La science face au handicap : un champ de recherche à construire. : Recherche, éthiqueRAVAUD, Jean-François; FARDEAU, Michel.Quelles trajectoires d'insertion pour les personnes handicapées ?. 2007, pp 125-131, 7 p.Book Chapter

Histopathologie et mitochondriopathies. Apport de i'analyse histopathologique musculaire à l'étude des maladies mitochondrialesROMERO, Norma Beatriz; FARDEAU, Michel.Annales de l'Institut Pasteur. Actualités. 2001, Num 9-10, pp 7-23, issn 0924-4204Article

Déficience du Management face au handicap. Du jeu d'acteur aux réponses managériales = MANAGEMENT ORGANISATION AND DISABLED PEOPLEKerroumi, Bachir; Fardeau, Michel.2001, 201 p.Thesis

RECONSTITUTION MUSCULAIRE ET COMPLEMENTATION GENIQUE DANS UN MODELE EXPERIMENTAL ET DES MODELES ANIMAUX DYSTROPHIQUES = MUSCLE RECONSTRUCTION AND GENETIC COMPLEMENTATION IN AN EXPERIMENTAL MODEL AND IN DYSTROPHIC ANIMAL MODELSAlameddine, Hala; Fardeau, Michel.1998, 283 p.Thesis

Aspects scientifiques = Scientific evaluation of AFMCADORET, René; FARDEAU, Michel; MANARANCHE, Robert et al.Réadaptation (Paris). 1992, Num 394, pp 5-20, issn 0484-0305Serial Issue

Social identity and the International Classification of Handicaps : an evaluation of the consequences of facioscapulohumeral muscular dystrophy = L'identité sociale et la Classification internationale des Handicaps : évaluation des conséquences de la dystrophie musculaire facioscapulohumeralVILLE, I; RAVAUD, J.F; MARCHAL, F et al.Disability and rehabilitation. 1992, Num 4, pp 168-175Article

Etude des métalloprotéases MMP-2 et MMP-9 au cours de la régénération, de la réinnervation et du développement du muscle squelettique de souris = Matrix metalloproteinases, MMP-2 and MMP-9 expression during regeneration, reinnervation and development of mouse skeletal muscleAit Amer Belkacem Kherif, Sonia; Fardeau, Michel.1999, 165 p.Thesis

Local Dystrophin Restoration with Antisense Oligonucleotide PR0051PLAISIER, Emmanuelle; GRIBOUVAL, Olivier; DRACON, Michel et al.The New England journal of medicine. 2007, Vol 357, Num 26, pp 2687-2695, issn 0028-4793, 9 p.Article

A propos d'un essai de Phase I de thérapie génique effectué avec un plasmide contenant l'intégralité du gène dystrophine dans la Myopathie de Duchenne/Becker = About a Phase I gene therapy clinical trial with a full-length dystrophin gene-plasmid in Duchenne/Becker Muscular DystrophyFARDEAU, Michel; BRAUN, Serge; ROMERO, Norma B et al.Journal de la Société de biologie. 2005, Vol 199, Num 1, pp 29-32, issn 1295-0661, 4 p.Conference Paper

Age-related morphological changes of the deltoid muscle from 50 to 79 years of ageFAYET, Guillemette; ROUCHE, Andrée; HOGREL, Jean-Yves et al.Acta neuropathologica. 2001, Vol 101, Num 4, pp 358-366, issn 0001-6322Article

Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disordersSTERNBERG, Damien; CHATZOGLOU, Evi; LAFORET, Pascal et al.Brain. 2001, Vol 124, pp 984-994, issn 0006-8950, 5Article

Désingulariser le handicap ? Quelles ruptures pour quelles mutations culturelles ?GARDOU, Charles; POIZAT, Denis; PUIG, José et al.2007, 360 p.Book

Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N geneFERREIRO, Ana; GROOTE, Chantal Ceuterick-De; GUICHENEY, Pascale et al.Annals of neurology. 2004, Vol 55, Num 5, pp 676-686, issn 0364-5134, 11 p.Article

Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesiaROMERO, Norma Beatriz; MONNIER, Nicole; VIOLLET, Louis et al.Brain. 2003, Vol 126, pp 2341-2349, issn 0006-8950, 9 p., 11Article

Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: Reassessing the nosology of early-onset myopathiesFERREIRO, Ana; QUIJANO-ROY, Susana; ROMERO, Norma B et al.American journal of human genetics. 2002, Vol 71, Num 4, pp 739-749, issn 0002-9297, 11 p.Article

An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptorMONNIER, Nicole; ROMERO, Norma Beatriz; LERALE, Joëlle et al.Human molecular genetics (Print). 2000, Vol 9, Num 18, pp 2599-2608, issn 0964-6906Article

Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse FunctionHUZE, Caroline; BAUCHE, Stéphanie; BERNARD, Véronique et al.American journal of human genetics. 2009, Vol 85, Num 2, pp 155-167, issn 0002-9297, 13 p.Article

Caractérisation physiopathologique des syndromes myasthéniques congénitaux : l'exemple de mutations dans le gène MUSK = Pathophysiological characterization of congenital myasthenic syndromes : the example of mutations in the MUSK geneCHEVESSIER, Frédéric; FARAUT, Brice; AZULAY, Jean-Philippe et al.Journal de la Société de biologie. 2005, Vol 199, Num 1, pp 61-77, issn 1295-0661, 17 p.Conference Paper

Late-onset mitochondrial DNA depletion : DNA copy number, multiple deletions, and compensationBARTHELEMY, Cyrille; OGIER DE BAULNY, Hélène; DIAZ, Jorge et al.Annals of neurology. 2001, Vol 49, Num 5, pp 607-617, issn 0364-5134Article

X-linked vacuolated myopathy: TNF-α and IFN-γ expression in muscle fibers with mhc class I on sarcolemmaROUGER, Karl; LOUBOUTIN, Jean-Pierre; VILLANOVA, Marcello et al.The American journal of pathology. 2001, Vol 158, Num 2, pp 355-359, issn 0002-9440Article

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2i as a milder allelic variant of congenital muscular dystrophy MDC1CBROCKINGTON, Martin; YUVA, Yeliz; FALLET, Shari et al.Human molecular genetics (Print). 2001, Vol 10, Num 25, pp 2851-2859, issn 0964-6906Article

Multi-minicore disease-searching for boundaries: Phenotype analysis of 38 casesFERREIRO, Ana; ESTOURNET, Brigitte; HAENGGELI, Charles-Antoine et al.Annals of neurology. 2000, Vol 48, Num 5, pp 745-757, issn 0364-5134Article

Handicap : une ère nouvelle. Compensation et libre choixGILLOT, Dominique; LYAZID, Maryvonne; SANCHEZ, Jésus et al.Réadaptation (Paris). 2000, Num 471, pp 3-58, issn 0484-0305Article

Characterization of the muscle involvement in dynamin 2-related centronuclear myopathyFISCHER, Dirk; HERASSE, Muriel; BITOUN, Marc et al.Brain. 2006, Vol 129, pp 1463-1469, issn 0006-8950, 7 p., 6Article

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