Publications by authors named "Francoise Bouhour"

34Publications

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

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

Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies.

Authors:
Karim Wahbi Rabah Ben Yaou Estelle Gandjbakhch Frédéric Anselme Thomas Gossios Neal K Lakdawala Caroline Stalens Frédéric Sacher Dominique Babuty Jean-Noel Trochu Ghassan Moubarak Kostantinos Savvatis Raphaël Porcher Pascal Laforêt Abdallah Fayssoil Eloi Marijon Tanya Stojkovic Anthony Béhin Sarah Leonard-Louis Guilhem Sole Fabien Labombarda Pascale Richard Corinne Metay Susana Quijano-Roy Ivana Dabaj Didier Klug Marie-Christine Vantyghem Philippe Chevalier Pierre Ambrosi Emmanuelle Salort Nicolas Sadoul Xavier Waintraub Khadija Chikhaoui Philippe Mabo Nicolas Combes Philippe Maury Jean-Marc Sellal Usha B Tedrow Jonathan M Kalman Jitendra Vohra Alexander F A Androulakis Katja Zeppenfeld Tina Thompson Christine Barnerias Henri-Marc Bécane Eric Bieth Franck Boccara Damien Bonnet Françoise Bouhour Stéphane Boulé Anne-Claire Brehin Françoise Chapon Pascal Cintas Jean-Marie Cuisset Jean-Marc Davy Annachiara De Sandre-Giovannoli Florence Demurger Isabelle Desguerre Klaus Dieterich Julien Durigneux Andoni Echaniz-Laguna Romain Eschalier Ana Ferreiro Xavier Ferrer Christine Francannet Mélanie Fradin Bénédicte Gaborit Arnaud Gay Albert Hagège Arnaud Isapof Isabelle Jeru Raul Juntas Morales Emmanuelle Lagrue Nicolas Lamblin Olivier Lascols Vincent Laugel Arnaud Lazarus France Leturcq Nicolas Levy Armelle Magot Véronique Manel Raphaël Martins Michèle Mayer Sandra Mercier Christophe Meune Maud Michaud Marie-Christine Minot-Myhié Antoine Muchir Aleksandra Nadaj-Pakleza Yann Péréon Philippe Petiot Florence Petit Julien Praline Anne Rollin Pascal Sabouraud Catherine Sarret Stéphane Schaeffer Frederic Taithe Céline Tard Vincent Tiffreau Annick Toutain Camille Vatier Ulrike Walther-Louvier Bruno Eymard Philippe Charron Corinne Vigouroux Gisèle Bonne Saurabh Kumar Perry Elliott Denis Duboc

Circulation 2019 07 3;140(4):293-302. Epub 2019 Jun 3.

APHP, Cochin Hospital, Cardiology Department, FILNEMUS, Centre de Référence de Pathologie Neuromusculaire Nord/Est/Ile de France, Paris-Descartes, Sorbonne Paris Cité University (K.W., D.D.).

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http://dx.doi.org/10.1161/CIRCULATIONAHA.118.039410DOI Listing
July 2019

FSHD1 and FSHD2 form a disease continuum.

Neurology 2019 05 12;92(19):e2273-e2285. Epub 2019 Apr 12.

From the Peripheral Nervous System (S.S., M.G., C.C., A.P.), Muscle & ALS Department, Pasteur 2 Hospital, Centre Hospitalier Universitaire de Nice, and Institute for Research on Cancer and Aging of Nice (S.S., C.B., N.L., P.N., G.C.), CNRS, INSERM, Université Côte d'Azur; Department of Genetics and Molecular Biology (A.B.-S., S.R., M.J.), Cochin Hospital, Paris, France; Department of Human Genetics (R.J.L.F.L., S.M.v.d.M.), Leiden University Medical Center, the Netherlands; Rare Neuromuscular Diseases Centre (C.C.), Department of Human Neuroscience, Sapienza University of Rome, Italy; Pathology Department (F.C.), CHRU of Caen, INSERM U1075, University of Caen, Normandy; Myology Institute (T.S., A.B., B.E.), Center of Research in Myology, APHP, Sorbonne Université, UPMC Univ Paris 06, INSERM UMRS974, CNRS FRE3617, Paris; Electromyography and Neuromuscular Department (C.V., F.B., P.P.), Neurologic Hospital, Lyon East Hospital Group, Lyon-Bron, France; Neuromuscular Center, Department of Neuroscience (M.C., E.P.), and Clinical Genetics Unit, Department of Women's and Children's Health (L.S.), University of Padova, Italy; Institut Imagine, Imagine Bioinfomatics Platform (M.B.), Paris Descartes University; Département de Neurologie (A.E.-L.), Hôpitaux Universitaires, Strasbourg; Nord/Est/Ile de France Neuromuscular Center (P.L.), Neurology Department, Raymond Poincaré Teaching Hospital, Garches; INSERM U1179 (P.L.), END-ICAP, Versailles Saint-Quentin-en-Yvelines University, Montigny-le-Bretonneux, France; and IRP Città della Speranza (L.S.), Padova, Italy.

