Publications by authors named "Francois Rivier"

77Publications

Menkes disease, a diagnosis to consider in case of severe epilepsy with hyperlactacidemia: a case report.

Ann Biol Clin (Paris) 2020 Aug;78(4):441-445

Département de biochimie et hormonologie, CHU Montpellier, France, PhyMedExp, Université de Montpellier (UM), Inserm, CNRS, Montpellier, France.

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http://dx.doi.org/10.1684/abc.2020.1566DOI Listing
August 2020

The 2020 version of the gene table of neuromuscular disorders (nuclear genome).

Neuromuscul Disord 2019 12 6;29(12):980-1018. Epub 2019 Nov 6.

CHRU de Montpellier, Direction de la Recherche et de l'Innovation, Hôpital La Colombière, Montpellier, France.

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http://dx.doi.org/10.1016/j.nmd.2019.10.010DOI Listing
December 2019

Impaired glycinergic transmission in hyperekplexia: a model of parasomnia overlap disorder.

Ann Clin Transl Neurol 2019 09 7;6(9):1900-1904. Epub 2019 Aug 7.

Département de Neurologie, Unité des Troubles du Sommeil, CHU Montpellier, Montpellier, France.

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http://dx.doi.org/10.1002/acn3.50866DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764621PMC
September 2019

Neurodevelopmental problems of unaccompanied refugee and migrant children: a new challenge for pediatric neurologists.

Dev Med Child Neurol 2019 11 10;61(11):1348. Epub 2019 Jun 10.

Department of Clinical and Biomedical Sciences L. Sacco, University of Milan, Milan, Italy.

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http://dx.doi.org/10.1111/dmcn.14275DOI Listing
November 2019

Phase Contrast MRI Suggests an Internal Carotid Vascular Tone Alteration in Migraines.

Neuropediatrics 2019 08 6;50(4):244-247. Epub 2019 Jun 6.

I2FH, Institut d'Imagerie Fonctionnelle Humaine, Gui de Chauliac Hospital, Montpellier, France.

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http://dx.doi.org/10.1055/s-0039-1692215DOI Listing
August 2019

A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management.

Neurology 2019 02 18;92(8):e852-e865. Epub 2019 Jan 18.

