Lentivirus < Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 < Leukocytes, Mononuclear

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List of bibliographic references

Number of relevant bibliographic references: 26.
[0-20] [0 - 20][0 - 26][20-25][20-40]

Ident.	Authors (with country if any)	Title
000194 (2016)	Massiva Sayad ; Mohamed Zouambia ; Malika Chaouch ; Farida Ferrat ; Mustapha Nebbal ; Mohamed Bendini ; Suzanne Lesage ; Alexis Brice ; Mohamed Brahim Errahmani ; Boualem Asselah	Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.
000216 (2016)	Jean-Marc Taymans ; Elisa Greggio	LRRK2 Kinase Inhibition as a Therapeutic Strategy for Parkinson's Disease, Where Do We Stand?
000265 (2015)	Mickael Ehrminger ; Smaranda Leu-Semenescu ; Florence Cormier ; Jean-Christophe Corvol ; Marie Vidailhet ; Eden Debellemaniere ; Alexis Brice ; Isabelle Arnulf	Sleep aspects on video-polysomnography in LRRK2 mutation carriers.
000333 (2015)	Nadya Pyatigorskaya ; Michael Sharman ; Jean-Christophe Corvol ; Romain Valabregue ; Lydia Yahia-Cherif ; Fabrice Poupon ; Florence Cormier-Dequaire ; Hartwig Siebner ; Stephan Klebe ; Marie Vidailhet ; Alexis Brice ; Stephane Lehéricy	High nigral iron deposition in LRRK2 and Parkin mutation carriers using R2* relaxometry.
000439 (2015)	Lorraine V. Kalia ; Anthony E. Lang ; Lili-Naz Hazrati ; Shinsuke Fujioka ; Zbigniew K. Wszolek ; Dennis W. Dickson ; Owen A. Ross ; Vivianna M. Van Deerlin ; John Q. Trojanowski ; Howard I. Hurtig ; Roy N. Alcalay ; Karen S. Marder ; Lorraine N. Clark ; Carles Gaig ; Eduardo Tolosa ; Javier Ruiz-Martínez ; Jose F. Marti-Masso ; Isidre Ferrer ; Adolfo L Pez De Munain ; Samuel M. Goldman ; Birgitt Schüle ; J William Langston ; Jan O. Aasly ; Maria T. Giordana ; Vincenzo Bonifati ; Andreas Puschmann ; Margherita Canesi ; Gianni Pezzoli ; Andre Maues De Paula ; Kazuko Hasegawa ; Charles Duyckaerts ; Alexis Brice ; A Jon Stoessl ; Connie Marras	Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease.
000528 (2014)	Roy N. Alcalay ; Jan Aasly ; Daniela Berg ; Susan Bressman ; Alexis Brice ; Kathrin Brockmann ; Piu Chan ; Lorraine Clark ; Florence Cormier ; Jean-Christophe Corvol ; Alexandra Durr ; Maurizio Facheris ; Matthew Farrer ; Tatiana M. Foroud ; Thomas Gasser ; Nir Giladi ; Cheryl Halter ; Anthony Lang ; J William Langston ; Connie Marras ; Jose-Felix Marti-Masso ; Javier Ruiz Martinez ; Helen Mejia-Santana ; Anat Mirelman ; Claustre Pont-Sunyer ; Avi Orr-Urtreger ; Deborah Raymond ; Rachel Saunders-Pullman ; Birgitt Schüle ; Caroline Tanner ; Eduardo Tolosa ; Alison Urkowitz ; Dolores Vilas ; Adina Wise ; Karen Marder	Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants.
000608 (2014)	Eugénie Mutez ; Aurore Nkiliza ; Karim Belarbi ; Amélie De Broucker ; Christel Vanbesien-Mailliot ; Séverine Bleuse ; Aurélie Duflot ; Thomas Comptdaer ; Pierre Semaille ; Renaud Blervaque ; David Hot ; Frederic Leprêtre ; Martin Figeac ; Alain Destée ; Marie-Christine Chartier-Harlin	Involvement of the immune system, endocytosis and EIF2 signaling in both genetically determined and sporadic forms of Parkinson's disease.
000730 (2013)	Benjamin Dehay ; Marta Martinez-Vicente ; Guy A. Caldwell ; Kim A. Caldwell ; Zhenyue Yue ; Mark R. Cookson ; Christine Klein ; Miquel Vila ; Erwan Bezard	Lysosomal impairment in Parkinson's disease.
000798 (2013)	Erwan Bezard ; Zhenyu Yue ; Deniz Kirik ; Maria Grazia Spillantini	Animal models of Parkinson's disease: limits and relevance to neuroprotection studies.
000946 (2011)	Olga Corti ; Suzanne Lesage ; Alexis Brice	What genetics tells us about the causes and mechanisms of Parkinson's disease.
000965 (2011)	Cristine Alves Da Costa ; Frédéric Checler	Apoptosis in Parkinson's disease: is p53 the missing link between genetic and sporadic Parkinsonism?
000A08 (2011)	S. Lesage ; C. Condroyer ; N. Hecham ; M. Anheim ; S. Belarbi ; E. Lohman ; F. Viallet ; P. Pollak ; M. Abada ; A. Dürr ; M. Tazir ; A. Brice	Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa.
000A45 (2010)	L. Defebvre	[Parkinson's disease: Role of genetic and environment factors. Involvement in everyday clinical practice].
000A55 (2010)	A R Troiano ; A. Elbaz ; E. Lohmann ; S. Belarbi ; M. Vidailhet ; A-M Bonnet ; S. Lesage ; P. Pollak ; C. Cazeneuve ; M. Borg ; J. Feingold ; A. Dürr ; M. Tazir ; A. Brice	Low disease risk in relatives of north african lrrk2 Parkinson disease patients.
000A64 (2010)	Jérémie Vitte ; Sabine Traver ; André Maués De Paula ; Suzanne Lesage ; Giorgio Rovelli ; Olga Corti ; Charles Duyckaerts ; Alexis Brice	Leucine-rich repeat kinase 2 is associated with the endoplasmic reticulum in dopaminergic neurons and accumulates in the core of Lewy bodies in Parkinson disease.
000A86 (2010)	Suzanne Lesage ; Etienne Patin ; Christel Condroyer ; Anne-Louise Leutenegger ; Ebba Lohmann ; Nir Giladi ; Anat Bar-Shira ; Soraya Belarbi ; Nassima Hecham ; Pierre Pollak ; Anne-Marie Ouvrard-Hernandez ; Soraya Bardien ; Jonathan Carr ; Traki Benhassine ; Hiroyuki Tomiyama ; Caroline Pirkevi ; Tarik Hamadouche ; Cécile Cazeneuve ; A Nazli Basak ; Nobutaka Hattori ; Alexandra Dürr ; Meriem Tazir ; Avi Orr-Urtreger ; Lluis Quintana-Murci ; Alexis Brice	Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.
000B94 (2009)	Ebba Lohmann ; Laurence Leclere ; Francesca De Anna ; Suzanne Lesage ; Bruno Dubois ; Yves Agid ; Alexandra Dürr ; Alexis Brice	A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations.
000B97 (2009)	Suzanne Lesage ; Alexis Brice	Parkinson's disease: from monogenic forms to genetic susceptibility factors.
000C05 (2009)	A. Destée ; E. Mutez ; A. Kreisler ; C. Vanbesien-Maillot ; M C Chartier-Harlin	[Parkinson disease: genetics and neuronal death].
000C48 (2008)	S. Lesage ; S. Belarbi ; A. Troiano ; C. Condroyer ; N. Hecham ; P. Pollak ; E. Lohman ; T. Benhassine ; F. Ysmail-Dahlouk ; A. Dürr ; M. Tazir ; A. Brice	Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?
000E00 (2007)	Suzanne Lesage ; Sabine Janin ; Ebba Lohmann ; Anne-Louise Leutenegger ; Laurence Leclere ; François Viallet ; Pierre Pollak ; Franck Durif ; Stéphane Thobois ; Valérie Layet ; Marie Vidailhet ; Yves Agid ; Alexandra Dürr ; Alexis Brice ; Anne-Marie Bonnet ; Michel Borg ; Emmanuel Broussolle ; Philippe Damier ; Alain Destée ; Maria Martinez ; Christiane Penet ; Olivier Rasco ; François Tison ; Christine Tranchan ; Marc Vérin	LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans.

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