Age Factors < Age of Onset < Aged

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 42.
[0-20] [0 - 20][0 - 42][20-40]

Ident.	Authors (with country if any)	Title
000496 (2014)	Serge Pinto ; Murielle Ferraye ; Robert Espesser ; Valérie Fraix ; Audrey Maillet ; Jennifer Guirchoum ; Deborah Layani-Zemour ; Alain Ghio ; Stéphan Chabardès ; Pierre Pollak ; Bettina Debû	Stimulation of the pedunculopontine nucleus area in Parkinson's disease: effects on speech and intelligibility.
000588 (2014)	L. Daelman ; F. Sedel ; A. Tourbah	Progressive neuropsychiatric manifestations of phenylketonuria in adulthood.
000701 (2013)	Anne Roubergue ; Emmanuel Roze ; Sandrine Vuillaumier-Barrot ; Marie-Joséphine Fontenille ; Aurélie Méneret ; Marie Vidailhet ; Bertrand Fontaine ; Diane Doummar ; Bertrand Philibert ; Florence Riant ; Sophie Nicole	The multiple faces of the ATP1A3-related dystonic movement disorder.
000704 (????)	Stéphan Chabardès ; Mircea Polosan ; Paul Krack ; Julien Bastin ; Alexandre Krainik ; Olivier David ; Thierry Bougerol ; Alim Louis Benabid	Deep brain stimulation for obsessive-compulsive disorder: subthalamic nucleus target.
000728 (2013)	Stephan Klebe ; Jean-Louis Golmard ; Michael A. Nalls ; Mohamad Saad ; Andrew B. Singleton ; Jose M. Bras ; John Hardy ; Javier Simon-Sanchez ; Peter Heutink ; Gregor Kuhlenb Umer ; Rim Charfi ; Christine Klein ; Johann Hagenah ; Thomas Gasser ; Isabel Wurster ; Suzanne Lesage ; Delia Lorenz ; Günther Deuschl ; Franck Durif ; Pierre Pollak ; Philippe Damier ; François Tison ; Alexandra Durr ; Philippe Amouyel ; Jean-Charles Lambert ; Christophe Tzourio ; Cécilia Maubaret ; Fanny Charbonnier-Beaupel ; Khadija Tahiri ; Marie Vidailhet ; Maria Martinez ; Alexis Brice ; Jean-Christophe Corvol	The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism.
000778 (2013)	Kathy Dujardin ; Albert F G. Leentjens ; Carole Langlois ; Anja J H. Moonen ; Annelien A. Duits ; Anne-Sophie Carette ; Alain Duhamel	The spectrum of cognitive disorders in Parkinson's disease: a data-driven approach.
000893 (2012)	N. Carrière ; A. Kreisler ; K. Dujardin ; A. Destée ; L. Defebvre	[Impulse control disorders in Parkinson's disease: A cohort of 35 patients].
000975 (2011)	Alexis Elbaz ; Owen A. Ross ; John P A. Ioannidis ; Alexandra I. Soto-Ortolaza ; Frédéric Moisan ; Jan Aasly ; Grazia Annesi ; Maria Bozi ; Laura Brighina ; Marie-Christine Chartier-Harlin ; Alain Destée ; Carlo Ferrarese ; Alessandro Ferraris ; J Mark Gibson ; Suzana Gispert ; Georgios M. Hadjigeorgiou ; Barbara Jasinska-Myga ; Christine Klein ; Rejko Krüger ; Jean-Charles Lambert ; Katja Lohmann ; Simone Van De Loo ; Marie-Anne Loriot ; Timothy Lynch ; George D. Mellick ; Eugénie Mutez ; Christer Nilsson ; Grzegorz Opala ; Andreas Puschmann ; Aldo Quattrone ; Manu Sharma ; Peter A. Silburn ; Leonidas Stefanis ; Ryan J. Uitti ; Enza Maria Valente ; Carles Vilari O-Güell ; Karin Wirdefeldt ; Zbigniew K. Wszolek ; Georgia Xiromerisiou ; Demetrius M. Maraganore ; Matthew J. Farrer	Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.
