Polymorphisme And NotAnnick Alperovitch

List of bibliographic references

Number of relevant bibliographic references: 13.

Ident.	Authors (with country if any)	Title
000301	Jean-Christophe Corvol [France] ; Cécilia Bonnet [France] ; Fanny Charbonnier-Beaupel [France] ; Anne-Marie Bonnet [France] ; Marie-Hélène Fievet [France] ; Agnès Bellanger [France] ; Emmanuel Roze [France] ; Gayané Meliksetyan [France] ; MOUNA BEN DJEBARA [France] ; Andreas Hartmann [France] ; Lucette Lacomblez [France] ; Cédric Vrignaud [France] ; Noël Zahr [France] ; Yves Agid [France] ; Jean Costentin [France] ; Jean-Sébastien Hulot [France] ; Marie Vidailhet [France]	The COMT Val158Met Polymorphism Affects the Response to Entacapone in Parkinson's Disease: A Randomized Crossover Clinical Trial
000474	Evangelos Evangelou [Grèce, Suisse] ; Demetrius M. Maraganore [États-Unis] ; Grazia Annesi [Italie] ; Laura Brighina [Italie] ; Alexis Brice [France] ; Alexis Elbaz [France] ; Carlo Ferrarese [Italie] ; Georgios M. Hadjigeorgiou [Grèce] ; Rejko Krueger [Grèce] ; Jean-Charles Lambert [France] ; Suzanne Lesage [France] ; Katerina Markopoulou [Grèce] ; George D. Mellick [Australie] ; Bram Meeus [Belgique] ; Nancy L. Pedersen [Suède] ; Aldo Quattrone [Italie] ; Christine Van Broeckhoven [Belgique] ; Manu Sharma [Allemagne] ; Peter A. Silburn [Australie] ; Eng-King Tan [Singapour] ; Karin Wirdefeldt [Suède] ; John P. A. Ioannidis [Grèce]	Non-Replication of Association for Six Polymorphisms From Meta-Analysis of Genome-Wide Association Studies of Parkinson's Disease: Large-Scale Collaborative Study
000713	Agnès Camuzat [France] ; Marc Romana [France] ; Alexandra Dürr [France] ; Josué Feingold [France] ; Alexis Brice [France] ; Merle Ruberg [France] ; Annie Lannuzel [France]	The PSP-Associated MAPT H1 Subhaplotype in Guadeloupean Atypical Parkinsonism
000C69	C. Levecque [France] ; A. Elbaz [France] ; J. Clavel [France] ; J. S. Vidal [France] ; P. Amouyel [France] ; A. Alperovitch [France] ; C. Tzourio [France] ; M. C. Chartier-Harlin [France]	Association of polymorphisms in the Tau and Saitohin genes with Parkinson's disease
000D96	Christoph-Burkhard Lücking [France] ; Véronique Chesneau [France] ; Ebba Lohmann [France] ; Patrice Verpillat [France] ; Cyprien Dulac [France] ; Anne-Marie Bonnet [France] ; Francesca Gasparini [France] ; Yves Agid [France] ; Alexandra Dürr [France] ; Alexis Brice [France]	Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease
000F70	Claire Borie [France] ; Francesca Gasparini [France] ; Patrice Verpillat [France] ; Anne-Marie Bonnet [France] ; Yves Agid [France] ; Gilles Hetet [France] ; Alexis Brice [France] ; Alexandra Dürr [France] ; Bernard Grandchamp [France]	Association study between iron-related genes polymorphisms and Parkinson's disease
001041	C. Levecque [France] ; A. Destee [France] ; V. Mouroux [France] ; E. Becquet [France] ; L. Defebvre [France] ; P. Amouyel [France] ; M.-C. Chartier-Harlin [France]	No genetic association of the Ubiquitin Carboxy-terminal Hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease
001289	G. Mercier [France] ; J. C. Turpin [France] ; G. Lucotte [France]	Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease : no association found
001370	N. Abbas [France] ; C. B. Lücking [France] ; S. Ricard [France] ; A. Dürr [France] ; V. Bonifati [Italie] ; G. De Michele [Italie] ; S. Bouley [France] ; J. R. Vaughan [Royaume-Uni] ; T. Gasser [Allemagne] ; R. Marconi [Italie] ; E. Broussolle [France] ; C. Brefel-Courbon [France] ; B. S. Harhangi [Pays-Bas] ; B. A. Oostra [Pays-Bas] ; E. Fabrizio [Italie] ; G. A. Böhme [France] ; L. Pradier [France] ; N. W. Wood [Royaume-Uni] ; A. Filla [Italie] ; G. Meco [Italie] ; P. Denefle [France] ; Yves Agid [France] ; A. Brice [France]	A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe
001642	G. Lucotte [France] ; J.-C. Turpin [France] ; N. Gerard [France] ; S. Panserat [France] ; R. Krishnamoorthy [France]	Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in families
001646	R. Bordet [France] ; F. Broly [France] ; A. Destee [France] ; C. Libersa [France] ; J. Lafitte [France]	Lack of relation between genetic polymorphism of cytochrome p-450IID6 and sporadic idiopathic Parkinson's disease
001780	J. T. Borlak [France] ; V. Harsany ; H. Schneible ; K. D. Haegele	pNAT and CYP2D6 gene polymorphism in epileptic patients
001802	R. Bordet [France] ; F. Broly [France] ; A. Destee [France] ; C. Libersa [France]	Genetic polymorphism of cytochrome P450 2D6 in idiopathic Parkinson disease and diffuse lewy body disease

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