Publications by authors named "Stephanie Millecamps"

47Publications

Clinical and Molecular Landscape of ALS Patients with Mutations: Novel Pathogenic Variants and Novel Phenotypes. A Single ALS Center Study.

Int J Mol Sci 2020 Sep 16;21(18). Epub 2020 Sep 16.

Laboratoire de Biochimie et Biologie Moleculaire, CHU Nimes, Nimes, Motoneuron Disease: Pathophysiology and Therapy, INM, University Montpellier, 30029 Nîmes CEDEX 9, France.

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http://dx.doi.org/10.3390/ijms21186807DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554847PMC
September 2020

Forme juvénile de SLA : l’idée doit FUSer !

Rev Neurol (Paris) 2020 Sep;176S:S39

Neurologie - centre de la sclérose latérale amyotrophique, CHU Gabriel-Montpied, Clermont-Ferrand.

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http://dx.doi.org/10.1016/j.neurol.2020.01.142DOI Listing
September 2020

Spastic paraplegia due to recessive or dominant mutations in can convert to ALS.

Neurol Genet 2019 Dec 13;5(6):e374. Epub 2019 Nov 13.

Institut du Cerveau et de la Moelle épinière (M.-D.-M.A., F.M., E.T., G.S., S.M.), ICM, Inserm U1127, CNRS UMR7225, Sorbonne Université; Département de Neurologie (M.-D.-M.A.), Assistance Publique Hôpitaux de Paris (APHP), Centre de Référence SLA Ile de France, Hôpital de la Pitié-Salpêtrière; Département de Génétique et Cytogénétique (G.B.), Unité Fonctionnelle de neurogénétique moléculaire et cellulaire, APHP, Hôpital Pitié-Salpêtrière, Paris; Centre SLA-MNM (V.D.-B.), Service de Neurologie et Pathologie du Mouvement, Hôpital Roger Salengro, Centre Hospitalier Universitaire (CHU) de Lille; Service de Rééducation Neurologique Cérébrolésion (E.A.), Hôpital Swynghedauw, CHU de Lille; Service de Neurologie (J.-C.A., J.-P.C.), CHU de Saint-Etienne; Service de Neurologie (M.A., G.R., C.T., M.-C.F.), Hôpital de Hautepierre, CHU de Strasbourg; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) (M.A., G.R., C.T.), Université de Strasbourg, Illkirch; Fédération de Médecine Translationnelle de Strasbourg (FMTS) (M.A., G.R., C.T.), Université de Strasbourg; Centre de Référence SLA de Lyon (E.B.), Hôpital Neurologique P. Wertheimer, Hospices Civils de Lyon, CHU de Lyon, Bron; and Ecole Pratique des Hautes Etudes (G.S.), Paris Sciences Lettres Research University, France.

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http://dx.doi.org/10.1212/NXG.0000000000000374DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927358PMC
December 2019

Electrophysiological Characterization of C9ORF72-Associated Amyotrophic Lateral Sclerosis: A Retrospective Study.

Eur Neurol 2019 4;82(4-6):106-112. Epub 2020 Feb 4.

ALS Center, Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer, Service de Neurologie C et Service d'explorations Fonctionnelles Neurologiques, Bron, France.

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http://dx.doi.org/10.1159/000505777DOI Listing
June 2020

Increased prevalence of granulovacuolar degeneration in C9orf72 mutation.

Acta Neuropathol 2019 11 29;138(5):783-793. Epub 2019 May 29.

Raymond Escourolle Neuropathology Department, Groupe Hospitalier Pitié-Salpêtrière Charles Foix, AP-HP, 75651 Cedex 13, Paris, France.

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http://dx.doi.org/10.1007/s00401-019-02028-6DOI Listing
November 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

Adolescence/adult onset MTHFR deficiency may manifest as isolated and treatable distinct neuro-psychiatric syndromes.

Orphanet J Rare Dis 2018 02 1;13(1):29. Epub 2018 Feb 1.

Neurology Department, Reference Center for Lysosomal Diseases, Neurogenetics and Metabolism Unit, AP-HP, GH Pitié-Salpêtrière-Charles Foix, Paris, France.