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http://dx.doi.org/10.1212/WNL.0000000000007456DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537132PMC
May 2019

Efficacy and Safety of Octagam® in Patients With Chronic Inflammatory Demyelinating Polyneuropathy.

Neurol Ther 2019 Jun 22;8(1):69-78. Epub 2019 Mar 22.

La Timone University Hospital,, Assistance Publique-Hôpitaux de Marseilles (APHM), 264 rue Saint Pierre, 13005, Marseille, France.

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http://dx.doi.org/10.1007/s40120-019-0132-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534624PMC
June 2019

Late-onset Pompe disease in France: molecular features and epidemiology from a nationwide study.

J Inherit Metab Dis 2018 11 28;41(6):937-946. Epub 2018 Aug 28.

Centre de Référence des Maladies Neuromusculaires Nord-Est-Ile de France, Service de Neurologie, CHU Raymond Poincaré, AP-HP, 104 bd Raymond Poincaré, 92380, Garches, France.

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http://dx.doi.org/10.1007/s10545-018-0243-7DOI Listing
November 2018

Peripheral small fiber dysfunction and neuropathic pain in patients with Morvan syndrome.

Neurology 2015 Dec 23;85(23):2076-8. Epub 2015 Sep 23.

From Explorations Fonctionnelles Neurologiques (C.L., E.O., P.P.), Hôpital de la Croix Rousse, Hospices Civils de Lyon; Service de Neurologie Fonctionnelle et d'Epileptologie (N.A.-O., F.M., L.P.-D.), Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon; French Reference Center for Paraneoplastic Neurological Syndrome (J.-P.C., F.D., J.H.), Hospices Civils de Lyon, Hôpital Neurologique, Bron; Service de Neurologie (J.-P.C.), Hôpital Nord, CHU de Saint Etienne; Lyon Neuroscience Research Center (J.-P.C., F.D., J.H.), INSERM U1028/CNRS UMR 5292, Lyon; Université de Lyon-Université Claude Bernard Lyon 1 (F.M., S.V., F.D., J.H.), Lyon; Service de Neurologie A (S.V.) and Service d'Electroneuromyographie et Pathologies Neuromusculaires (F.B., C.V.), Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon; and Service d'Anatomopathologie (D.M.), Groupement Hospitalier Est, Hospices Civils de Lyon, France.

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http://www.neurology.org/lookup/doi/10.1212/WNL.000000000000
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http://dx.doi.org/10.1212/WNL.0000000000002037DOI Listing
December 2015

Sporadic late-onset nemaline myopathy with MGUS: long-term follow-up after melphalan and SCT.

Neurology 2014 Dec 5;83(23):2133-9. Epub 2014 Nov 5.

From the Departments of Neurology (N.C.V., B.G.v.E.) and Pathology (M.L.), Radboud University Medical Centre, Nijmegen, the Netherlands; Department of Internal Medicine (O.B.), Hôpital Pitié Salpêtrière, UPMC, U974, DHU I2B, Paris, France; Department of Hematology (M.C.M., H.L.), University Medical Center Utrecht, the Netherlands; Department of Pathology (M.L.), Antwerp University Hospital, University of Antwerp, Edegem; Departments of Internal Medicine (W.M.) and Hematology (M.D.), University Hospital Leuven, Belgium; Neurology Service (T.K., J.N.), Lausanne University Hospital CHUV, Lausanne; Department of Medical Oncology (T.P.), University Hospital Bern, Switzerland; Electromyography and Neuromuscular Pathologies Department Lyon Est (F.B.), Bron Hospitals, France; Departments of Pathology (N.R.) and Neurology (B.E.), Hôpital Pitié Salpêtrière, Myology Institute, Paris; Department of Hematology (V.L., P.v.d.B.), Hôpital Pitié Salpêtrière, UPMC Univ Paris 6 GRC 11 GRECHY, Paris, France; Neuromuscular Reference Centre, Department of Neurology (V.L., P.v.d.B.), and Department of Hematology (M.C.V.), Cliniques Universitaires Saint-Luc, University of Louvain, Brussels, Belgium.

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http://dx.doi.org/10.1212/WNL.0000000000001047DOI Listing
December 2014

Atrio-ventricular block requiring pacemaker in patients with late onset Pompe disease.

Neuromuscul Disord 2014 Jul 24;24(7):648-50. Epub 2014 Apr 24.

Neuromuscular Diseases Specialized Center, Archet 1 Hospital, CHU Nice, France.

