, Pereira JS, Laks J, Pimentel MM.

Genet Test. 2008 Dec;12(4):471-3. doi: 10.1089/gte.2008.0042. Review.

PMID:
19072560
18.

α-Synuclein, leucine-rich repeat kinase-2, and manganese in the pathogenesis of Parkinson disease.

Covy JP, Giasson BI.

Neurotoxicology. 2011 Oct;32(5):622-9. doi: 10.1016/j.neuro.2011.01.003. Epub 2011 Jan 14. Review.

19.

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
20.

TDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT.

Ling H, Kara E, Bandopadhyay R, Hardy J, Holton J, Xiromerisiou G, Lees A, Houlden H, Revesz T.

Neurobiol Aging. 2013 Dec;34(12):2889.e5-9. doi: 10.1016/j.neurobiolaging.2013.04.011. Epub 2013 May 9. Review.

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