Genomics < Genotype < Geriatric Assessment

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 39.
[20-40] [0 - 20][0 - 39]

Ident.	Authors (with country if any)	Title
000F44 (2004)	M. Martinez [France] ; A. Brice ; J R Vaughan ; A. Zimprich ; M M B. Breteler ; G. Meco ; A. Filla ; M J Farrer ; C. Bétard ; J. Hardy ; G. De Michele ; V. Bonifati ; B. Oostra ; T. Gasser ; N W Wood ; A. Dürr	Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease.
000F62 (2004)	C. Levecque [France] ; A. Destée ; V. Mouroux ; P. Amouyel ; M-C Chartier-Harlin	Assessment of Nurr1 nucleotide variations in familial Parkinson's disease.
000F85 (2004)	O. Santt [France] ; H. Baranova ; E. Albuisson ; Y-J Bignon ; G. Lucotte	Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's disease.
001038 (2003)	Christoph-Burkhard Lücking [France] ; Véronique Chesneau ; Ebba Lohmann ; Patrice Verpillat ; Cyprien Dulac ; Anne-Marie Bonnet ; Francesca Gasparini ; Yves Agid ; Alexandra Dürr ; Alexis Brice	Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.
001045 (2003)	Ebba Lohmann [France] ; Magali Periquet ; Vincenzo Bonifati ; Nick W. Wood ; Giuseppe De Michele ; Anne-Marie Bonnet ; Valérie Fraix ; Emmanuel Broussolle ; Martin W I M. Horstink ; Marie Vidailhet ; Patrice Verpillat ; Thomas Gasser ; David Nicholl ; Hélio Teive ; Salmo Raskin ; Olivier Rascol ; Alain Destée ; Merle Ruberg ; Francesca Gasparini ; Giuseppe Meco ; Yves Agid ; Alexandra Durr ; Alexis Brice	How much phenotypic variation can be attributed to parkin genotype?
001083 (2003)	Alexis Elbaz [France] ; Clotilde Levecque ; Jacqueline Clavel ; Jean-Sébastien Vidal ; Florence Richard ; Jean-René Corrèze ; Bernard Delemotte ; Philippe Amouyel ; Annick Alpérovitch ; Marie-Christine Chartier-Harlin ; Christophe Tzourio	S18Y polymorphism in the UCH-L1 gene and Parkinson's disease: evidence for an age-dependent relationship.
001143 (2002)	Patrice Verpillat [France] ; Agnès Camuzat ; Didier Hannequin ; Catherine Thomas-Anterion ; Michèle Puel ; Serge Belliard ; Bruno Dubois ; Mira Didic ; Bernard-François Michel ; Lucette Lacomblez ; Olivier Moreaud ; François Sellal ; Véronique Golfier ; Dominique Campion ; Françoise Clerget-Darpoux ; Alexis Brice	Association between the extended tau haplotype and frontotemporal dementia.
001169 (2002)	Nathalie Gérard [France] ; Stéphane Panserat ; Gérard Lucotte	Roles of gender, age at onset and environmental risk in the frequency of CYP2D6-deficient alleles in patients with Parkinson's disease.
001233 (2001)	C. Levecque [France] ; A. Destée ; V. Mouroux ; E. Becquet ; L. Defebvre ; P. Amouyel ; M C Chartier-Harlin	No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease.
001274 (2000)	A. Simon [France] ; C. Savy ; E. Martin-Martinelli ; A. Douhou ; F. Frédéric ; C. Verney ; J. Nguyen-Legros ; R. Raisman-Vozari	Paradoxical increase of tyrosine hydroxylase-immunoreactive retinopetal fibers in the weaver mouse.
001367 (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 ; Y. Agid ; A. Brice	A 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.
001375 (1999)	N. Sabbagh [France] ; A. Brice ; D. Marez ; A. Dürr ; M. Legrand ; J M Lo Guidice ; A. Destée ; Y. Agid ; F. Broly	CYP2D6 polymorphism and Parkinson's disease susceptibility.
001529 (1996)	A. Dürr [France] ; A. Brice	Genetics of movement disorders.
001531 (1996)	G. Lucotte [France] ; J C Turpin ; N. Gérard ; S. Panserat ; R. Krishnamoorthy	Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in families.
001534 (1996)	R. Bordet [France] ; F. Broly ; A. Destée ; C. Libersa ; J J Lafitte	Lack of relation between genetic polymorphism of cytochrome P-450IID6 and sporadic idiopathic Parkinson's disease.
001554 (1996)	L. Buée [France] ; J. Pérez-Tur ; B. Leveugle ; V. Buée-Scherrer ; E J Mufson ; A J Loerzel ; M C Chartier-Harlin ; D P Perl ; A. Delacourte ; P R Hof	Apolipoprotein E in Guamanian amyotrophic lateral sclerosis/parkinsonism-dementia complex: genotype analysis and relationships to neuropathological changes.
001555 (1996)	R. Bordet [France] ; F. Broly ; A. Destée ; C. Libersa	Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.
001620 (1994)	R. Bordet [France] ; F. Broly ; A. Destee ; C. Libersa	Genetic polymorphism of cytochrome P450 2D6 in idiopathic Parkinson disease and diffuse Lewy body disease.
001765 (1991)	H. De Reuse [France] ; A. Danchin	Positive regulation of the pts operon of Escherichia coli: genetic evidence for a signal transduction mechanism.

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