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https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0
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http://dx.doi.org/10.1186/s13023-018-0767-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796584PMC
February 2018

Amygdala TDP-43 Pathology in Frontotemporal Lobar Degeneration and Motor Neuron Disease.

J Neuropathol Exp Neurol 2017 Sep;76(9):800-812

Service de Neuropathologie, Laboratoire Raymond Escourolle, AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière-Charles Foix, Hôpital de la Pitié-Salpêtrière, Paris, France; Institut du Cerveau et de la Moelle Épinière (ICM), INSERM U1127, CNRS UMR 7225, Sorbonne Universités, Université Pierre et Marie Curie, Univ Paris 06, UPMC-P6 UMR S 1127, Hôpital de la Pitié-Salpêtrière, Paris, France; Département de Neurologie, AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière-Charles Foix, Paris, France; Centre de Référence des Démences Rares, AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière-Charles Foix, Paris, France; Department of Neurology, Tokyo Women's Medical University, Tokyo, Japan; and Laboratory of Structural Neuropathology, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

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http://dx.doi.org/10.1093/jnen/nlx063DOI Listing
September 2017

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.

Authors:
Wouter van Rheenen Aleksey Shatunov Annelot M Dekker Russell L McLaughlin Frank P Diekstra Sara L Pulit Rick A A van der Spek Urmo Võsa Simone de Jong Matthew R Robinson Jian Yang Isabella Fogh Perry Tc van Doormaal Gijs H P Tazelaar Max Koppers Anna M Blokhuis William Sproviero Ashley R Jones Kevin P Kenna Kristel R van Eijk Oliver Harschnitz Raymond D Schellevis William J Brands Jelena Medic Androniki Menelaou Alice Vajda Nicola Ticozzi Kuang Lin Boris Rogelj Katarina Vrabec Metka Ravnik-Glavač Blaž Koritnik Janez Zidar Lea Leonardis Leja Dolenc Grošelj Stéphanie Millecamps François Salachas Vincent Meininger Mamede de Carvalho Susana Pinto Jesus S Mora Ricardo Rojas-García Meraida Polak Siddharthan Chandran Shuna Colville Robert Swingler Karen E Morrison Pamela J Shaw John Hardy Richard W Orrell Alan Pittman Katie Sidle Pietro Fratta Andrea Malaspina Simon Topp Susanne Petri Susanne Abdulla Carsten Drepper Michael Sendtner Thomas Meyer Roel A Ophoff Kim A Staats Martina Wiedau-Pazos Catherine Lomen-Hoerth Vivianna M Van Deerlin John Q Trojanowski Lauren Elman Leo McCluskey A Nazli Basak Ceren Tunca Hamid Hamzeiy Yesim Parman Thomas Meitinger Peter Lichtner Milena Radivojkov-Blagojevic Christian R Andres Cindy Maurel Gilbert Bensimon Bernhard Landwehrmeyer Alexis Brice Christine A M Payan Safaa Saker-Delye Alexandra Dürr Nicholas W Wood Lukas Tittmann Wolfgang Lieb Andre Franke Marcella Rietschel Sven Cichon Markus M Nöthen Philippe Amouyel Christophe Tzourio Jean-François Dartigues Andre G Uitterlinden Fernando Rivadeneira Karol Estrada Albert Hofman Charles Curtis Hylke M Blauw Anneke J van der Kooi Marianne de Visser An Goris Markus Weber Christopher E Shaw Bradley N Smith Orietta Pansarasa Cristina Cereda Roberto Del Bo Giacomo P Comi Sandra D'Alfonso Cinzia Bertolin Gianni Sorarù Letizia Mazzini Viviana Pensato Cinzia Gellera Cinzia Tiloca Antonia Ratti Andrea Calvo Cristina Moglia Maura Brunetti Simona Arcuti Rosa Capozzo Chiara Zecca Christian Lunetta Silvana Penco Nilo Riva Alessandro Padovani Massimiliano Filosto Bernard Muller Robbert Jan Stuit Ian Blair Katharine Zhang Emily P McCann Jennifer A Fifita Garth A Nicholson Dominic B Rowe Roger Pamphlett Matthew C Kiernan Julian Grosskreutz Otto W Witte Thomas Ringer Tino Prell Beatrice Stubendorff Ingo Kurth Christian A Hübner P Nigel Leigh Federico Casale Adriano Chio Ettore Beghi Elisabetta Pupillo Rosanna Tortelli Giancarlo Logroscino John Powell Albert C Ludolph Jochen H Weishaupt Wim Robberecht Philip Van Damme Lude Franke Tune H Pers Robert H Brown Jonathan D Glass John E Landers Orla Hardiman Peter M Andersen Philippe Corcia Patrick Vourc'h Vincenzo Silani Naomi R Wray Peter M Visscher Paul I W de Bakker Michael A van Es R Jeroen Pasterkamp Cathryn M Lewis Gerome Breen Ammar Al-Chalabi Leonard H van den Berg Jan H Veldink