From CHRU de Tours (E.L.), Université François Rabelais de Tours, INSERM U1253, Tours; Neuromuscular Reference Center (C.D., M.D.A., R.G.), AP-HP, Hôpital Pitié-Salpêtrière, Paris; Inserm UMRS872 (M.D.A.), team22, Centre de recherche des Cordeliers, Paris; Service de neurologie pédiatrique (F.A.), pneumologie pédiatrique et médecine infantile, Hôpital de La Timone, Marseille; Service de pédiatrie médicale (N.B.), pôle Femme Enfant, CHU, Caen; Consultation myologie (C.B., I.D.), Cliniques des maladies du développement, Hôpital Necker-Enfants Malades, Paris; Centre hospitalier universitaire de Fort de France (R.B.), unité de neuromyologie, Fort de France; Service de pédiatrie-Neurologie Pôle enfants (C.C.), Hôpital des enfants, CHU Purpan, Toulouse; Service de neurologie pédiatrique (B.C.), pneumologie pédiatrique et médecine infantile, Hôpital de La Timone, Marseille; Service de Neuropédiatrie et Centre de Référence Maladies Neuromusculaires (J.-M.C.), Hôpital Roger-Salengro, Lille; Pôle mère-enfant (J.D.), neuropédiatrie et neurochirgurgie de l'enfant, CHU d'Angers; Service de pédiatrie médicale (C.E.), Hôpital Pellegrin, Bordeaux; Pôle de pédiatrie médico-chirurgicale et génétique Clinique (M.F.), CHU de Rennes-Hôpital Sud, Rennes; Centre de Référence Déficiences Intellectuelles (D. Héron), Département de Génétique et INSERM U975, Groupe hospitalier Pitié-Salpétrière, Paris; Service de neuropédiatrie et pathologie du développement (A.I., M.M.), Hôpital Trousseau, Paris; Service de neurophysiologie enfants et adultes (A.J.-P.), Hôpital F. Mitterrand, Dijon; Centre hospitalier Bretagne Atlantique (H.J.), Vannes; Hôpital de la mère et de l'enfant (C.L.-R.), Dominique Larrey, Limoges; Service de pédiatrie 1 (V.L.), Centre de référence pour les maladies neuromusculaires CENRNEST, Hôpital de Hautepierre-Hôpitaux Universitaires de Strasbourg; CHU Nantes (A.M., Y.P., J.P.-B.), Centre de Référence Maladies Neuromusculaires Nantes-Angers, Hôtel-Dieu, Nantes; Service d'Epileptologie Clinique (V.M.), des Troubles du Sommeil et de Neurologie Fonctionnelle de l'Enfant, Hôpital Femme Mère Enfant, Lyon; Département de pédiatrie et département de génétique médicale (S.P.), Hôpital Morvan, Brest; Département de pédiatrie (S.Q.-R.), Hôpital Raymond Poincaré, Garches; Service d'explorations fonctionnelles pédiatriques (S.R.-M.), Hôpital de Brabois, Vandœuvre-Lès-Nancy; Service de de pédiatrie et de neuropédiatrie (C.R.), Hôpital l'Archet 2, Pôle Femme Mère Enfant, Nice; Département de neuropédiatrie (F.R., U.W.-L.), Hôpital Gui de Chauliac, Montpellier; Service de pédiatrie A-Unité de neurologie pédiatrique (P.S.), American Memorial Hospital, Reims; Centre de référence des neuropathies rares et pathologies neuromusculaires (C.S.), Centre hospitalo-universitaire de Clermont-Ferrand, Clermont-Ferrand; Pôle de Psychiatrie (H.T.), Neurologie et Rééducation Neurologique, CHU Grenoble Alpes, Grenoble; Service de neurologie pédiatrique (C.V.), Pavillon Femme, mère et enfant, Hôpital Charles Nicolle, Rouen; Inserm UMR U955 E10 et Université Paris-Est Créteil (R.G.); Direction de la Recherche et de l'Innovation (D. Hamroun), CHRU de Montpellier; Sorbonne Université (G.B.), INSERM, UMRS974, Neuromuscular Reference Center, AP-HP, Hôpital Pitié-Salpêtrière, Paris; and FILNEMUS (E.L., C.D., M.D.A., F.A., N.B., C.B., R.B., C.C., B.C., J.-M.C., I.D., J.D., C.E., M.F., D. Héron, A.I., A.J.-P., H.J., C.L.-R., V.L., A.M., V.M., M.M., Y.P., J.P.-B., S.P., S.Q.-R., S.R.-M., C.R., F.R., P.S., C.S., H.T., C.V., U.W.-L., R.G., D. Hamroun, G.B.), French Neuromuscular Reference Centers, France.

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http://dx.doi.org/10.1212/WNL.0000000000006948DOI Listing
February 2019

The 2019 version of the gene table of neuromuscular disorders (nuclear genome).

Neuromuscul Disord 2018 12 27;28(12):1031-1063. Epub 2018 Sep 27.

CHRU de Montpellier, Direction de la Recherche et de l'Innovation, Hôpital La Colombière, Montpellier, France.

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http://dx.doi.org/10.1016/j.nmd.2018.09.006DOI Listing
December 2018

The 2018 version of the gene table of monogenic neuromuscular disorders (nuclear genome).

Neuromuscul Disord 2017 12 23;27(12):1152-1183. Epub 2017 Nov 23.

CHRU de Montpellier, Direction de la Recherche et de l'Innovation, Hôpital La Colombière, 39 Avenue Charles Flahault, Montpellier 34295, France.

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http://dx.doi.org/10.1016/j.nmd.2017.10.005DOI Listing
December 2017

A Reliable Targeted Next-Generation Sequencing Strategy for Diagnosis of Myopathies and Muscular Dystrophies, Especially for the Giant Titin and Nebulin Genes.

J Mol Diagn 2018 07 21;20(4):533-549. Epub 2018 May 21.

Molecular Diagnostic Laboratory, Centre Hospitalier Universitaire Montpellier, Montpellier, France; AOC (Atlantique-Occitanie-Caraïbe) Reference Center for Neuromuscular Disorders, Aquitaine, France; Rare Diseases Genetics Laboratory, Equipe Accueil EA7402, Université de Montpellier, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.jmoldx.2018.04.001DOI Listing
July 2018

Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.

Am J Hum Genet 2018 05 12;102(5):744-759. Epub 2018 Apr 12.

Service de Génétique Médicale, CHU Nantes, 9 quai Moncousu, 44093 Nantes Cedex 1, France; l'institut du thorax, INSERM, CNRS, UNIV Nantes, 44007 Nantes, France. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2018.02.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5986661PMC
May 2018

AP4 deficiency: A novel form of neurodegeneration with brain iron accumulation?

Neurol Genet 2018 Feb 24;4(1):e217. Epub 2018 Jan 24.

Département de Neuropédiatrie (A.R., B.E., P.M., F.R.), CHU Gui de Chauliac, Montpellier; Institut des Neurosciences de Montpellier (A.R., N.H., G.M., C.P.H.), INSERM U1051, Université de Montpellier; Service de Neuroradiologie (C.-J.R., N.L.), CHU Gui de Chauliac, Montpellier; Equipe MitoLab (M.C., G.L.), UMR CNRS 6015-INSERM 1083, Institut MitoVasc, University of Angers, France; Department of Medical Genetics (C. Goizet), Hopital Pellegrin, Bordeaux University Hospital; MRGM Laboratory (C. Goizet), INSERM U1211, University of Bordeaux; Laboratoire de Génétique Moléculaire (C. Guissart), CHU de Montpellier; U1046 INSERM (P.M., F.R.), UMR9214 CNRS, Université de Montpellier; Department of Neurology (C.M.), University Hospital Gui de Chauliac, Montpellier; Centre de Référence des Malformations et Maladies Congénitales du Cervelet (L.B.), Service de Génétique, Hôpital Armand Trousseau, AP-HP, Paris, France; Wellcome Trust Centre for Mitochondrial Research (R.H.), Institute of Genetic Medicine, Newcastle University, United Kingdom; and Centre of Reference for Genetic Sensory Diseases (C.P.H.), Montpellier, France.

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http://dx.doi.org/10.1212/NXG.0000000000000217DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820597PMC
February 2018

Outcome of isolated agenesis of the corpus callosum: A population-based prospective study.

Eur J Paediatr Neurol 2018 Jan 5;22(1):82-92. Epub 2017 Sep 5.

Université de Lyon, F-69008 Lyon, France; Radiologie pédiatrique et médecine fœtale, Hôpital Femme Mère Enfant, F-69677 Bron, France.

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http://dx.doi.org/10.1016/j.ejpn.2017.08.003DOI Listing
January 2018

Interhypothalamic adhesion and multiple cerebral abnormalities in a 2-year-old boy.

J Neuroradiol 2017 Feb 24;44(1):63-64. Epub 2016 Nov 24.

Département de Neuroradiologie, Hôpital Gui-de-Chauliac, CHRU de Montpellier, 34000 Montpellier, France; Département d'Imagerie Pédiatrique, Hôpital Arnaud-de-Villeneuve, CHU de Montpellier, 34000 Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.neurad.2016.09.001DOI Listing
February 2017

Role of neuroimaging in the diagnosis of hereditary cerebellar ataxias in childhood.

J Neuroradiol 2016 Jun 25;43(3):176-85. Epub 2016 Apr 25.

University Hospital of Montpellier, Department of Neuroradiology, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.neurad.2016.03.006DOI Listing
June 2016

Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmia.

Am J Med Genet A 2016 07 22;170(7):1895-8. Epub 2016 Apr 22.

CHU Toulouse, Service de Génétique Médicale, Hôpital Purpan, Toulouse, France.