000B27 (2010)	Sandrine Greffard ; Marc Verny ; Anne-Marie Bonnet ; Danielle Seilhean ; Jean-Jacques Hauw ; Charles Duyckaerts	A stable proportion of Lewy body bearing neurons in the substantia nigra suggests a model in which the Lewy body causes neuronal death.
000B52 (2009)	F. Torny ; M. Lacoste ; H. Videaud ; M. Chouly ; M-C Parveau ; P. Couratier	[Comparison of quality of life in multiple system atrophy and Parkinson's disease].
000B80 (2009)	Cécile Cazeneuve ; Channkanira Sân ; Salah A. Ibrahim ; Maowia M. Mukhtar ; Musa M. Kheir ; Eric Leguern ; Alexis Brice ; Mustafa A. Salih	A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson's disease.
000C28 (2009)	E. Lohmann ; S. Thobois ; S. Lesage ; E. Broussolle ; S Tezenas Du Montcel ; M-J Ribeiro ; P. Remy ; A. Pelissolo ; B. Dubois ; L. Mallet ; P. Pollak ; Y. Agid ; A. Brice	A multidisciplinary study of patients with early-onset PD with and without parkin mutations.
000D27 (2008)	S. Lesage ; E. Lohmann ; F. Tison ; F. Durif ; A. Dürr ; A. Brice	Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls.
000E14 (2007)	Suzanne Lesage ; Periquet Magali ; Ebba Lohmann ; Lucette Lacomblez ; Helio Teive ; Sabine Janin ; Pierre-Yves Cousin ; Alexandra Dürr ; Alexis Brice	Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism.
000E44 (2006)	Anne-Louise Leutenegger ; Mustafa A M. Salih ; Pablo Ibá Ez ; Maowia M. Mukhtar ; Suzanne Lesage ; Ali Arabi ; Ebba Lohmann ; Alexandra Dürr ; Ammar E M. Ahmed ; Alexis Brice	Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1.
000F52 (2005)	F. Bonneville ; M L Welter ; C. Elie ; S Tezenas Du Montcel ; D. Hasboun ; C. Menuel ; J L Houeto ; A M Bonnet ; V. Mesnage ; B. Pidoux ; S. Navarro ; P. Cornu ; Y. Agid ; D. Dormont	Parkinson disease, brain volumes, and subthalamic nucleus stimulation.
000F69 (2005)	Jean-Philippe Galanaud ; Alexis Elbaz ; Jacqueline Clavel ; Jean-Sébastien Vidal ; Jean-René Corrèze ; Annick Alpérovitch ; Christophe Tzourio	Cigarette smoking and Parkinson's disease: a case-control study in a population characterized by a high prevalence of pesticide exposure.
000F72 (????)	Alexis Brice	How much does dardarin contribute to Parkinson's disease?
000F98 (????)	P. Ibá Ez ; A-M Bonnet ; B. Débarges ; E. Lohmann ; F. Tison ; P. Pollak ; Y. Agid ; A. Dürr ; A. Brice	Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease.
000F99 (????)	Marie-Christine Chartier-Harlin ; Jennifer Kachergus ; Christophe Roumier ; Vincent Mouroux ; Xavier Douay ; Sarah Lincoln ; Clotilde Levecque ; Lydie Larvor ; Joris Andrieux ; Mary Hulihan ; Nawal Waucquier ; Luc Defebvre ; Philippe Amouyel ; Matthew Farrer ; Alain Destée	Alpha-synuclein locus duplication as a cause of familial Parkinson's disease.
001013 (2004)	P. Ibá Ez ; E. Lohmann ; P. Pollak ; F. Durif ; C. Tranchant ; Y. Agid ; A. Dürr ; A. Brice	Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease.

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