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Intramuscular sex steroid hormones are associated with skeletal muscle strength and power in women with different hormonal status

Eija Pöllänen , Reeta Kangas , Mia Horttanainen , Paula Niskala , Jaakko Kaprio , et al.
Aging Cell, 2015, 14 (2), pp.236-248. ⟨10.1111/acel.12309⟩
Journal articles hal-01206197v1
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Multiexon deletions account for 15% of Congenital Myasthenic Syndrome with RAPSN mutations after negative DNA Sequencing

Karen Gaudon , Isabelle Pénisson-Besnier , Brigitte Chabrol , Françoise Bouhour , Laurence Demay , et al.
Journal of Medical Genetics, 2010, 47 (12), pp.795. ⟨10.1136/jmg.2010.081034⟩
Journal articles istex hal-00574007v1
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Identification of an agrin mutation that causes congenital myasthenia and affects synapse function.

Caroline Huzé , Stéphanie Bauché , Pascale Richard , Frédéric Chevessier , Evelyne Goillot , et al.
American Journal of Human Genetics, 2009, 85 (2), pp.155-67. ⟨10.1016/j.ajhg.2009.06.015⟩
Journal articles inserm-00409064v1
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Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization.

J. A. Bevilacqua , Nicole Monnier , Marcus Bitoun , Bruno Eymard , Ana Ferreiro , et al.
Neuropathology and Applied Neurobiology, 2011, 37 (3), pp.271-84. ⟨10.1111/j.1365-2990.2010.01149.x⟩
Journal articles inserm-00639292v1
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In Antisynthetase Syndrome, ACPA Are Associated With Severe and Erosive Arthritis: An Overlapping Rheumatoid Arthritis and Antisynthetase Syndrome

Alain Meyer , Guillaume Lefevre , Guillaume Bierry , Aurélie Duval , Sébastien Ottaviani , et al.
Medicine, 2015, 94 (20), pp.e523. ⟨10.1097/MD.0000000000000523⟩
Journal articles hal-01226438v1
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Online Training on Skin Cancer Diagnosis in Rheumatologists: Results from a Nationwide Randomized Web-Based Survey

Manuelle Viguier , Stéphanie Rist , François Aubin , Marie-Thérèse Leccia , Marie-Aleth Richard , et al.
Journal articles hal-01211398v1
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Quickly progressive amyotrophy of the thigh: An unusual cause of rapid chondrolysis of the knee

Maeva Ferrari , Karine Louati , Anne Miquel , Anthony Behin , Olivier Benveniste , et al.
Joint Bone Spine, 2015, 82 (3), pp.203-205. ⟨10.1016/j.jbspin.2014.12.013⟩
Journal articles hal-01117107v1
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Functional characterization of a Central Core Disease RyR1 mutation (p.Y4864H) associated with quantitative defect in RyR1 protein

Marine Cacheux , Ariane Blum , Muriel Sébastien , Julie Brocard , Kamel Mamchaoui , et al.
Journal of Neuromuscular Diseases, 2015, 202 (4), pp.421-432. ⟨10.3233/JND-150073⟩
Journal articles inserm-01216714v1
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Generation of BAC Transgenic Tadpoles Enabling Live Imaging of Motoneurons by Using the Urotensin II-Related Peptide (ust2b) Gene as a Driver

Marion Bougerol , Frédéric Auradé , François M Lambert , Didier Le Ray , Denis Combes , et al.
PLoS ONE, 2015, 10 (2), pp.e0117370. ⟨10.1371/journal.pone.0117370⟩
Journal articles hal-01230978v1
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Diaphragmatic Function Is Preserved during Severe Hemorrhagic Shock in the Rat

Serge Carreira , Matthieu Le Dinh , Marc Soubeyrand , Marie-Pierre Poloujadoff , Bruno Riou , et al.
Anesthesiology, 2014, 120 (2), pp.425-435. ⟨10.1097/ALN.0000000000000011⟩
Journal articles inserm-02426553v1
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Centronuclear Myopathies

Norma B. Romero , Marc Bitoun
Seminars in Pediatric Neurology, 2011, 18 (4), pp.250-256. ⟨10.1016/j.spen.2011.10.006⟩
Journal articles hal-02451115v1
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Myf5 haploinsufficiency reveals distinct cell fate potentials for adult skeletal muscle stem cells.

Barbara Gayraud-Morel , Fabrice Chrétien , Aurélie Jory , Ramkumar Sambasivan , Elisa Negroni , et al.
Journal of Cell Science, 2012, 125 (Pt 7), pp.1738-49. ⟨10.1242/jcs.097006⟩
Journal articles pasteur-00705770v1
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Automatic solver for non-linear partial differential equations with implicit local laws: Application to unilateral contact

Arnaud Lejeune , Hakim Boudaoud , Michel Potier-Ferry , Isabelle Charpentier , Hamid Zahrouni
International Journal for Numerical Methods in Engineering, 2013, 94, pp.850-867. ⟨10.1002/nme.4483⟩
Journal articles hal-00982813v1
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Phenotypic correction of alpha-sarcoglycan deficiency by intra-arterial injection of a muscle-specific serotype 1 rAAV vector

Françoise Fougerousse , Marc Bartoli , Jérôme Poupiot , Ludovic Arandel , Muriel Durand , et al.
Molecular Therapy, 2007, 15 (1), pp.53-61. ⟨10.1038/⟩
Journal articles hal-01610043v1
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A Centronuclear Myopathy - Dynamin 2 Mutation Impairs Autophagy in Mice

Anne-Cécile Durieux , Stéphane Vassilopoulos , Jeanne Lainé , Bodvael Fraysse , Laura Briñas , et al.
Traffic, 2012, 13 (6), pp.869-879. ⟨10.1111/j.1600-0854.2012.01348.x⟩
Journal articles hal-02453822v1
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Cellular therapies for muscular dystrophies: frustrations and clinical successes