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http://dx.doi.org/10.1002/ajmg.a.37667DOI Listing
July 2016

Systematic MRI in NF1 children under six years of age for the diagnosis of optic pathway gliomas. Study and outcome of a French cohort.

Eur J Paediatr Neurol 2016 Mar 17;20(2):275-281. Epub 2015 Dec 17.

Hôpital des Enfants, CHU Purpan, Toulouse, France; Inserm, Imagerie Cérébrale et Handicaps Neurologiques UMR 825, CHU Purpan, Toulouse, France; Université de Toulouse III - Paul Sabatier, Toulouse, France. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2015.12.002DOI Listing
March 2016

A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis.

Neurology 2016 Jan 11;86(2):161-9. Epub 2015 Dec 11.

From UMR7370 CNRS (K.H., S.G., S.B.), LP2M, Labex ICST, University Nice Sophia-Antipolis, Faculté de Médecine, Nice, France; Centre de Recherche (H.P., M.C.), Institut Universitaire en Santé Mentale de Québec; Department of Medicine (H.P., M.C.), Université Laval, Québec City, Canada; CHRU Montpellier (F.R., R.J.M., B.E.), Neuropédiatrie & Centre de Référence Maladies Neuromusculaires, Montpellier; Université de Montpellier (F.R., B.E.); INSERM (F.R.), U1046, CNRS, UMR9214, Montpellier; INSERM (D.S., B.F., B.E., S.N.), U1127, Paris; Sorbonne Universités (D.S., B.F., B.E., S.N.), UPMC University Paris 6, UMR S1127; CNRS (D.S., B.F., B.E., S.N.), UMR 7225, Paris; Institut du Cerveau et de la Moelle Épinière (D.S., B.F., B.E., S.N.), ICM, Paris; AP-HP (D.S., B.F., B.E.), Centres de Référence des Canalopathies Musculaires et des Maladies Neuro-musculaires Paris-Est, Service de Biochimie Métabolique, Hôpital de la Pitié Salpêtrière, France; and MRC Centre for Neuromuscular Diseases (L.K., M.G.H., R.M.), UCL Institute of Neurology, London, UK.

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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.0000000000002264DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731685PMC
January 2016

Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability.

Hum Mol Genet 2015 Jul 21;24(14):3948-55. Epub 2015 Apr 21.

Institut des Neurosciences de Montpellier, Université de Montpellier I et II, BP 74103, 34 091 Montpellier Cedex 5, France, Service de Neuropédiatrie, CHU Gui de Chauliac, 34 295 Montpellier, France,

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http://dx.doi.org/10.1093/hmg/ddv133DOI Listing
July 2015

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.

PLoS Genet 2014 Sep 4;10(9):e1004580. Epub 2014 Sep 4.

Institut Pasteur, Human Genetics and Cognitive Functions Unit, Paris, France; CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France; University Paris Diderot, Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Paris, France; FondaMental Foundation, Créteil, France.

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http://dx.doi.org/10.1371/journal.pgen.1004580DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154644PMC
September 2014

Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability.

Eur J Hum Genet 2014 Feb 15;22(2):289-92. Epub 2013 May 15.

Departement de Genetique Medicale, Centre de Reference Maladies Rares Anomalies du Developpement et Syndromes Malformatifs Sud-Languedoc Roussillon, Hopital Arnaud de Villeneuve CHRU Montpellier, Faculte de Medecine Universite Montpellier 1, Montpellier, France.

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http://dx.doi.org/10.1038/ejhg.2013.113DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895633PMC
February 2014

Natural history of Barth syndrome: a national cohort study of 22 patients.

Orphanet J Rare Dis 2013 May 8;8:70. Epub 2013 May 8.

AP-HP, Registre français des neutropénies chroniques sévères, Centre de référence des déficits Immunitaires Héréditaires, Service d'Hémato-oncologie Pédiatrique Hôpital Trousseau, Paris, France.

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http://dx.doi.org/10.1186/1750-1172-8-70DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656783PMC
May 2013

Prevalence and timing of pregnancy termination for brain malformations.

Arch Dis Child Fetal Neonatal Ed 2011 Sep 19;96(5):F360-4. Epub 2011 Jan 19.

Department of Pathology, Lapeyronie Hospital, Montpellier, France.

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http://dx.doi.org/10.1136/adc.2010.201483DOI Listing
September 2011

Benign paroxysmal vertigo of childhood: long-term outcome.

Cephalalgia 2011 Mar 17;31(4):439-43. Epub 2010 Sep 17.

Department of Neurology, Gui de Chauliac University Hospital, France.

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https://www.mm3admin.co.za/documents/docmanager/6e64f7e1-715
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http://cep.sagepub.com/cgi/doi/10.1177/0333102410382797
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http://dx.doi.org/10.1177/0333102410382797DOI Listing
March 2011

POLG exon 22 skipping induced by different mechanisms in two unrelated cases of Alpers syndrome.

Mitochondrion 2011 Jan 4;11(1):223-7. Epub 2010 Aug 4.

Centre de Biologie et de Pathologie Est - CHU Lyon, Service des Maladies Héréditaires du Métabolisme, 69677 Bron, France.

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http://dx.doi.org/10.1016/j.mito.2010.07.011DOI Listing
January 2011

[Convulsions of infants and children].

Rev Prat 2010 Apr;60(4):543-50

Université Montpellier-1, UFR de medecine, 34295 Montpellier Service de neuropédiatrie, CHU Montpellier, hôpital Gui-de-Chauliac, 34295 Montpellier, France.

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April 2010

Biochemical properties of gastrokine-1 purified from chicken gizzard smooth muscle.

PLoS One 2008 5;3(12):e3854. Epub 2008 Dec 5.

INSERM ERI 25 Muscle et Pathologies, Université Montpellier 1, EA 4202, CHU Arnaud de Villeneuve, Montpellier, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0003854PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2588339PMC
January 2009

Monoamine metabolism study in severe, early-onset epilepsy in childhood.

Epileptic Disord 2008 Jun;10(2):130-5

Child Neurology Department, Université de Montpellier, France.

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http://dx.doi.org/10.1684/epd.2008.0181DOI Listing
June 2008

Myotonic dystrophy type I in childhood Long-term evolution in patients surviving the neonatal period.

Eur J Paediatr Neurol 2008 May 24;12(3):210-23. Epub 2007 Sep 24.

Service de Neuropédiatrie, Centre hospitalier universitaire de Montpellier, France.

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http://dx.doi.org/10.1016/j.ejpn.2007.07.014DOI Listing
May 2008

Modulation of p38 mitogen-activated protein kinase cascade and metalloproteinase activity in diaphragm muscle in response to free radical scavenger administration in dystrophin-deficient Mdx mice.

Am J Pathol 2007 Feb;170(2):633-43

Institut National de la Santé, et de la Recherche Médicale, Equipe ERI 25, Muscle et Pathologies, Université de Montpellier1, Unité de Formation et de Recherche de Médecine, EA701, 4 Boulevard Henri IV, 34060 Montpellier, France.

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http://dx.doi.org/10.2353/ajpath.2007.060344DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1851881PMC
February 2007

Deleterious mutations in exon 1 of MECP2 in Rett syndrome.

Eur J Med Genet 2006 Jul-Aug;49(4):313-22. Epub 2005 Dec 20.

Laboratoire de Génétique, EA 3441, CHU Brabois, avenue du Morvan, 54511 Vandoeuvre-les-Nancy cedex, France.

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http://dx.doi.org/10.1016/j.ejmg.2005.11.002DOI Listing
September 2006

Pathological pattern of Mdx mice diaphragm correlates with gradual expression of the short utrophin isoform Up71.

Biochim Biophys Acta 2006 Mar;1762(3):362-72

Université Montpellier 1, UFR de Médecine, Laboratoire de Physiologie des Interactions, EA 701, Institut de Biologie, Boulevard Henri IV, 34062, Montpellier France

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http://dx.doi.org/10.1016/j.bbadis.2005.11.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1974843PMC
March 2006

Mutation spectrum leading to an attenuated phenotype in dystrophinopathies.

