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Nouvelles espérances dans la lutte contre les myopathies (I)NAU, Jean-Yves.Revue médicale suisse. 2005, