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La maladie de Parkinson en France (serveur d'exploration) - Curation (Ncbi)

Index « Keywords » - entrée « Polymorphism, Genetic »
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Polymers (chemistry) < Polymorphism, Genetic < Polymorphism, Genetic (genetics)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 11.
Ident.Authors (with country if any)Title
000007 (1999) N. Abbas [France] ; C B Lücking ; S. Ricard ; A. Dürr ; V. Bonifati ; G. De Michele ; S. Bouley ; J R Vaughan ; T. Gasser ; R. Marconi ; E. Broussolle ; C. Brefel-Courbon ; B S Harhangi ; B A Oostra ; E. Fabrizio ; G A Böhme ; L. Pradier ; N W Wood ; A. Filla ; G. Meco ; P. Denefle ; Yves Agid [France] ; A. BriceA wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
000169 (2000) C. Mailliot [France] ; T. Bussière ; M. Hamdane ; N. Sergeant ; M L Caillet ; A. Delacourte ; L. BuéePathological tau phenotypes. The weight of mutations, polymorphisms, and differential neuronal vulnerabilities.
000420 (2004) C. Levecque ; A. Elbaz ; J. Clavel ; J. Vidal ; P. Amouyel ; A. Alperovitch ; C. Tzourio ; M. Chartier-HarlinAssociation of polymorphisms in the Tau and Saitohin genes with Parkinson's disease
000424 (2004) Alexis Elbaz ; Clotilde Levecque ; Jacqueline Clavel ; Jean-Sébastien Vidal ; Florence Richard ; Philippe Amouyel ; Annick Alpérovitch ; Marie-Christine Chartier-Harlin ; Christophe TzourioCYP2D6 polymorphism, pesticide exposure, and Parkinson's disease.
000458 (2004) C. Levecque [France] ; A. Destée ; V. Mouroux ; P. Amouyel ; M-C Chartier-HarlinAssessment of Nurr1 nucleotide variations in familial Parkinson's disease.
000A37 (2009) Sarah Vautier [France] ; Christine FernandezABCB1: the role in Parkinson's disease and pharmacokinetics of antiparkinsonian drugs.
000C75 (2011) Jean-Christophe Corvol [France] ; Cécilia Bonnet ; Fanny Charbonnier-Beaupel ; Anne-Marie Bonnet ; Marie-Hélène Fiévet ; Agnès Bellanger ; Emmanuel Roze ; Gayané Meliksetyan ; Mouna Ben Djebara ; Andreas Hartmann ; Lucette Lacomblez ; Cédric Vrignaud ; Noël Zahr ; Yves Agid [France] ; Jean Costentin ; Jean-Sébastien Hulot ; Marie VidailhetThe COMT Val158Met polymorphism affects the response to entacapone in Parkinson's disease: a randomized crossover clinical trial.
001030 (2013) Florence Cormier [France] ; Julia Muellner ; Jean-Christophe CorvolGenetics of impulse control disorders in Parkinson's disease.
001726 (2015) Sonia Lavisse [France] ; Daniel García-Lorenzo [France] ; Marie-Anne Peyronneau [France] ; Benedetta Bodini [Royaume-Uni] ; Claire Thiriez [France] ; Bertrand Kuhnast [France] ; Claude Comtat [France] ; Philippe Remy ; Bruno Stankoff [France] ; Michel Bottlaender [France]Optimized Quantification of Translocator Protein Radioligand ¹⁸F-DPA-714 Uptake in the Brain of Genotyped Healthy Volunteers.
001E66 (1997) V. Planté-Bordeneuve [France] ; D. Taussig ; F. Thomas ; G. Said ; N W Wood ; C D Marsden ; A E HardingEvaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele.
001E81 (1994) R. Bordet [France] ; F. Broly ; A. Destee ; C. LibersaGenetic polymorphism of cytochrome P450 2D6 in idiopathic Parkinson disease and diffuse Lewy body disease.

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