Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 8

1.

Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease.

Lesage S, Condroyer C, Lannuzel A, Lohmann E, Troiano A, Tison F, Damier P, Thobois S, Ouvrard-Hernandez AM, Rivaud-Péchoux S, Brefel-Courbon C, Destée A, Tranchant C, Romana M, Leclere L, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group.

J Med Genet. 2009 Jul;46(7):458-64. doi: 10.1136/jmg.2008.062612. Epub 2009 Apr 8.

PMID:
19357115
[PubMed - indexed for MEDLINE]
2.

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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
4.

PARK8 LRRK2 parkinsonism.

Haugarvoll K, Wszolek ZK.

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

PMID:
16822348
[PubMed - indexed for MEDLINE]
5.

Biochemical and molecular features of LRRK2 and its pathophysiological roles in Parkinson's disease.

Seol W.

BMB Rep. 2010 Apr;43(4):233-44. Review.

PMID:
20423607
[PubMed - indexed for MEDLINE]
Free Article
6.

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
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
8.

Autosomal dominant Parkinson's disease.

Sundal C, Fujioka S, Uitti RJ, Wszolek ZK.

Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S7-10. doi: 10.1016/S1353-8020(11)70005-0. Review.

PMID:
22166459
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk