Christine Tranchant

Christine Tranchant

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Christine Tranchant

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Atypical Parkinson Syndrome Hiding a Meningioma.

Clin Nucl Med 2019 Sep 12. Epub 2019 Sep 12.

From the Service de Biophysique et Médecine Nucléaire, Hôpitaux Universitaires de Strasbourg.

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http://dx.doi.org/10.1097/RLU.0000000000002767DOI Listing
September 2019

Descriptive analysis of the French NS-Park registry: Towards a nation-wide Parkinson's disease cohort?

Parkinsonism Relat Disord 2019 Jul 25;64:226-234. Epub 2019 Apr 25.

Sorbonne Université, Assistance Publique Hôpitaux de Paris, Institut du Cerveau et de la Moelle épinière, ICM, Inserm U 1127, CNRS UMR 7225, Department of Neurology, Hôpital Pitié-Salpêtrière, F-75013, Paris, France; Center for Interdisciplinary Research in Biology, Collège de France, INSERM U1050, CNRS UMR7241, Labex Memolife, Paris Sciences et Lettres, Paris, France; AP-HP, Department of Neurology, Hôpital Avicenne, Hôpitaux Universitaires de Paris - Seine Saint Denis, Bobigny, France. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2019.04.012DOI Listing
July 2019

Deep brain stimulation does not enhance neuroinflammation in multiple system atrophy.

Neurobiol Dis 2018 10 17;118:155-160. Epub 2018 Jul 17.

Univ. de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France; Centre de Référence Maladie Rare AMS, CHU de Bordeaux, F-33000 Bordeaux, France; Service de Neurologie, CHU de Bordeaux, F-33000 Bordeaux, France. Electronic address:

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http://dx.doi.org/10.1016/j.nbd.2018.07.016DOI Listing
October 2018

Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect.

Orphanet J Rare Dis 2018 10 1;13(1):175. Epub 2018 Oct 1.

Reference Centre for Lysosomal Diseases (CRML), Department of Pediatric Neurology, and Sorbonne Université, GRC n°19, Pathologies Congénitales du Cervelet-LeucoDystrophies, AP-HP, Hôpital Armand Trousseau, F-75012, 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/s13023-018-0913-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167825PMC
October 2018

A recessive ataxia diagnosis algorithm for the next generation sequencing era.

Ann Neurol 2017 Dec 21;82(6):892-899. Epub 2017 Nov 21.

Department of Neurology, Hautepierre Hospital, University Hospitals of Strasbourg, Strasbourg, France.

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http://dx.doi.org/10.1002/ana.25084DOI Listing
December 2017

Ability of pulmonary function decline to predict death in amyotrophic lateral sclerosis patients.

Amyotroph Lateral Scler Frontotemporal Degener 2017 11 20;18(7-8):511-518. Epub 2017 Jul 20.

a Department of Physiology and Pulmonary Function Tests, Chest diseases , University Hospital of Strasbourg and EA 3072, Federation of Translational Medicine, Strasbourg University , Strasbourg Cedex , France.

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http://dx.doi.org/10.1080/21678421.2017.1353097DOI Listing
November 2017

Parkinsonian-Pyramidal syndromes: A systematic review.

Parkinsonism Relat Disord 2017 06 22;39:4-16. Epub 2017 Feb 22.

Service de Neurologie, Hopital de Hautepierre, Strasbourg, France; Fédération de Médecine Translationnelle, Faculté de Médecine, Strasbourg, France.

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http://dx.doi.org/10.1016/j.parkreldis.2017.02.025DOI Listing
June 2017

SCA13 causes dominantly inherited non-progressive myoclonus ataxia.

Parkinsonism Relat Disord 2017 05 11;38:80-84. Epub 2017 Feb 11.

Département de Neurologie, Hôpital de Hautepierre, CHU de Strasbourg, Strasbourg, France; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM-U964/CNRS-UMR7104/Université de Strasbourg, Illkirch, France; Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg, France. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2017.02.012DOI Listing
May 2017

Subacute parkinsonism as a complication of Lyme disease.

J Neurol 2017 May 27;264(5):1015-1019. Epub 2017 Mar 27.

Department of Neurology, CHRU Strasbourg, 1 Avenue Molière, 67098, Strasbourg Cedex, France.

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http://dx.doi.org/10.1007/s00415-017-8472-5DOI Listing
May 2017

[Other causes of parkinsonism].

Presse Med 2017 Mar 23;46(2 Pt 1):210-217. Epub 2017 Jan 23.

Hôpital de Hautepierre, service de neurologie, unité des pathologies du mouvement, 1, avenue Molière, 67000 Strasbourg, France. Electronic address:

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http://dx.doi.org/10.1016/j.lpm.2016.11.008DOI Listing
March 2017

Low cancer prevalence in polyglutamine expansion diseases.

Neurology 2017 Mar 15;88(12):1114-1119. Epub 2017 Feb 15.

From ICM Institut du Cerveau et de la Moelle Épinière (G.C., D.R., A.B., F.M., A.D.), Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127; Sorbonne Universités (A.D., S.T.d.M.), UPMC Univ Paris 06 UMR_S1136; INSERM UMR_S 1136 (A.D., S.T.d.M.), Institut Pierre Louis d'Epidémiologie et de Santé Publique; Institut Curie (M.S.T.), Paris; University Paris Sud 11 (M.S.T.), Orsay; CIC (F.C.), CHRU Pierre-Paul Riquet Hospital, Toulouse; CHU de Strasbourg-Hôpital de Hautepierre (O.L.B., C.T., M.A.); Fédération de Médecine Translationnelle de Strasbourg (FMTS) (O.L.B., C.T., M.A.), Université de Strasbourg; Department of Genetics (A.T., P.C., C.E., M.T., M.-L.M., A.B., F.M., A.D.) and Unit of Biostatistics (S.T.d.M.), APHP Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Charles-Foix University Hospital, Paris; Service de Neurologie (C.M., B.C.), CHRU Gui de Chauliac, Montpellier; Grenoble Alpes (S.H.), Grenoble Institut des Neurosciences; and INSERM (S.H.), U1216, Grenoble, France.

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http://dx.doi.org/10.1212/WNL.0000000000003725DOI Listing
March 2017

Éditorial.

Presse Med 2017 03;46(2 Pt 1):174

Hôpital de Hautepierre, service de neurologie, unité des pathologies du mouvement, 1, avenue Molière, 67000 Strasbourg, France. Electronic address:

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http://dx.doi.org/10.1016/j.lpm.2017.02.001DOI Listing
March 2017

A step toward essential tremor gene discovery: identification of extreme phenotype and screening of HTRA2 and ANO3.

BMC Neurol 2016 Nov 23;16(1):238. Epub 2016 Nov 23.

Service of Neurology, University Hospital of Strasbourg, Hospital of Hautepierre, 1 avenue Molière, 67098, Strasbourg Cedex, France.

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http://dx.doi.org/10.1186/s12883-016-0748-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120508PMC
November 2016

Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia.

J Neurol 2016 Aug 26;263(8):1552-8. Epub 2016 May 26.

Laboratoire de Génétique de Maladies Rares, Institut Universitaire de Recherche Clinique, EA7402, Université de Montpellier, CHU Montpellier, 641 Avenue du Doyen Gaston Giraud, 34093, Montpellier Cedex 5, France.

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http://dx.doi.org/10.1007/s00415-016-8167-3DOI Listing
August 2016

A randomized, controlled, double-blind, crossover trial of zonisamide in myoclonus-dystonia.

Neurology 2016 May 6;86(18):1729-35. Epub 2016 Apr 6.

From Université de la Sorbonne UPMC Paris 06 UMR S 1127 (E.H., M.V., V.B., C.H., D.G., A. Méneret, S. Dupont, E.A., J.-C.C., E.R.), Inserm U 1127, CIC-1422, CNRS UMR 7225, Institut du Cerveau et de la Moëlle, Paris; Département des Maladies du Système Nerveux (E.H., M.V., C.H., B.D., C.B., D.G., J.-C.C., E.R.), Département de Biostatistiques, Unité de Recherche Clinique (N.C., A.B., A. Mallet), Pharmacie (F.C.-B.), Département de Pharmacologie (N.Z.), Département de Génétique, UF de Neurogénétique Moléculaire et Cellulaire (F.C.), and Département d'Epilepsie et de Réhabilitation (S. Dupont), Hôpital Pitié-Salpêtrière, AP-HP; Unité de Neurophysiologie (E.H., E.A.), Département DéPAS, Hôpital Saint-Antoine, AP-HP, Paris; Hospices Civils de Lyon (S.T.), Hôpital Neurologique Pierre Wertheimer; Université Lyon 1 (S.T.); CNRS (S.T.), Centre de Neurosciences Cognitives, UMR 5229, Bron; Département de Neurologie (C.T.), Hôpital de Hautepierre, CHU Strasbourg; Fédération de Médecine translationnelle de Strasbourg (FMTS) (C.T.), Strasbourg, France; Département de Neurologie (G.G.), Hôpital Brugmann, Bruxelles, Belgium; Département de Neurologie (S.Drapier), Hôpital Pontchaillou, CHU Rennes; EA-4712 "Comportement et Noyaux Gris Centraux" (S. Drapier), Université de Rennes 1; Département de Neurologie et Pathologies du Movement (E.M.) and Département de Neurologie (T.L.), CHU de Lille; INSERM UMR-S 1172 (E.M.), Lille; Département de Neurologie (A.D.D.M.), Hôpital Maison Blanche, CHU de Reims; Centre Memoire de Ressources et de Recherche (CMRR) (T.L.), Lille; ESPCI Paris Tech (A.-P.L.), PSL Research University; and Département de Neurologie et Pathologie du Movement (J.-P.A.), Pôle Neurosciences Cliniques, INT-CNRS/AMU Aix-Marseille, France.

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http://dx.doi.org/10.1212/WNL.0000000000002631DOI Listing
May 2016

Homozygosity of the Dominant Myotilin c.179C>T (p.Ser60Phe) Mutation Causes a More Severe and Proximal Muscular Dystrophy.

J Neuromuscul Dis 2016 05;3(2):275-281

Folkhälsan Institute of Genetics and Department of Medical Genetics, Haartman Institute, University of Helsinki, Helsinki, Finland.

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http://dx.doi.org/10.3233/JND-150143DOI Listing
May 2016

Outcome of deep brain stimulation in slowly progressive multiple system atrophy: A clinico-pathological series and review of the literature.

Parkinsonism Relat Disord 2016 Mar 7;24:69-75. Epub 2016 Jan 7.

Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer, Expert Parkinson's Disease Center, 69000 Lyon, France; Université Lyon 1, Faculté de Médecine Lyon Sud Charles Mérieux, 69000 Lyon, France; CNRS, Centre de Neurosciences Cognitives, UMR5229, Bron, France. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2016.01.005DOI Listing
March 2016

Delayed-onset Friedreich's ataxia revisited.

Mov Disord 2016 Jan 21;31(1):62-9. Epub 2015 Sep 21.

Département de Neurologie, Hôpital de Hautepierre, CHU de Strasbourg, France Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM-U964/CNRS-UMR7104/Université de Strasbourg, Illkirch, France; and Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg, France.

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http://dx.doi.org/10.1002/mds.26382DOI Listing
January 2016

ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.

Neurology 2015 Dec 4;85(23):2026-35. Epub 2015 Nov 4.

From the Departments of Neurology (D.-H.C., E.S.B., M.Y.D., P.D.S., M.W., T.D.B.), Psychiatry and Behavioral Sciences (O.K., W.H.R.), Genome Sciences (H.A.S., E.E.E.), Medicine (F.M.H., L.M.A., W.H.R.), and Pathology (M.O.D.), and Howard Hughes Medical Institute (E.E.E.), University of Washington, Seattle; Inserm (A.M., D. Grabli, M.V., O.T., E.R.), U 1127; CNRS (A.M., D. Grabli, M.V., O.T., E.R.), UMR 7225; Sorbonne Université (A.M., D. Grabli, M.V., O.T., E.R.), UPMC Univ Paris 06, UMR S 1127; Institut du Cerveau et de la Moelle Épinière (A.M., D. Grabli, M.V., O.T., E.R.), ICM; Départements de Neurologie (A.M., B.D., D. Grabli, M.V., O.T., E.R.) et de Génétique (C.M.), Hôpital de la Pitié Salpêtrière, AP-HP, Paris, France; the Departments of Neurosciences and Pediatrics (J.R.F.), University of California, San Diego; Rady Childrens Hospital (J.R.F.), San Diego, CA; Tel-Aviv Brill Community Mental Health Center (A.G.), Tel Aviv Medical School, Israel; Service de Neuropédiatrie (D.D.), Hôpital Trousseau, AP-HP; Centre de Référence Mouvements Anormaux de l'Enfant à l'Adulte (D.D.); Centre des Déficiences Intellectuelles de Causes Rares (C.M.), Paris; Département de Neurologie (M.A., C.T.), Hôpital Civil de Strasbourg; Fédération de Médecine Translationnelle de Strasbourg (FMTS) (M.A., C.T.), Université de Strasbourg; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) (M.A., C.T.), INSERM-U964/CNRS-UMR7104/Université de Strasbourg, Illkirch, France; Phoenix Children's Hospital (S.B.), AZ; CHU de Bordeaux (N.D.-P.), Explorations Fonctionnelles du Système Nerveux; Service de Neuropédiatrie (D. Gras), Hôpital Robert Debré, AP-HP, Paris, France; Department of Child Neurology (K.M.M.), Lucile Packard Children's Hospital, Stanford University, Palo Alto, CA; Johns Hopkins All Children's Hospital (S.W.), St. Petersburg, FL; The Scripps Translational Science Institute (A.T.), Scripps Health and The Scripps Research Institute, S

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http://dx.doi.org/10.1212/WNL.0000000000002058DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676753PMC
December 2015

Bedtime-related jerks in the upper limbs associated with restless arms syndrome.

Neurology 2015 Mar;84(9):959

From the Sleep Disorders Center (E.R., U.K.-H., N.C., M.B., P.B.), FMTS, Hôpital Civil, University of Strasbourg; Institute for Cellular and Integrative Neurosciences (E.R., U.K.-H., M.B., P.B.), CNRS-UPR 3212, Strasbourg; and the Center for Movement Disorders (C.T.), Hôpital de Hautepierre, University of Strasbourg, France.

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http://www.neurology.org/content/84/9/959.full.pdf
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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000130
Publisher Site
http://dx.doi.org/10.1212/WNL.0000000000001306DOI Listing
March 2015

Autosomal recessive cerebellar ataxia 3 due to homozygote c.132dupA mutation within the ANO10 gene--reply.

JAMA Neurol 2015 Feb;72(2):239-40

Département de Neurologie, Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, Strasbourg, France.

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http://dx.doi.org/10.1001/jamaneurol.2014.3921DOI Listing
February 2015

Effectiveness of anti-psychotics and related drugs in the Huntington French-speaking group cohort.

PLoS One 2014 15;9(1):e85430. Epub 2014 Jan 15.

Equipe 01, U955, Inserm, Créteil, France ; Faculté de médecine, Université Paris Est, Créteil, France ; Département d'Etudes Cognitives, Ecole Normale Supérieure, Paris, France ; Centre de référence Maladie de Huntington, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0085430PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893200PMC
December 2014

Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study.

JAMA Neurol 2014 Oct;71(10):1305-10

Institut de Génétique et de Biologie Moléculaire et Cellulaire, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Université de Strasbourg, Strasbourg, France9Laboratoire de Génétique des Maladies Rar.

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http://dx.doi.org/10.1001/jamaneurol.2014.193DOI Listing
October 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

The pleiotropic movement disorders phenotype of adult ataxia-telangiectasia.

Neurology 2014 Sep 13;83(12):1087-95. Epub 2014 Aug 13.

From INSERM, UMRS 975, CNRS 7225-CRICM (A.M., E.A., S.R.-P., A.D., M.V., D.G.), AP-HP, Fédération de Neurophysiologie Clinique (B.G., T.M.), AP-HP, Département des Maladies du Système Nerveux (B.D., M.V., D.G.), Département de Génétique et Cytogénétique, Unité Fonctionnelle de Génétique Chromosomique (B.B.), and Département de Génétique et Cytogénétique (A.D., M.A.), Hôpital Pitié-Salpêtrière, Paris; Université Pierre et Marie Curie-Paris-6 (A.M., B.G., E.A., S.R.-P., B.D., A.D., M.V., D.G.); AP-HP, Service de Physiologie (Y.A.-B., E.A.), Hôpital Saint-Antoine; INSERM U830 (G.R., M.-H.S., D.S.-L.), Paris; Unité d'Immuno-Hématologie et Rhumatologie Pédiatriques (N.M., A.F.), CEREDIH (French Reference Center for Primary Immunodeficiencies) (N.M., F.S., A.F.), and Service d'Hématologie Adultes (F.S.), Hôpital Universitaire Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris (APHP); Imagine Institute (N.M., F.S., A.F.), Sorbonne Paris Cité (D.S.-L.), Université Paris Descartes; Département de Neurologie (C.T., M.A.), Hôpital Civil de Strasbourg; Fédération de Médecine Translationnelle de Strasbourg (FMTS) (C.T., M.A.), Université de Strasbourg; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) (C.T., M.K., M.A.), INSERM-U964/CNRS-UMR7104/Université de Strasbourg, Illkirch; Laboratoire de Diagnostic Génétique (M.K.), Nouvel Hôpital Civil, Strasbourg; Laboratoire de Génétique des Maladies Rares (M.K.), INSERM UMR_S 827, Institut Universitaire de Recherche Clinique, Montpellier; and Department of Tumour Biology (M.-H.S., C.D.E., D.S.-L.), Institut Curie, Paris, France.

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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000079
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http://dx.doi.org/10.1212/WNL.0000000000000794DOI Listing
September 2014

The neurophysiological features of myoclonus-dystonia and differentiation from other dystonias.

JAMA Neurol 2014 May;71(5):612-9

Centre de Recherche de l'Institut du Cerveau et de la Moelle Épinière, Institut National de la Santé et de la Recherche Médicale U1127, Centre de Recherche de Neurosciences-Unité Mixte de Recherche 7225, Université Pierre et Marie Curie-Paris 6 UMR_S975.

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http://dx.doi.org/10.1001/jamaneurol.2014.99DOI Listing
May 2014

[Movement disorders].

Rev Prat 2014 Apr;64(4):561-3, 565-7

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April 2014

SPG15: a cause of juvenile atypical levodopa responsive parkinsonism.

J Neurol 2014 Feb 24;261(2):435-7. Epub 2013 Dec 24.

Service de Neurologie, CHU de Strasbourg, Hôpital de Hautepierre, 1, Avenue Molière, 67098, Strasbourg Cedex, France,

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http://link.springer.com/content/pdf/10.1007/s00415-013-7216
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http://link.springer.com/10.1007/s00415-013-7216-4
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http://dx.doi.org/10.1007/s00415-013-7216-4DOI Listing
February 2014

Central nervous system abnormalities in patients with PMP22 gene mutations: a prospective study.

J Neurol Neurosurg Psychiatry 2013 Apr 15;84(4):392-7. Epub 2012 Dec 15.

Department de Neurologie, Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, 1 avenue Molière, Strasbourg 67000, France.

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http://dx.doi.org/10.1136/jnnp-2012-303725DOI Listing
April 2013

[Myasthenia].

Rev Prat 2013 Jan;63(1):109-12

Département de neurologie, pôle tête et cou, CHU Hautepierre, 67098 Strasbourg, France.

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January 2013

Rituximab in refractory and non-refractory myasthenia: a retrospective multicenter study.

Muscle Nerve 2012 Nov 31;46(5):687-91. Epub 2012 Aug 31.

Department of Neurology, University of Strasbourg, University Hospital of Hautepierre, 1 Avenue Molière, 67000 Strasbourg, France.

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http://dx.doi.org/10.1002/mus.23412DOI Listing
November 2012

Exome sequencing reveals SPG11 mutations causing juvenile ALS.

Neurobiol Aging 2012 Apr 10;33(4):839.e5-9. Epub 2011 Dec 10.

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

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http://dx.doi.org/10.1016/j.neurobiolaging.2011.11.012DOI Listing
April 2012

The autosomal recessive cerebellar ataxias.

N Engl J Med 2012 Feb;366(7):636-46

Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Department of Genetics and Cytogenetics, Paris, France.

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http://dx.doi.org/10.1056/NEJMra1006610DOI Listing
February 2012

[Sudden onset sensorimotor deficit: first consider stroke].

Rev Prat 2011 Oct;61(8):1130

Département de neurologie, pôle tête et cou, CHU, Hôpital Civil, 67091 Strasbourg Cedex, France.

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October 2011

POLG1 variations presenting as multiple sclerosis.

Arch Neurol 2010 Sep;67(9):1140-3

Département de Neurologie, Hôpital Civil, 67091 Strasbourg, France.

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http://dx.doi.org/10.1001/archneurol.2010.219DOI Listing
September 2010

Symptomatic paroxysmal dysarthria-ataxia in demyelinating diseases.

J Neurol 2010 Aug 30;257(8):1369-72. Epub 2010 Mar 30.

Département de Neurologie, Hôpital Civil de Strasbourg, 1 Place de l'Hôpital, BP426, 67091 Strasbourg, France.

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http://dx.doi.org/10.1007/s00415-010-5534-3DOI Listing
August 2010

Myopathies in the elderly: a hospital-based study.

Neuromuscul Disord 2010 Jul 1;20(7):443-7. Epub 2010 Jun 1.

Département de Neurologie, Hôpital Civil, BP 426, 67091 Strasbourg, France.

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http://dx.doi.org/10.1016/j.nmd.2010.05.003DOI Listing
July 2010

Follow-up study of the GIGYF2 gene in French families with Parkinson's disease.

Neurobiol Aging 2010 Jun 8;31(6):1069-71; discussion 1072-4. Epub 2009 Dec 8.

INSERM, UMR_S975 (Formerly UMR_S679), Hôpital de la Salpêtrière, Paris, France.

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http://dx.doi.org/10.1016/j.neurobiolaging.2009.06.008DOI Listing
June 2010

Cerebrospinal fluid detection of enterovirus genome in ALS: a study of 242 patients and 354 controls.

Amyotroph Lateral Scler 2010 May;11(3):277-82

Hospices Civils de Lyon, Centre SLA de Lyon (Service d'Electroneuromyographie et Service de Neurologie C), Hôpital Neurologique Pierre Wertheimer, Lyon, France.

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http://dx.doi.org/10.3109/17482960903262083DOI Listing
May 2010

A novel variation in the Twinkle linker region causing late-onset dementia.

Neurogenetics 2010 Feb 10;11(1):21-5. Epub 2009 Jun 10.

Département de Neurologie, Hôpital Civil, BP 426, 67091, Strasbourg, France,

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http://dx.doi.org/10.1007/s10048-009-0202-4DOI Listing
February 2010

Muscle phosphorylase b kinase deficiency revisited.

Neuromuscul Disord 2010 Feb 18;20(2):125-7. Epub 2010 Jan 18.

Département de Neurologie, Hôpital Civil, BP426, 67091 Strasbourg, France.

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http://dx.doi.org/10.1016/j.nmd.2009.11.004DOI Listing
February 2010

[Autosomal recessive cerebellar ataxias].

Presse Med 2009 Dec 12;38(12):1852-9. Epub 2009 May 12.

Clinique neurologique, Hôpitaux universitaires, F-67091 Strasbourg Cedex, France.

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http://dx.doi.org/10.1016/j.lpm.2009.01.025DOI Listing
December 2009

Neuroendocrine disturbances in Huntington's disease.

PLoS One 2009 25;4(3):e4962. Epub 2009 Mar 25.

Centre de référence maladie de Huntington, AP-HP, Groupe Henri-Mondor Albert-Chenevier/Pitié Salpétrière, Créteil, Paris, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0004962PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2655649PMC
July 2009

Association of HLA-A in autoimmune myasthenia gravis with thymoma.

J Neuroimmunol 2009 May 10;210(1-2):120-3. Epub 2009 Mar 10.

Inserm U and Université Paris Descartes, Institut Cochin, Department of Immunology, France.

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https://linkinghub.elsevier.com/retrieve/pii/S01655728090006
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http://dx.doi.org/10.1016/j.jneuroim.2009.02.004DOI Listing
May 2009

Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H.

Neuromuscul Disord 2009 Apr 19;19(4):255-60. Epub 2009 Mar 19.

Laboratoire de diagnostic génétique, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

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http://dx.doi.org/10.1016/j.nmd.2009.02.003DOI Listing
April 2009

SPG11 spastic paraplegia. A new cause of juvenile parkinsonism.

J Neurol 2009 Jan 9;256(1):104-8. Epub 2009 Feb 9.

Dépt. de Neurologie, Hôpital Civil, Centre Hospitalier Universitaire de Strasbourg 1, place de l'Hôpital, 67000 Strasbourg, France.

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http://dx.doi.org/10.1007/s00415-009-0083-3DOI Listing
January 2009

[Myasthenia gravis].

Rev Prat 2008 Dec;58(20):2217-24

Service de neurologie, Hôpitaux universitaires, 67091 Strasbourg Cedex, France.

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December 2008

[Infectious mononeuropathy].

Rev Prat 2008 Nov;58(17):1900-2

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November 2008

Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 families.

Arch Neurol 2008 Jul;65(7):958-62

Département de Neurologie, Hôpital Civil, 1 Place de l'Hôpital, 67091 Strasbourg, France.

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http://dx.doi.org/10.1001/archneur.65.7.958DOI Listing
July 2008

Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutation.

Neuromuscul Disord 2007 Dec 6;17(11-12):955-9. Epub 2007 Sep 6.

Département de Neurologie, Hôpital Civil de Strasbourg, 1 Place de l'Hôpital, BP426, 67091 Strasbourg, France.

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http://dx.doi.org/10.1016/j.nmd.2007.06.467DOI Listing
December 2007

Epidemiologic studies of environmental exposures in Parkinson's disease.

J Neurol Sci 2007 Nov 27;262(1-2):37-44. Epub 2007 Jul 27.

Inserm, U708, Neuroepidemiology, Hôpital de la Salpêtrière, Paris, France.

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http://dx.doi.org/10.1016/j.jns.2007.06.024DOI Listing
November 2007

[Motor and sensory deficit in the limbs].

Rev Prat 2007 Sep;57(13):1481-6; quiz 1486

Département de neurologie, pôle tête et cou, centre hospitalo-universitaire, Hôpital Civil, Strasbourg.

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September 2007

Muscle Nogo-A expression is a prognostic marker in lower motor neuron syndromes.

Ann Neurol 2007 Jul;62(1):15-20

Fédération des Maladies du Système Nerveux, Centre référent maladie rare SLA, Hôpital de la Pitié-Salpêtrière, 47-83 Boulevard de l'Hôpital, 75651 Paris, France.

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http://dx.doi.org/10.1002/ana.21122DOI Listing
July 2007