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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.
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 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.
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.
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.
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.
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 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.
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.
Journal articles
inserm-02426553v1
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Centronuclear Myopathies
Norma B. Romero
,
Marc Bitoun
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 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.
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.
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
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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
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.
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.
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.
Journal articles
inserm-00950634v1
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