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http://dx.doi.org/10.1016/j.nmd.2014.04.005DOI Listing
July 2014

Comparison of commercial tests for detecting multiple anti-ganglioside autoantibodies in patients with well-characterized immune-mediated peripheral neuropathies.

Clin Lab 2013 ;59(11-12):1277-87

Hôpitaux de Lyon Laboratoire d'Immunologie, Groupement Hospitalier Lyon Sud 69495 Pierre-Bénite, France.

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http://dx.doi.org/10.7754/clin.lab.2013.121116DOI Listing
February 2014

Absence of airway secretion accumulation predicts tolerance of noninvasive ventilation in subjects with amyotrophic lateral sclerosis.

Respir Care 2013 Sep 15;58(9):1424-32. Epub 2013 Jan 15.

Service d'Electroneuromyographie et Service de Neurologie C, Centre Sclérose Latérale Amyotrophique de Lyon, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Lyon, France.

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http://dx.doi.org/10.4187/respcare.02103DOI Listing
September 2013

Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease.

J Neurol 2012 Jun 17;259(6):1222-6. Epub 2011 Dec 17.

Service de Neurologie Neurovasculaire, Groupe Hospitalier Paris-Saint Joseph, 185 rue Raymond Losserand, 75014 Paris, France.

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http://link.springer.com/content/pdf/10.1007/s00415-011-6340
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http://link.springer.com/10.1007/s00415-011-6340-2
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http://dx.doi.org/10.1007/s00415-011-6340-2DOI Listing
June 2012

Quantitative assessment of skeletal muscle degeneration in patients with myotonic dystrophy type 1 using MRI.

J Magn Reson Imaging 2012 Mar 8;35(3):678-85. Epub 2011 Nov 8.

Université de Lyon, Université Lyon 1, Faculté de médecine Lyon Est, Lyon, France.

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http://doi.wiley.com/10.1002/jmri.22849
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http://dx.doi.org/10.1002/jmri.22849DOI Listing
March 2012

[Identification and characterization of a monoclonal IgM reacting with disialylated gangliosides recognizing the CANOMAD syndrome].

Ann Biol Clin (Paris) 2011 Jul-Aug;69(4):476-80

Centre de biologie et pathologie Est, Service de neurobiologie, Groupement hospitalier Est, Lyon Bron.

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http://dx.doi.org/10.1684/abc.2011.0603DOI Listing
November 2011

[Serum antibody profiles against gangliosides and sulfatide in peripheral neuropathies: evaluation of a new immunoassay].

Ann Biol Clin (Paris) 2010 Nov-Dec;68(6):675-80

Laboratoire d'immunologie, Hôpitaux de Lyon, Centre hospitalier Lyon Sud, Pierre-Bénite.

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http://dx.doi.org/10.1684/abc.2010.0495DOI Listing
December 2011

[Vasculitis multiple mononeuropathies].

Rev Prat 2008 Nov;58(17):1896-9

Service ENMG et pathologies neuromusculaires, hôpital neurologique, groupement hospitalier Est, 69003 Lyon Cedex, France.

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November 2008

Marked improvement of Churg-Strauss vasculitis with intravenous gamma globulins during pregnancy.

Clin Rheumatol 2007 Dec 8;26(12):2149-2151. Epub 2007 May 8.

Service de Medecine Interne, Hôpital Edouard Herriot, 3 Place Arsonval, Lyon, CEDEX 03, 69003, France.

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http://dx.doi.org/10.1007/s10067-007-0628-8DOI Listing
December 2007

[Steinert disease].

Presse Med 2007 Jun 7;36(6 Pt 2):965-71. Epub 2007 Feb 7.

Service d'ENMG et pathologies neuromusculaires, Hôpital neurologique, Bron (69), France.

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http://dx.doi.org/10.1016/j.lpm.2007.01.002DOI Listing
June 2007

Granulomatous myositis: a clinical study of thirteen cases.

Muscle Nerve 2007 Feb;35(2):171-7

Hospices Civils de Lyon, Université Claude Bernard Lyon I, Lyon, France.

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http://dx.doi.org/10.1002/mus.20683DOI Listing
February 2007

[Myasthenia].

Rev Prat 2005 Nov;55(17):1927-32

Service de pathologies neuromusculaires, Hôpital neurologique Pierre Wertheimer, 69394 Lyon.

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November 2005

Ovarian failure related to eukaryotic initiation factor 2B mutations.

Am J Hum Genet 2003 Jun 21;72(6):1544-50. Epub 2003 Apr 21.

INSERM Unité Mixte de Recherche 384, Faculté de Médecine, Clermont-Ferrand, France.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1180314PMC
http://dx.doi.org/10.1086/375404DOI Listing
June 2003