William Camu

William Camu

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An Update on Vitamin D and Disease Activity in Multiple Sclerosis.

CNS Drugs 2019 Nov 4. Epub 2019 Nov 4.

Department of Neurology, Akershus University Hospital, Box 1000, 1478, Lørenskog, Norway.

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http://dx.doi.org/10.1007/s40263-019-00674-8DOI Listing
November 2019

Theme 4 In vivo experimental models.

Amyotroph Lateral Scler Frontotemporal Degener 2019 Nov;20(sup1):160-187

Laboratoire de Biochimie et Biologie Moléculaire, CHU Nîmes et Université de Montpellier, Nimes, France.

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http://dx.doi.org/10.1080/21678421.2019.1646992DOI Listing
November 2019

Cholecalciferol in relapsing-remitting MS: A randomized clinical trial (CHOLINE).

Neurol Neuroimmunol Neuroinflamm 2019 Sep 6;6(5). Epub 2019 Aug 6.

From CHU Gui de Chauliac (W.C.) and Institut de Génomique Fonctionnelle (E.T.), Université de Montpellier, France; Faculty of Economics (P.L.), UCL Mons, Louvain, Belgium; Faculty of Medicine (P.L.), the University of Melbourne, Australia; CHU Pitié Salpêtrière (C.P.-D.), Paris; GHICL St Vincent de Paul (P.H.), Lille; Merck (A.B., A.-S.J.-D., M.P.), Lyon; CHU Caremeau (E.T.), Nîmes; and CHU Necker (J.C.S.), Paris, France.

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http://dx.doi.org/10.1212/NXI.0000000000000597DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6705622PMC
September 2019

Regulation of Brain Cholesterol: What Role Do Liver X Receptors Play in Neurodegenerative Diseases?

Int J Mol Sci 2019 Aug 8;20(16). Epub 2019 Aug 8.

Motoneuron Disease: Pathophysiology and Therapy, The Neuroscience Institute of Montpellier, University of Montpellier, Montpellier, Laboratoire de Biochimie et Biologie Moléculaire, Nimes University Hospital, 30029 Nîmes, France.

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https://www.mdpi.com/1422-0067/20/16/3858
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http://dx.doi.org/10.3390/ijms20163858DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720493PMC
August 2019

Phenotypic and genotypic studies of ALS cases in ALS-SMA families.

Amyotroph Lateral Scler Frontotemporal Degener 2018 08 1;19(5-6):432-437. Epub 2018 Mar 1.

k Clinique du Motoneurone, Explorations neurologiques, CHU Gui de Chauliac , Université de Montpellier , Montpellier , France.

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http://dx.doi.org/10.1080/21678421.2018.1440406DOI Listing
August 2018

Liver X Receptor Genes Variants Modulate ALS Phenotype.

Mol Neurobiol 2018 03 27;55(3):1959-1965. Epub 2017 Feb 27.

INSERM UMR1051, Institut des Neurosciences de Montpellier, Hôpital Saint Eloi, Montpellier, France.

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http://dx.doi.org/10.1007/s12035-017-0453-2DOI Listing
March 2018

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

Authors:
Aude Nicolas Kevin P Kenna Alan E Renton Nicola Ticozzi Faraz Faghri Ruth Chia Janice A Dominov Brendan J Kenna Mike A Nalls Pamela Keagle Alberto M Rivera Wouter van Rheenen Natalie A Murphy Joke J F A van Vugt Joshua T Geiger Rick A Van der Spek Hannah A Pliner Shankaracharya Bradley N Smith Giuseppe Marangi Simon D Topp Yevgeniya Abramzon Athina Soragia Gkazi John D Eicher Aoife Kenna Gabriele Mora Andrea Calvo Letizia Mazzini Nilo Riva Jessica Mandrioli Claudia Caponnetto Stefania Battistini Paolo Volanti Vincenzo La Bella Francesca L Conforti Giuseppe Borghero Sonia Messina Isabella L Simone Francesca Trojsi Fabrizio Salvi Francesco O Logullo Sandra D'Alfonso Lucia Corrado Margherita Capasso Luigi Ferrucci Cristiane de Araujo Martins Moreno Sitharthan Kamalakaran David B Goldstein Aaron D Gitler Tim Harris Richard M Myers Hemali Phatnani Rajeeva Lochan Musunuri Uday Shankar Evani Avinash Abhyankar Michael C Zody Julia Kaye Steven Finkbeiner Stacia K Wyman Alex LeNail Leandro Lima Ernest Fraenkel Clive N Svendsen Leslie M Thompson Jennifer E Van Eyk James D Berry Timothy M Miller Stephen J Kolb Merit Cudkowicz Emily Baxi Michael Benatar J Paul Taylor Evadnie Rampersaud Gang Wu Joanne Wuu Giuseppe Lauria Federico Verde Isabella Fogh Cinzia Tiloca Giacomo P Comi Gianni Sorarù Cristina Cereda Philippe Corcia Hannu Laaksovirta Liisa Myllykangas Lilja Jansson Miko Valori John Ealing Hisham Hamdalla Sara Rollinson Stuart Pickering-Brown Richard W Orrell Katie C Sidle Andrea Malaspina John Hardy Andrew B Singleton Janel O Johnson Sampath Arepalli Peter C Sapp Diane McKenna-Yasek Meraida Polak Seneshaw Asress Safa Al-Sarraj Andrew King Claire Troakes Caroline Vance Jacqueline de Belleroche Frank Baas Anneloor L M A Ten Asbroek José Luis Muñoz-Blanco Dena G Hernandez Jinhui Ding J Raphael Gibbs Sonja W Scholz Mary Kay Floeter Roy H Campbell Francesco Landi Robert Bowser Stefan M Pulst John M Ravits Daniel J L MacGowan Janine Kirby Erik P Pioro Roger Pamphlett James Broach Glenn Gerhard Travis L Dunckley Christopher B Brady Neil W Kowall Juan C Troncoso Isabelle Le Ber Kevin Mouzat Serge Lumbroso Terry D Heiman-Patterson Freya Kamel Ludo Van Den Bosch Robert H Baloh Tim M Strom Thomas Meitinger Aleksey Shatunov Kristel R Van Eijk Mamede de Carvalho Maarten Kooyman Bas Middelkoop Matthieu Moisse Russell L McLaughlin Michael A Van Es Markus Weber Kevin B Boylan Marka Van Blitterswijk Rosa Rademakers Karen E Morrison A Nazli Basak Jesús S Mora Vivian E Drory Pamela J Shaw Martin R Turner Kevin Talbot Orla Hardiman Kelly L Williams Jennifer A Fifita Garth A Nicholson Ian P Blair Guy A Rouleau Jesús Esteban-Pérez Alberto García-Redondo Ammar Al-Chalabi Ekaterina Rogaeva Lorne Zinman Lyle W Ostrow Nicholas J Maragakis Jeffrey D Rothstein Zachary Simmons Johnathan Cooper-Knock Alexis Brice Stephen A Goutman Eva L Feldman Summer B Gibson Franco Taroni Antonia Ratti Cinzia Gellera Philip Van Damme Wim Robberecht Pietro Fratta Mario Sabatelli Christian Lunetta Albert C Ludolph Peter M Andersen Jochen H Weishaupt William Camu John Q Trojanowski Vivianna M Van Deerlin Robert H Brown Leonard H van den Berg Jan H Veldink Matthew B Harms Jonathan D Glass David J Stone Pentti Tienari Vincenzo Silani Adriano Chiò Christopher E Shaw Bryan J Traynor John E Landers

Neuron 2018 03;97(6):1268-1283.e6

Department of Neurology, University of Massachusetts Medical School, Worcester, MA 01605, USA. Electronic address:

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http://dx.doi.org/10.1016/j.neuron.2018.02.027DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867896PMC
March 2018

Teriflunomide-induced psoriasiform changes of fingernails: a new example of paradoxical side effect?

Int J Dermatol 2017 12 7;56(12):1479-1481. Epub 2017 Sep 7.

Department of Neurology, University of Montpellier, Montpellier, France.

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http://dx.doi.org/10.1111/ijd.13742DOI Listing
December 2017

KCC3 loss-of-function contributes to Andermann syndrome by inducing activity-dependent neuromuscular junction defects.

Neurobiol Dis 2017 Oct 21;106:35-48. Epub 2017 Jun 21.

The Institute for Neurosciences of Montpellier, Inserm UMR1051, Saint Eloi Hospital, Montpellier, France; Université Montpellier 1 & 2, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.nbd.2017.06.013DOI Listing
October 2017

The Use of Peripherally Inserted Central Catheter in Amyotrophic Lateral Sclerosis Patients at a Later Stage.

Eur Neurol 2017 16;77(1-2):87-90. Epub 2016 Dec 16.

Clinique du Motoneurone, CHU Gui de Chauliac, Montpellier, France.

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http://dx.doi.org/10.1159/000454858DOI Listing
September 2017

Slowly progressive motor neuron disease with multi-system involvement related to p.E121G SOD1 mutation.

Amyotroph Lateral Scler Frontotemporal Degener 2017 05 28;18(3-4):296-297. Epub 2016 Nov 28.

a Department of Neurology , CHU Montpellier, Hopital Guy de Chauliac , 80 avenue Augustin Fliche , 34295 Montpellier Cedex 5 , France and.

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http://dx.doi.org/10.1080/21678421.2016.1255756DOI Listing
May 2017

CD62L test at 2 years of natalizumab predicts progressive multifocal leukoencephalopathy.

Neurology 2016 12 4;87(23):2491-2494. Epub 2016 Nov 4.

From the CHU Toulouse Purpan (B.P., F.B., D.B., D.A.-P., D.B.), Pôle Neurosciences; INSERM U1043-CNRS UMR 5282 (B.P., F.B., D.B.), Université Toulouse III, Centre de Physiopathologie Toulouse Purpan, France; University of Münster (N.S., T.S.-H., H.W.), Germany; University of Lille (O.O., H.Z., P.V.); Hôpital Civil (J.-C. Ongagna, J.d.S.), Strasbourg; CHU Pellegrin (B.B., J.-C. Ouallet), Bordeaux; CHU Nancy (M.D., S.P.); CHU Caen (G.D., N.D.); CH St Vincent (P.H.), GHICL, Lille; CHU Reims (A.T.); CHU Montpellier (P.L.); CHU Nîmes (G.C., W.C., O.C.); CHRU Clermont Ferrand (P.C.); CHU Besançon (E.B.); Aix Marseille University (J.P., A.R.), APHM, CHU Timone, Marseille; CHU Nantes (D.L., S.W.); CHU Grenoble (E.T.); CHU Dijon (T.M., A.F.); CHU Lyon (S.V.), Bron; Hôpital de la Salpêtrière (C.P.), Paris, France; Centre d'Esclerosi Múltiple de Catalunya (CEMCAT) (M.C.), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Spain; and CHU Nice (C.L.-F.), France.

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http://dx.doi.org/10.1212/WNL.0000000000003401DOI Listing
December 2016

Liver X receptors: from cholesterol regulation to neuroprotection-a new barrier against neurodegeneration in amyotrophic lateral sclerosis?

Cell Mol Life Sci 2016 10 10;73(20):3801-8. Epub 2016 Aug 10.

Department of Biochemistry and Molecular Biology, Nîmes University Hospital, Nîmes, France.

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http://dx.doi.org/10.1007/s00018-016-2330-yDOI Listing
October 2016

Dietary BMAA exposure in an amyotrophic lateral sclerosis cluster from southern France.

PLoS One 2013 13;8(12):e83406. Epub 2013 Dec 13.

Amyotrophic Lateral Sclerosis Center, Centre Hospitalier Universitaire Gui de Chauliac and Institut National de la Santé et de la Recherche Médicale U1051, Montpellier University 1, Montpellier, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0083406PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3862759PMC
September 2014

Peripheral myelin protein 22 gene duplication with atypical presentations: a new example of the wide spectrum of Charcot-Marie-Tooth 1A disease.

Neuromuscul Disord 2014 Jun 13;24(6):524-8. Epub 2014 Apr 13.

Centre de référence «neuropathies périphériques rares», service et laboratoire de Neurologie, CHU Limoges, France.

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http://dx.doi.org/10.1016/j.nmd.2014.03.014DOI Listing
June 2014

Vitamin D confers protection to motoneurons and is a prognostic factor of amyotrophic lateral sclerosis.

Neurobiol Aging 2014 May 13;35(5):1198-205. Epub 2013 Nov 13.

The Neuroscience Institute of Montpellier, Inserm UMR1051, Saint Eloi Hospital, Montpellier, France.

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.11.005DOI Listing
May 2014

[Genetics of amyotrophic lateral sclerosis].

Presse Med 2014 May 2;43(5):555-62. Epub 2014 Apr 2.

CHU Hôpital Gui-de-Chauliac, Centre SLA, université Montpellier I, Inserm 1051, 34295 Montpellier cedex 5, France.

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http://dx.doi.org/10.1016/j.lpm.2014.01.012DOI Listing
May 2014

[Environmental factors in ALS].

Presse Med 2014 May 2;43(5):549-54. Epub 2014 Apr 2.

Hôpital Gui-de-Chauliac, service de neurologie, clinique du motoneurone, Inserm 1051, 34925 Montpellier cedex 5, France. Electronic address:

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http://dx.doi.org/10.1016/j.lpm.2014.02.012DOI Listing
May 2014

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.

Authors:
Ashley H Beecham Nikolaos A Patsopoulos Dionysia K Xifara Mary F Davis Anu Kemppinen Chris Cotsapas Tejas S Shah Chris Spencer David Booth An Goris Annette Oturai Janna Saarela Bertrand Fontaine Bernhard Hemmer Claes Martin Frauke Zipp Sandra D'Alfonso Filippo Martinelli-Boneschi Bruce Taylor Hanne F Harbo Ingrid Kockum Jan Hillert Tomas Olsson Maria Ban Jorge R Oksenberg Rogier Hintzen Lisa F Barcellos Cristina Agliardi Lars Alfredsson Mehdi Alizadeh Carl Anderson Robert Andrews Helle Bach Søndergaard Amie Baker Gavin Band Sergio E Baranzini Nadia Barizzone Jeffrey Barrett Céline Bellenguez Laura Bergamaschi Luisa Bernardinelli Achim Berthele Viola Biberacher Thomas M C Binder Hannah Blackburn Izaura L Bomfim Paola Brambilla Simon Broadley Bruno Brochet Lou Brundin Dorothea Buck Helmut Butzkueven Stacy J Caillier William Camu Wassila Carpentier Paola Cavalla Elisabeth G Celius Irène Coman Giancarlo Comi Lucia Corrado Leentje Cosemans Isabelle Cournu-Rebeix Bruce A C Cree Daniele Cusi Vincent Damotte Gilles Defer Silvia R Delgado Panos Deloukas Alessia di Sapio Alexander T Dilthey Peter Donnelly Bénédicte Dubois Martin Duddy Sarah Edkins Irina Elovaara Federica Esposito Nikos Evangelou Barnaby Fiddes Judith Field Andre Franke Colin Freeman Irene Y Frohlich Daniela Galimberti Christian Gieger Pierre-Antoine Gourraud Christiane Graetz Andrew Graham Verena Grummel Clara Guaschino Athena Hadjixenofontos Hakon Hakonarson Christopher Halfpenny Gillian Hall Per Hall Anders Hamsten James Harley Timothy Harrower Clive Hawkins Garrett Hellenthal Charles Hillier Jeremy Hobart Muni Hoshi Sarah E Hunt Maja Jagodic Ilijas Jelčić Angela Jochim Brian Kendall Allan Kermode Trevor Kilpatrick Keijo Koivisto Ioanna Konidari Thomas Korn Helena Kronsbein Cordelia Langford Malin Larsson Mark Lathrop Christine Lebrun-Frenay Jeannette Lechner-Scott Michelle H Lee Maurizio A Leone Virpi Leppä Giuseppe Liberatore Benedicte A Lie Christina M Lill Magdalena Lindén Jenny Link Felix Luessi Jan Lycke Fabio Macciardi Satu Männistö Clara P Manrique Roland Martin Vittorio Martinelli Deborah Mason Gordon Mazibrada Cristin McCabe Inger-Lise Mero Julia Mescheriakova Loukas Moutsianas Kjell-Morten Myhr Guy Nagels Richard Nicholas Petra Nilsson Fredrik Piehl Matti Pirinen Siân E Price Hong Quach Mauri Reunanen Wim Robberecht Neil P Robertson Mariaemma Rodegher David Rog Marco Salvetti Nathalie C Schnetz-Boutaud Finn Sellebjerg Rebecca C Selter Catherine Schaefer Sandip Shaunak Ling Shen Simon Shields Volker Siffrin Mark Slee Per Soelberg Sorensen Melissa Sorosina Mireia Sospedra Anne Spurkland Amy Strange Emilie Sundqvist Vincent Thijs John Thorpe Anna Ticca Pentti Tienari Cornelia van Duijn Elizabeth M Visser Steve Vucic Helga Westerlind James S Wiley Alastair Wilkins James F Wilson Juliane Winkelmann John Zajicek Eva Zindler Jonathan L Haines Margaret A Pericak-Vance Adrian J Ivinson Graeme Stewart David Hafler Stephen L Hauser Alastair Compston Gil McVean Philip De Jager Stephen J Sawcer Jacob L McCauley

Nat Genet 2013 Nov 29;45(11):1353-60. Epub 2013 Sep 29.

1] John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, USA. [2].

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http://dx.doi.org/10.1038/ng.2770DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3832895PMC
November 2013

Neuroimmunity dynamics and the development of therapeutic strategies for amyotrophic lateral sclerosis.

Front Cell Neurosci 2013 Nov 19;7:214. Epub 2013 Nov 19.

The Neuroscience Institute of Montpellier, INM, INSERM UMR1051, Saint Eloi Hospital Montpellier, France.

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http://dx.doi.org/10.3389/fncel.2013.00214DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833095PMC
November 2013

[Vitamin D and neurology].

Presse Med 2013 Oct 18;42(10):1398-404. Epub 2013 Sep 18.

Hôpital Carémeau, service de neurologie, place du Pr-Debré, 30029 Nîmes cedex 9, France.

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https://linkinghub.elsevier.com/retrieve/pii/S07554982130067
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http://dx.doi.org/10.1016/j.lpm.2013.07.012DOI Listing
October 2013

Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patients.

Neurobiol Aging 2013 Apr 10;34(4):1311.e1-2. Epub 2012 Oct 10.

Centre of Excellence in Neuroscience of Université de Montréal, CHUM Research Center and the Department of Medicine, Université de Montréal, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.09.001DOI Listing
April 2013

Genetic analysis of SIGMAR1 as a cause of familial ALS with dementia.

Eur J Hum Genet 2013 Feb 27;21(2):237-9. Epub 2012 Jun 27.

Centre of Excellence in Neurosciences of Université de Montréal, CHUM Research Center, Montreal, Québec, Canada.

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http://dx.doi.org/10.1038/ejhg.2012.135DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3548267PMC
February 2013

Ipsilateral uveitis and optic neuritis in multiple sclerosis.

Mult Scler Int 2012 19;2012:372361. Epub 2012 Nov 19.

Neurology Department, Hôpital Carémeau, 9 Place Robert Debré, 30029 Nimes Cedex 9, France.

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http://dx.doi.org/10.1155/2012/372361DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507049PMC
December 2012

Lethal multiple sclerosis relapse after natalizumab withdrawal.

Neurology 2012 Nov 24;79(22):2214-6. Epub 2012 Oct 24.

Service d'Anatomopathologie, CHRU de Montpellier, Université Montpellier I, Montpellier, France.

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http://dx.doi.org/10.1212/WNL.0b013e318275979dDOI Listing
November 2012

Subcutaneous IFN-β1a to treat relapsing-remitting multiple sclerosis.

Expert Rev Neurother 2012 Nov 11;12(11):1283-91. Epub 2012 Nov 11.

Service de Neurologie, Hôpital Carémeau, Place du Pr Debré, 30029 Nîmes Cedex 9, France.

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http://dx.doi.org/10.1586/ern.12.122DOI Listing
November 2012

Amyotrophic lateral sclerosis: a hormonal condition?

Amyotroph Lateral Scler 2012 Oct 8;13(6):585-8. Epub 2012 Aug 8.

UMR INSERM U930, Université François Rabelais de Tours, Tours, France.

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http://dx.doi.org/10.3109/17482968.2012.706303DOI Listing
October 2012

UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis.

Neurobiol Aging 2012 Sep 3;33(9):2230.e1-2230.e5. Epub 2012 May 3.

Centre of Excellence in Neuroscience of Université de Montréal (CENUM), CHUM Research Center and the Department of Medicine, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.03.015DOI Listing
September 2012

Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis.

Neurobiol Aging 2012 Aug 22;33(8):1845.e7-9. Epub 2012 Feb 22.

Centre of Excellence in Neurosciences of Université de Montréal, CHUM Research Center, Montreal, QC H2L 4M1, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.01.011DOI Listing
August 2012

Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis.

J Neurol Sci 2012 Jun 14;317(1-2):58-61. Epub 2012 Mar 14.

UMR INSERM U930, Université François-Rabelais, Tours, France; Centre SLA, Service de Neurologie et Neurophysiologie Clinique, CHRU de Tours, France.

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http://dx.doi.org/10.1016/j.jns.2012.02.029DOI Listing
June 2012

Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis.

Neurobiol Aging 2012 Apr 9;33(4):839.e1-3. Epub 2011 Dec 9.

Centre de Recherche de l'Institut du Cerveau et de la Moelle Epinière, INSERM UMR_S975, CNRS UMR7225, Université Pierre et Marie Curie-Paris, Hôpital Pitié-Salpêtrière, Paris, France.

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http://dx.doi.org/10.1016/j.neurobiolaging.2011.11.010DOI Listing
April 2012

Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosis.

Arch Neurol 2011 Jun;68(6):739-42

Centre for Excellence in Neuromics, CHUM Research Center, Université de Montréal, 2099 Alexandre De-Seve St, Montreal, QC H2L 2W5, Canada.

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http://dx.doi.org/10.1001/archneurol.2011.111DOI Listing
June 2011

Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis.

Arch Neurol 2011 May 10;68(5):587-93. Epub 2011 Jan 10.

Centre of Excellence in Neuromics, Centre hospitalier de l'Université de Montréal Research Center, 2099 Alexandre De-Seve St., Montreal, QC, Canada.

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http://dx.doi.org/10.1001/archneurol.2010.351DOI Listing
May 2011

TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1.

Hum Mol Genet 2011 Apr 21;20(7):1400-10. Epub 2011 Jan 21.

Centre d'excellence en neuromique de l'Université de Montréal, Centre de recherche du CHUM, Montréal, QC, Canada.

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http://dx.doi.org/10.1093/hmg/ddr021DOI Listing
April 2011

Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis.

Neurobiol Aging 2011 Mar 11;32(3):555.e13-4. Epub 2010 Nov 11.

Centre of Excellence in Neuromics of Université de Montréal, CHUM Research Center, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2010.10.001DOI Listing
March 2011

Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.

J Hum Genet 2011 Mar 16;56(3):247-9. Epub 2010 Dec 16.

Center of Excellence in Neuromics of Université de Montréal, CHUM Research Center, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1038/jhg.2010.162DOI Listing
March 2011

Screening of OPTN in French familial amyotrophic lateral sclerosis.

Neurobiol Aging 2011 Mar 8;32(3):557.e11-3. Epub 2011 Jan 8.

Centre de Recherche de l'Institut du Cerveau et de la Moelle Epinière, INSERM UMR_S975, CNRS UMR7225, Université Pierre et Marie Curie-Paris 6, Hôpital Pitié-Salpêtrière, Paris, France.

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http://dx.doi.org/10.1016/j.neurobiolaging.2010.11.005DOI Listing
March 2011

Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?

J Neurol Neurosurg Psychiatry 2010 May;81(5):572-7

Department of Clinical Neuroscience, Umeå University, Umeå SE-901 85, Sweden.

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http://dx.doi.org/10.1136/jnnp.2009.192310DOI Listing
May 2010

Association study of the ubiquitin conjugating enzyme gene UBE2H in sporadic ALS.

Amyotroph Lateral Scler 2009 Oct-Dec;10(5-6):432-5

INSERM U930, Université François Rabelais Tours, Montpellier, France.

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http://dx.doi.org/10.3109/17482960802444972DOI Listing
February 2010

The importance of the SMN genes in the genetics of sporadic ALS.

Amyotroph Lateral Scler 2009 Oct-Dec;10(5-6):436-40

ALS Centre, CHU Tours, INSERM, Université François-Rabelais, 2 Boulevard Tonnellé, Tours Cedex 1, France.

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http://dx.doi.org/10.3109/17482960902759162DOI Listing
February 2010

Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.

Proc Natl Acad Sci U S A 2009 Dec 9;106(51):21777-82. Epub 2009 Dec 9.

Centre de Recherche du Centre Hospitalier Universitaire de Québec, Département de psychiatrie et neurosciences, Université Laval, Ste-Foy, QC, Canada G1V 4G2.

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http://dx.doi.org/10.1073/pnas.0902174106DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2799865PMC
December 2009

High metabolic level in patients with familial amyotrophic lateral sclerosis.

Amyotroph Lateral Scler 2009 Apr;10(2):113-7

Department of Neurology and ALS Regional Centre, Hôpital Universitaire Dupuytren, 2 av. Martin-Luther-King, Limoges Cedex, France.

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http://dx.doi.org/10.1080/17482960802295192DOI Listing
April 2009

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.

Arch Neurol 2008 Oct;65(10):1333-6

INSERM U930, Université François Rabelais Tours, CHRU de Tours, Faculté de Médecine, 10 boulevard Tonnellé, BP3223, 37032 Tours CEDEX, France.

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http://dx.doi.org/10.1001/archneur.65.10.1333DOI Listing
October 2008

[Epidemiology and treatment of amyotrophic lateral sclerosis].

Authors:
William Camu

Soins 2008 Jun(726):40-3

Clinique du motoneurone, Hôpital Gui-de-Chauliac, Montpellier.

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June 2008

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.

Nat Genet 2008 May 30;40(5):572-4. Epub 2008 Mar 30.

Center of Excellence in Neuromics, Centre Hospitalier de l'Universite de Montreal, and Department of Medicine, University of Montreal, Montreal, Quebec H2L4MI, Canada.

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http://dx.doi.org/10.1038/ng.132DOI Listing
May 2008

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.

Arch Neurol 2007 Feb;64(2):240-5

Center for the Study of Brain Diseases, University of Montreal, Centre Hospitalier de l'Université de Montréal Research Center, Notre-Dame Hospital, 1560 Sherbrooke Street E., Montreal, Quebec, Canada.

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http://dx.doi.org/10.1001/archneur.64.2.240DOI Listing
February 2007

[Myasthenia gravis in the elderly: diagnosis, comorbidity and course: 45 cases].

Presse Med 2007 Jan 11;36(1 Pt 1):9-14. Epub 2006 Dec 11.

Service de Médecine Interne Gériatrique, Centre Hospitalier Universitaire Caremeau, Nîmes.

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http://dx.doi.org/10.1016/j.lpm.2006.07.003DOI Listing
January 2007

A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis.

J Biol Chem 2004 Oct 17;279(44):45951-6. Epub 2004 Aug 17.

Centre for Research in Neuroscience, McGill University Health Centre, Montreal General Hospital Research Institute, Montreal, Québec H3G 1A4, Canada.

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http://dx.doi.org/10.1074/jbc.M408139200DOI Listing
October 2004

Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis.

Arch Neurol 2003 Dec;60(12):1768-71

Centre for Research in Neuroscience, McGill University, and Montréal General Hospital Research Institute, Montréal, Quebec, Canada.

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http://archneur.jamanetwork.com/article.aspx?doi=10.1001/arc
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http://dx.doi.org/10.1001/archneur.60.12.1768DOI Listing
December 2003

N19S, a new SOD1 mutation in sporadic amyotrophic lateral sclerosis: no evidence for disease causation.

Ann Neurol 2003 Jun;53(6):815-8

Equipe clinique et génétique des maladies du motoneurone U336, Institut de Biologie, Montpellier, France.

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http://dx.doi.org/10.1002/ana.10605DOI Listing
June 2003

A clustering of conjugal amyotrophic lateral sclerosis in southeastern France.

Arch Neurol 2003 Apr;60(4):553-7

Department of Neurology, University Hospital Bretonneau, Tours, France.

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http://dx.doi.org/10.1001/archneur.60.4.553DOI Listing
April 2003

A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.

Am J Hum Genet 2002 Jan 9;70(1):251-6. Epub 2001 Nov 9.

Centre for Research in Neuroscience, McGill University and the Montréal General Hospital Research Institute, Montréal, Canada.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC384894PMC
http://dx.doi.org/10.1086/337945DOI Listing
January 2002