Nat Genet 2016 09 25;48(9):1043-8. Epub 2016 Jul 25.

Department of Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands.

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http://dx.doi.org/10.1038/ng.3622DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556360PMC
September 2016

Defining the spectrum of frontotemporal dementias associated with TARDBP mutations.

Neurol Genet 2016 Jun 26;2(3):e80. Epub 2016 May 26.

Sorbonne Universités (P. Caroppo, A.C., L.G.-N., M.T., S.L., S.M., B.D., A.B., I.L.B.), UPMC Univ Paris 06, UMR S 1127, France; Inserm (P. Caroppo, A.C., L.G.-N., M.T., S.L., S.M., B.D., A.B., I.L.B.), U 1127, Paris, France; CNRS (P. Caroppo, A.C., L.G.-N., S.L., S.M., B.D., A.B., I.L.B.), UMR 7225, Paris, France; ICM (P. Caroppo, A.C., L.G.-N., M.T., S.L., S.M., B.D., A.B., I.L.B.), Paris, France; IRCCS Foundation "Carlo Besta" Neurological Institute, (P. Caroppo), Milan, Italy; Plein Ciel (C.T.-A.), Lyon; EA3082 Labo EMC (C.T.-A.), Université Lyon 2; Service de Neurologie (P. Couratier), Centre Hospitalo-Universitaire Dupuytren, Limoges, France; Department of Neurology (T.H.W., J.C.v.S.), Erasmus Medical Center, Rotterdam, the Netherlands; Centre de Référence des Démences Rares (M.T., F.C., B.D., I.L.B.), AP-HP Hôpitaux Universitaires La Pitié Salpêtrière-Charles Foix, Paris, France; Service de Neurologie (V.G.), Centre Hospitalier de Saint-Brieuc, Saint-Brieuc, France; CMRR (V.G., S.B.), Centre Hospitalo-Universitaire, Rennes, France; Service de Neurologie (S.A.), Centre Hospitalo-Universitaire Pellegrin, Bordeaux, France; Inserm-EPHE-Université de Caen/Basse-Normandie (S.B.), Unité U1077, GIP Cyceron, Caen, France; Neurology/Neuropsychology CMRR Unit (B.L.), CHU Nord, France; Institute of Medical Genetics (S.L.), Catholic University, University Hospital A. Gemelli, Roma, Italy; Unité Fonctionnelle de Neurogénétique Moléculaire et Cellulaire (F.C.), Unité Fonctionnelle de Génétique Clinique (A.B.), Département de Génétique et Cytogénétique, and Département de Neurologie (B.D., A.B., I.L.B.), AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière-Charles Foix, Paris, France.

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http://dx.doi.org/10.1212/NXG.0000000000000080DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4882769PMC
June 2016

Genetic analysis of CHCHD10 in French familial amyotrophic lateral sclerosis patients.

Neurobiol Aging 2016 06 24;42:218.e1-3. Epub 2016 Mar 24.

Institut du Cerveau et de la Moelle épinière (ICM), INSERM U1127, CNRS UMR 7225, Sorbonne Universités, Université Pierre et Marie Curie, Univ Paris 06, UPMC-P6 UMR S 1127, Hôpital de la Pitié-Salpêtrière, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2016.03.022DOI Listing
June 2016

TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts.