Eur J Hum Genet 2005 Dec;13(12):1254-60

Laboratoire de Génétique Moleculaire et Chromosomique, CHU de Montpellier, Montpellier, France.

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http://dx.doi.org/10.1038/sj.ejhg.5201478DOI Listing
December 2005

The effect of respiratory muscle training with CO2 breathing on cellular adaptation of mdx mouse diaphragm.

Neuromuscul Disord 2005 Jun 18;15(6):427-36. Epub 2005 Apr 18.

Laboratoire de Physiologie des Interactions, EA 701, Service Central de Physiologie Clinique, Hôpital Arnaud de Villeneuve, 34295 Montpellier Cedex 5, France.

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http://dx.doi.org/10.1016/j.nmd.2005.01.014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1978214PMC
June 2005

A comparison of gait in spinal muscular atrophy, type II and Duchenne muscular dystrophy.

Gait Posture 2005 Jun;21(4):369-78

Laboratoire d'Automatique, de Mécanique et d'Informatique industrielles et Humaines, Université de Valenciennes et du Hainaut-Cambrésis, Le Mont Houy, 59313 Valenciennes Cedex 9, France.

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http://dx.doi.org/10.1016/j.gaitpost.2004.04.006DOI Listing
June 2005

alpha7B integrin changes in mdx mouse muscles after L-arginine administration.

FEBS Lett 2005 Feb;579(5):1079-84

EA 701, Muscles et Pathologies Chroniques, Institut de Biologie, Boulevard Henri IV, 34060 Montpellier, France.

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http://dx.doi.org/10.1016/j.febslet.2004.12.081DOI Listing
February 2005

Successful management of cataplexy with intravenous immunoglobulins at narcolepsy onset.

Ann Neurol 2004 Dec;56(6):905-8

Service de Neurologie B, Hôpital Gui-de-Chauliac, Montpellier, France.

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http://dx.doi.org/10.1002/ana.20339DOI Listing
December 2004

The role of muscle biopsy in analysis of the dystrophin gene in Duchenne muscular dystrophy: experience of a national referral centre.

Neuromuscul Disord 2004 Oct;14(10):650-8

Laboratoire de Génétique Moleculaire et Chromosomique, Institut Universitaire de Recherche Clinique (IURC), CHU de Montpellier, 641 avenue du Doyen G. Giraud, 34093 Montpellier Cedex 5, France.

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http://dx.doi.org/10.1016/j.nmd.2004.05.002DOI Listing
October 2004

Congenital club foot with survival of motor neuron 1, telomeric (SMN1) gene deletion.

J Child Neurol 2004 Mar;19(3):212-3

Service de Neuropédiatrie, Hôpital Saint-Eloi, Montpellier, France.

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March 2004

Role of bone marrow cell trafficking in replenishing skeletal muscle SP and MP cell populations.

J Cell Sci 2004 Apr 30;117(Pt 10):1979-88. Epub 2004 Mar 30.

Division of Genetics, Children's Hospital Boston, MA 02115, USA.

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http://dx.doi.org/10.1242/jcs.01051DOI Listing
April 2004

Ataxia with vitamin E deficiency and severe dystonia: report of a case.

Brain Dev 2003 Sep;25(6):442-5

Service de Neuropédiatrie, Hôpital Saint Eloi, 80 Avenue Augustin Fliche, 34295 Montpellier Cedex 5, France.

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http://dx.doi.org/10.1016/s0387-7604(03)00054-8DOI Listing
September 2003

Dose-dependent effect of individualized respiratory muscle training in children with Duchenne muscular dystrophy.

Neuromuscul Disord 2002 Aug;12(6):576-83

Laboratoire de Physiologie des Interactions, Service Central de Physiologie Clinique, Hôpital Arnaud de Villeneuve, 34295 Cedex 5, Montpellier, France.

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http://dx.doi.org/10.1016/s0960-8966(02)00005-6DOI Listing
August 2002