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Results: 8

1.

Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease.

Martinez M, Brice A, Vaughan JR, Zimprich A, Breteler MM, Meco G, Filla A, Farrer MJ, Bétard C, Hardy J, De Michele G, Bonifati V, Oostra B, Gasser T, Wood NW, Dürr A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.

J Med Genet. 2004 Dec;41(12):900-7.

PMID:
15591275
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

How much phenotypic variation can be attributed to parkin genotype?

Lohmann E, Periquet M, Bonifati V, Wood NW, De Michele G, Bonnet AM, Fraix V, Broussolle E, Horstink MW, Vidailhet M, Verpillat P, Gasser T, Nicholl D, Teive H, Raskin S, Rascol O, Destée A, Ruberg M, Gasparini F, Meco G, Agid Y, Durr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.

Ann Neurol. 2003 Aug;54(2):176-85.

PMID:
12891670
[PubMed - indexed for MEDLINE]
3.

Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

Periquet M, Latouche M, Lohmann E, Rawal N, De Michele G, Ricard S, Teive H, Fraix V, Vidailhet M, Nicholl D, Barone P, Wood NW, Raskin S, Deleuze JF, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.

Brain. 2003 Jun;126(Pt 6):1271-8.

PMID:
12764050
[PubMed - indexed for MEDLINE]
Free Article
4.

New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism.

Rawal N, Periquet M, Lohmann E, Lücking CB, Teive HA, Ambrosio G, Raskin S, Lincoln S, Hattori N, Guimaraes J, Horstink MW, Dos Santos Bele W, Brousolle E, Destée A, Mizuno Y, Farrer M, Deleuze JF, De Michele G, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.

Neurology. 2003 Apr 22;60(8):1378-81.

PMID:
12707451
[PubMed - indexed for MEDLINE]
5.

PARK6 is a common cause of familial parkinsonism.

Valente EM, Brancati F, Caputo V, Graham EA, Davis MB, Ferraris A, Breteler MM, Gasser T, Bonifati V, Bentivoglio AR, De Michele G, Dürr A, Cortelli P, Filla A, Meco G, Oostra BA, Brice A, Albanese A, Dallapiccola B, Wood NW; European Consortium on Genetic Susceptibility in Parkinson's Disease.

Neurol Sci. 2002 Sep;23 Suppl 2:S117-8.

PMID:
12548371
[PubMed - indexed for MEDLINE]
6.

Exclusion of the Nurr1 gene in autosomal recessive Parkinson's disease.

Rawal N, Periquet M, Dürr A, de Michele G, Bonifati V, Teive HA, Raskin S, Guimaraes J, Agid Y, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.

J Neurol. 2002 Aug;249(8):1127-9. No abstract available.

PMID:
12420720
[PubMed - indexed for MEDLINE]
7.

PARK6-linked parkinsonism occurs in several European families.

Valente EM, Brancati F, Ferraris A, Graham EA, Davis MB, Breteler MM, Gasser T, Bonifati V, Bentivoglio AR, De Michele G, Dürr A, Cortelli P, Wassilowsky D, Harhangi BS, Rawal N, Caputo V, Filla A, Meco G, Oostra BA, Brice A, Albanese A, Dallapiccola B, Wood NW; European Consortium on Genetic Susceptibility in Parkinson's Disease.

Ann Neurol. 2002 Jan;51(1):14-8.

PMID:
11782979
[PubMed - indexed for MEDLINE]
8.

Association between early-onset Parkinson's disease and mutations in the parkin gene.

Lücking CB, Dürr A, Bonifati V, Vaughan J, De Michele G, Gasser T, Harhangi BS, Meco G, Denèfle P, Wood NW, Agid Y, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.

N Engl J Med. 2000 May 25;342(21):1560-7.

PMID:
10824074
[PubMed - indexed for MEDLINE]
Free Article

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