Neurobiol Aging 2015 Nov 14;36(11):3116.e5-3116.e8. Epub 2015 Aug 14.

Institut du Cerveau et de la Moelle épinière (ICM), INSERM U1127, CNRS UMR 7225, Sorbonne Universités, Université Pierre et Marie Curie, Univ Paris 06, UPMC-P6 UMR S 1127 Hôpital de la Pitié-Salpêtrière, Paris, France; Département des Maladies du Système Nerveux, AP-HP, Hôpital de la Pitié-Salpêtrière, Paris, France; Département de Génétique et Cytogénétique, Unité Fonctionnelle de Génétique Clinique, AP-HP, Hôpital de la Pitié-Salpêtrière, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2015.08.009DOI Listing
November 2015

System xC- is a mediator of microglial function and its deletion slows symptoms in amyotrophic lateral sclerosis mice.

Brain 2015 Jan 10;138(Pt 1):53-68. Epub 2014 Nov 10.

1 Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, F-75013, Paris, France

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http://dx.doi.org/10.1093/brain/awu312DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4441079PMC
January 2015

Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients.

Neurobiol Aging 2014 Dec 18;35(12):2882.e13-2882.e15. Epub 2014 Jul 18.

Institut du Cerveau et de la Moelle épinière (ICM), CNRS UMR 7225, Inserm U 1127, Sorbonne Universités, Université Pierre et Marie, Univ Paris 06, UPMC-P6 UMR S 1127 - Hôpital Pitié-Salpêtrière, Paris, France; Centre de Référence des Démences Rares, AP-HP, Hôpital de la Pitié-Salpêtrière, Paris, France; Département de Neurologie, AP-HP, Hôpital de la Pitié-Salpêtrière, Paris, France.

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http://dx.doi.org/10.1016/j.neurobiolaging.2014.07.016DOI Listing
December 2014

Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders.

Neurology 2014 Sep 6;83(11):990-5. Epub 2014 Aug 6.

From the Institut du Cerveau et de la Moelle épinière (ICM) (S.L., S.M., G.S., S.R.-P., C.M., A.C., S.D., E.M., P.C., A.B., I.L., E.K.), Sorbonne Université, UPMC Univ Paris 06, UM75, Inserm U1127, Cnrs UMR7225, F-75013, Paris; Ecole Pratique des Hautes Etudes, Laboratoire de Neurogénétique, ICM (G.S.), HéSam Université, GHU Pitié-Salpêtrière, F-75013, Paris; Fédération des Maladies du Système Nerveux, Centre de référence maladies rares SLA (F.S., V.M.), Département de Neuropathologie (D.S.), Department of Neurology (A.-M.B.), Unité Fonctionnelle de neurogénétique moléculaire et cellulaire (E.L.), Département de Génétique et Cytogénétique (A.B.), and Centre de référence Démences Rares (I.L.), AP-HP, Hôpital Pitié-Salpêtrière, F-75013, Paris; Inserm U1079 (D.H.), Rouen; Centre mémoire (F.P.), Université Lille Nord de France, EA1046, CHU, Lille; Neuroépidémiologie Tropicale (P.C.), Université de Limoges INSERM UMR1094, Limoges; Service de Neurologie et Pathologie du Mouvement (V.D.-B.), Hôpital Roger Salengro, CHRU Lille; and Service de neurologie (C.T.), Hôpital de Hautepierre, CHU de Strasbourg, 1 Avenue Molière, Strasbourg, France.

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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000077
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http://dx.doi.org/10.1212/WNL.0000000000000778DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162303PMC
September 2014

Genetic analysis of SS18L1 in French amyotrophic lateral sclerosis.

Neurobiol Aging 2014 May 3;35(5):1213.e9-1213.e12. Epub 2013 Dec 3.

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

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.11.023DOI Listing
May 2014

SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis.

