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Results: 16

1.

The importance of rare DNA variation in neurologic disease: cautionary tale.

Haines JL.

Neurology. 2013 Mar 12;80(11):974-5. doi: 10.1212/WNL.0b013e318287289c. Epub 2013 Feb 13.

PMID:
23408868
[PubMed - indexed for MEDLINE]
2.

Genetics of Parkinson disease and other movement disorders.

Kumar KR, Lohmann K, Klein C.

Curr Opin Neurol. 2012 Aug;25(4):466-74. doi: 10.1097/WCO.0b013e3283547627. Review.

PMID:
22772876
[PubMed - indexed for MEDLINE]
3.

Role of mendelian genes in "sporadic" Parkinson's disease.

Lesage S, Brice A.

Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S66-70. doi: 10.1016/S1353-8020(11)70022-0. Review.

PMID:
22166458
[PubMed - indexed for MEDLINE]
4.

In search of genes involved in neurodegenerative disorders.

Pardo LM, van Duijn CM.

Mutat Res. 2005 Dec 30;592(1-2):89-101. Epub 2005 Jul 11. Review.

PMID:
16009383
[PubMed - indexed for MEDLINE]
5.

Genetics of Parkinson disease.

Pankratz N, Foroud T.

NeuroRx. 2004 Apr;1(2):235-42. Review.

PMID:
15717024
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Next-generation sequencing to identify genetic causes of cardiomyopathies.

Norton N, Li D, Hershberger RE.

Curr Opin Cardiol. 2012 May;27(3):214-20. doi: 10.1097/HCO.0b013e328352207e. Review.

PMID:
22421630
[PubMed - indexed for MEDLINE]
7.

Advances in the genetics of Parkinson's disease.

Rosner S, Giladi N, Orr-Urtreger A.

Acta Pharmacol Sin. 2008 Jan;29(1):21-34. Review.

PMID:
18158863
[PubMed - indexed for MEDLINE]
Free Article
8.

[Genetic basis of sponadic Parkinson disease: common disease-multiple rare variants].

Mitsui J.

Rinsho Shinkeigaku. 2010 Nov;50(11):865-6. Review. Japanese. No abstract available.

PMID:
21921476
[PubMed - indexed for MEDLINE]
9.

Etiology and pathophysiology of frontotemporal dementia, Parkinson disease and Alzheimer disease: lessons from genetic studies.

Wider C, Wszolek ZK.

Neurodegener Dis. 2008;5(3-4):122-5. doi: 10.1159/000113680. Epub 2008 Mar 6. Review.

PMID:
18322368
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Molecular pathways in sporadic PD.

Valente EM, Arena G, Torosantucci L, Gelmetti V.

Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S71-3. doi: 10.1016/S1353-8020(11)70023-2. Review.

PMID:
22166460
[PubMed - indexed for MEDLINE]
11.

Exome sequencing as a tool for Mendelian disease gene discovery.

Bamshad MJ, Ng SB, Bigham AW, Tabor HK, Emond MJ, Nickerson DA, Shendure J.

Nat Rev Genet. 2011 Sep 27;12(11):745-55. doi: 10.1038/nrg3031. Review.

PMID:
21946919
[PubMed - indexed for MEDLINE]
12.

[Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].

Hattori N.

Rinsho Shinkeigaku. 2004 Apr-May;44(4-5):241-62. Review. Japanese.

PMID:
15287506
[PubMed - indexed for MEDLINE]
13.

Genetics of Parkinson's disease.

Bonifati V.

Minerva Med. 2005 Jun;96(3):175-86. Review.

PMID:
16175160
[PubMed - indexed for MEDLINE]
14.

The genetics of Parkinson disease: Implications for neurological care.

Klein C, Schlossmacher MG.

Nat Clin Pract Neurol. 2006 Mar;2(3):136-46. Review.

PMID:
16932540
[PubMed - indexed for MEDLINE]
15.

The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.

Jensen HK.

Dan Med Bull. 2002 Nov;49(4):318-45. Review.

PMID:
12553167
[PubMed - indexed for MEDLINE]
16.

What genetics tells us about the causes and mechanisms of Parkinson's disease.

Corti O, Lesage S, Brice A.

Physiol Rev. 2011 Oct;91(4):1161-218. doi: 10.1152/physrev.00022.2010. Review.

PMID:
22013209
[PubMed - indexed for MEDLINE]
Free Article

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