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Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

Publikováno v: Neurobiology of aging (2011).
info:cnr-pdr/source/autori:Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destée A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Gispert S, Hattori N, Jasinska-Myga B, Klein C,/titolo:Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease./doi:/rivista:Neurobiology of aging/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volume

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::4696fa91ed3927ccf489b919483d5604
https://publications.cnr.it/doc/50352

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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study

Publikováno v: Lancet neurology
(2011).
info:cnr-pdr/source/autori:Ross OA, Soto-Ortolaza AI, Heckman MG, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Van Broeckhoven C, Carr J, Chartier-Harlin MC, Dardiotis E, Dickson DW, Diehl NN, Elbaz A, Ferrarese C, Ferraris A, Fiske B, Gibson JM./titolo:Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study./doi:/rivista:Lancet neurology (Print)/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volume

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::d2a4f03984c92a18d6253e09305d4d76
https://publications.cnr.it/doc/50335

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Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease

Autor: Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Dürr A, Eblan MJ, Fahn S, Farrer MJ, Fung HC, Gan-Or Z, Gasser T, Gershoni-Baruch R, Giladi N, Griff

Publikováno v: New England journal of medicine (Online) (2009).
info:cnr-pdr/source/autori:Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Dürr A, Eblan MJ, Fahn S, Farrer MJ, Fung HC, Gan-Or Z, Gasser T, Gershoni-Baruch R, Giladi N, Griff/titolo:Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease./doi:/rivista:New England journal of medicine (Online)/anno:2009/pagina_da:/pagina_a:/intervallo_pagine:/volume

BACKGROUND: Recent studies indicate an increased frequency of mutations in the gene encoding glucocerebrosidase (GBA), a deficiency of which causes Gaucher's disease, among patients with Parkinson's disease. We aimed to ascertain the frequency of GBA

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::6a89dd2c305ef1ae4da7c180d5411a7b
https://publications.cnr.it/doc/50023

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Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease

Publikováno v: 296 (2006): 661–670.
info:cnr-pdr/source/autori:Maraganore DM, de Andrade M, Elbaz A, Farrer MJ, Ioannidis JP, Kruger R, Rocca WA, Schneider NK, Lesnick TG, Lincoln SJ, Hulihan MM, Aasly JO, Ashizawa T, Chartier-Harlin MC, Checkoway H, Ferrarese C, Hadjigeorgiou G, Hattori N, Kawakami H, Lambert JC/titolo:Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease./doi:/rivista:/anno:2006/pagina_da:661/pagina_a:670/intervallo_pagine:661–670/volume:296

CONTEXT: Identification and replication of susceptibility genes for Parkinson disease at the population level have been hampered by small studies with potential biases. Alpha-synuclein (SNCA) has been one of the most promising susceptibility genes, b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::bad7ab230c2d5c16e21b53f0298797eb
http://www.cnr.it/prodotto/i/49983

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