JAMA Neurol 2013 Nov;70(11):1403-10

INSERM, UMR_S975, Centre de Recherche de l'Institut du Cerveau et de la Moelle Epinière, Hôpital de la Salpêtrière, F-75013, Paris, France2Université Pierre Marie Curie-Paris 06, UMR_S975, F-75013, Paris, France3Centre national de la recherche scientifique, UMR 7225, F-75013, Paris, France4AP-HP, Hôpital de la Pitié-Salpêtrière, Centre de Référence des Démences Rares, Paris, France5AP-HP, Hôpital de la Pitié-Salpêtrière, Département des maladies du système nerveux, Paris, France.

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http://archneur.jamanetwork.com/article.aspx?doi=10.1001/jam
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http://dx.doi.org/10.1001/jamaneurol.2013.3849DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199096PMC
November 2013

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology.

Acta Neuropathol 2013 Apr 17;125(4):511-22. Epub 2013 Feb 17.

INSERM UMR_S975, CNRS UMR7225, Université Pierre et Marie Curie-Sorbonne Universités, Hôpital Pitié-Salpêtrière, Paris, France.

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http://link.springer.com/10.1007/s00401-013-1090-0
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http://dx.doi.org/10.1007/s00401-013-1090-0DOI Listing
April 2013

Axonal transport deficits and neurodegenerative diseases.

Nat Rev Neurosci 2013 Mar 30;14(3):161-76. Epub 2013 Jan 30.

Centre de Recherche de l'Institut du Cerveau et de la Moelle Épinière, INSERM UMR_S975, CNRS UMR7225, Université Pierre et Marie Curie, Hôpital de la Pitié-Salpêtrière, 47-83 boulevard de l'Hôpital, 75013 Paris, France.

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http://dx.doi.org/10.1038/nrn3380DOI Listing
March 2013

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

Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family.

Amyotroph Lateral Scler 2012 Jan 30;13(1):132-6. Epub 2011 Aug 30.

Laboratory of Neurogenetics, Department of Neurodegenerative Disorders, Mossakowski Medical Research Centre, Polish Academy of Sciences, Pawińskiego 5, Warsaw, Poland.

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http://dx.doi.org/10.3109/17482968.2011.600316DOI Listing
January 2012

Fronto-temporal lobar degeneration: neuropathology in 60 cases.

J Neural Transm (Vienna) 2011 May 4;118(5):753-64. Epub 2011 May 4.

Centre de Recherche de l'Institut du Cerveau et de la Moelle Epinière, INSERM UMR_S975, CNRS UMR7225, Groupe Hospitalier Pitié-Salpêtrière, AP-HP and UPMC-Sorbonne Universités, Paris, France.

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http://dx.doi.org/10.1007/s00702-011-0649-yDOI Listing
May 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

Abnormal TDP-43 and FUS proteins in muscles of sporadic IBM: similarities in a TARDBP-linked ALS patient.

J Neurol Neurosurg Psychiatry 2011 Dec 18;82(12):1414-6. Epub 2010 Jun 18.

Fédération des Maladies du Système Nerveux, Bât Paul Castaigne, Hôpital Pitié-Salpêtrière, 83 bd de l'Hôpital, 75013 Paris, France;

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http://dx.doi.org/10.1136/jnnp.2010.208868DOI Listing
December 2011

Accumulation of TDP-43 and alpha-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation.

Acta Neuropathol 2009 Oct 16;118(4):561-73. Epub 2009 May 16.

Département de Neuropathologie, UPMC Université Paris 06, AP-HP, Assistance Publique Hôpitaux de Paris, Groupe Hospitalier Pitié-Salpêtrière, INSERM UMR-S 546 (DS) and UMR-S 679 (CD), 47-83 boulevard de l'Hôpital, Paris cedex 13, France.

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http://dx.doi.org/10.1007/s00401-009-0545-9DOI Listing
October 2009

Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish.

Hum Mol Genet 2008 Sep 16;17(17):2691-702. Epub 2008 Jun 16.

Department of Medicine, Center for Excellence in Neuromics, CHUM Research Center, University of Montreal, Montreal, QC, Canada.

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http://dx.doi.org/10.1093/hmg/ddn171DOI Listing
September 2008

[Dysfunction of axonal transport in neuropathies and motor neuron diseases].