Elisa Negroni , Anne Bigot , Gillian Butler-Browne , Capucine Trollet , Vincent Mouly
Human Gene Therapy, 2015, 27 (2), pp.117-126. ⟨10.1089/hum.2015.139⟩
Journal articles hal-01258690v1
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Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy

Frédérique Rau , Jeanne Lainé , Laetitita Ramanoudjame , Arnaud Ferry , Ludovic Arandel , et al.
Nature Communications, 2015, 6 (1), pp.7205. ⟨10.1038/ncomms8205⟩
Journal articles hal-01162385v1
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Protein kinase D increases maximal Ca 2+ -activated tension of cardiomyocyte contraction by phosphorylation of cMyBP-C-Ser 315

Ellen Dirkx , Olivier Cazorla , Robert Schwenk , Ilka Lorenzen-Schmidt , Sakthivel Sadayappan , et al.
AJP - Heart and Circulatory Physiology, 2012, 303 (3), pp.H323 - H331. ⟨10.1152/ajpheart.00749.2011⟩
Journal articles hal-01824324v1
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An overview of new translational, clinical and therapeutic perspectives in laminopathies and other nuclear envelope-related diseases.

Annachiara de Sandre-Giovannoli , Nicolas Lévy , Rabah Ben Yaou , France Leturcq , Giovanna Lattanzi , et al.
Orphanet Journal of Rare Diseases, 2015, 10 (Suppl 2), ⟨10.1186/1750-1172-10-S2-I1⟩
Journal articles hal-01769449v1
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Inflammation-Induced Acute Phase Response in Skeletal Muscle and Critical Illness Myopathy

Claudia Langhans , Steffen Weber-Carstens , Franziska Schmidt , Jida Hamati , Melanie Kny , et al.
PLoS ONE, 2014, 9 (3), pp.e92048. ⟨10.1371/journal.pone.0092048⟩
Journal articles hal-01365918v1
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Is Adipose Tissue a Place for Mycobacterium tuberculosis Persistence?

Olivier Neyrolles , Rogelio Hernández-Pando , France Pietri-Rouxel , Paul Fornès , Ludovic Tailleux , et al.
PLoS ONE, 2006, 1, pp.e43. ⟨10.1371/journal.pone.0000043⟩
Journal articles pasteur-00130276v1
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DHPR alpha1S subunit controls skeletal muscle mass and morphogenesis.

France Piétri-Rouxel , Christel Gentil , Stéphane Vassilopoulos , Dominique Baas , Etienne Mouisel , et al.
EMBO Journal, 2010, 29 (3), pp.643-54. ⟨10.1038/emboj.2009.366⟩
Journal articles inserm-00515849v1
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Human muscle satellite cells as targets of Chikungunya virus infection.

Simona Ozden , Michel Huerre , Jean-Pierre Riviere , Lark L Coffey , Philippe V Afonso , et al.
PLoS ONE, 2007, 2 (6), pp.e527. ⟨10.1371/journal.pone.0000527⟩
Journal articles pasteur-00292848v1
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A new muscle glycogen storage disease associated with glycogenin-1 deficiency

Edoardo Malfatti , Johanna Nilsson , Carola Hedberg-Oldfors , Aurelio Hernandez-Lain , Fabrice Michel , et al.
Annals of Neurology, 2014, 76 (6), pp.891 - 898. ⟨10.1002/ana.24284⟩
Journal articles hal-01699463v1
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A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia

Asma Ben Ammar , Payam Soltanzadeh , Stéphanie Bauché , Pascale Richard , Evelyne Goillot , et al.
PLoS ONE, 2013, 8 (1), pp.e53826. ⟨10.1371/journal.pone.0053826⟩
Journal articles hal-01537840v1
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Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursors.

Perrine Castets , Svetlana Maugenre , Corine Gartioux , Mathieu Rederstorff , Alain Krol , et al.
BMC Developmental Biology, 2009, 9 (1), pp.46. ⟨10.1186/1471-213X-9-46⟩
Journal articles inserm-00610658v1
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Characterization of thymic hyperplasia associated with autoimmune Myasthenia Gravis : role of the chemokines CXCL12 and CXCL13

Julia Miriam Weiss
Agricultural sciences. Université Paris Sud - Paris XI, 2011. English. ⟨NNT : 2011PA114831⟩
Theses tel-00782854v1
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Muscle histopathology in nebulin-related nemaline myopathy: ultrastrastructural findings correlated to disease severity and genotype.

Edoardo Malfatti , Vilma-Lotta Lehtokari , Johann Böhm , Josine de Winter , Ursula Schäffer , et al.
Acta Neuropathologica Communications, 2014, 2 (1), pp.44. ⟨10.1186/2051-5960-2-44⟩
Journal articles inserm-00987739v1
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An integrated diagnosis strategy for congenital myopathies.

Johann Böhm , Nasim Vasli , Edoardo Malfatti , Stéphanie Le Gras , Claire Feger , et al.
PLoS ONE, 2013, 8 (6), pp.e67527. ⟨10.1371/journal.pone.0067527⟩
Journal articles inserm-00904638v1
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Exploring necrotizing autoimmune myopathies with a novel immunoassay for anti-3-hydroxy-3-methyl-glutaryl-CoA reductase autoantibodies.

Laurent Drouot , Yves Allenbach , Fabienne Jouen , Jean-Luc Charuel , Jérémie Martinet , et al.
Arthritis Research and Therapy, 2014, 16 (1), pp.R39. ⟨10.1186/ar4468⟩
Journal articles inserm-00950634v1