Med Sci (Paris) 2008 Jan;24(1):65-71

CNRS UMR7091, Hôpital de la Pitié-Salpêtrière, 83 boulevard de l'Hôpital, Paris, France.

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http://dx.doi.org/10.1051/medsci/200824165DOI Listing
January 2008

Conditional NF-L transgene expression in mice for in vivo analysis of turnover and transport rate of neurofilaments.

J Neurosci 2007 May;27(18):4947-56

Centre de Recherche du Centre Hospitalier de l'Université Laval, Department of Anatomy and Physiology of Laval University, Quebec, Canada.

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http://dx.doi.org/10.1523/JNEUROSCI.5299-06.2007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6672085PMC
May 2007

New movements in neurofilament transport, turnover and disease.

Exp Cell Res 2007 Jun 21;313(10):2110-20. Epub 2007 Mar 21.

Division of Biological Sciences, University of Missouri-Columbia, 1201 East Rollins Street, Columbia, MO 65211, USA.

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http://dx.doi.org/10.1016/j.yexcr.2007.03.011DOI Listing
June 2007

Defective axonal transport of neurofilament proteins in neurons overexpressing peripherin.

J Neurochem 2006 Aug 19;98(3):926-38. Epub 2006 Jun 19.

Research Centre of Centre Hospitalier Universitaire de Québec, Department of Anatomy and Physiology of Laval University, Quebec, Canada.

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http://dx.doi.org/10.1111/j.1471-4159.2006.03932.xDOI Listing
August 2006

1-methyl-4-phenylpyridinium neurotoxicity is attenuated by adenoviral gene transfer of human Cu/Zn superoxide dismutase.

J Neurosci Res 2006 Feb;83(2):233-42

Laboratoire de Genetique Moleculaire de la Neurotransmission et des Processus Neurodegeneratifs (LGN), CNRS UMR 7091, Paris, France.

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http://dx.doi.org/10.1002/jnr.20696DOI Listing
February 2006

Alsin is partially associated with centrosome in human cells.

Biochim Biophys Acta 2005 Aug 19;1745(1):84-100. Epub 2005 Jan 19.

Research Centre of CHUQ, Department of Anatomy and Physiology, Laval University, 2705 Boulevard Laurier, Quebec, QC, Canada G1V 4G2.

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http://dx.doi.org/10.1016/j.bbamcr.2004.12.008DOI Listing
August 2005

Cytoskeletal defects in amyotrophic lateral sclerosis (motor neuron disease).

Novartis Found Symp 2005 ;264:183-92; discussion 192-6, 227-30

Research Center of CHUL and Department ofAnatomy and Physiology of Laval University, 2705 Boulevard Laurier, Quebec, QC, G1V 4G2, Canada.

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April 2005

[35S]Methionine metabolic labeling to study axonal transport of neuronal intermediate filament proteins in vivo.

Methods Cell Biol 2004 ;78:555-71

Research Center of CHUL and Department of Anatomy and Physiology, Laval University, Quebec, G1V 4G2, QC Canada.

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http://dx.doi.org/10.1016/s0091-679x(04)78019-xDOI Listing
March 2005

Neuronal transfer of the human Cu/Zn superoxide dismutase gene increases the resistance of dopaminergic neurons to 6-hydroxydopamine.

J Neurochem 2002 Jul;82(1):101-9

Laboratoire de Génétique Moléculaire de la Neurotransmission et des Processus Neurodégénératifs, CNRS UMR C9923, Hôpital de la Pitié-Salpétrière, 83 boulevard de l'Hôpital, 75013 Paris, France.

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http://dx.doi.org/10.1046/j.1471-4159.2002.00952.xDOI Listing
July 2002

Adenoviral retrograde gene transfer in motoneurons is greatly enhanced by prior intramuscular inoculation with botulinum toxin.

Hum Gene Ther 2002 Jan;13(2):225-32

Laboratoire de Génétique Moléculaire de la Neurotransmission et des Processus Neurodégénératifs, Centre National de la Recherche Scientifique, FRE 2360, Hôpital de la Pitié Salpêtrière, 75013 Paris, France.

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http://dx.doi.org/10.1089/10430340252769752DOI Listing
January 2002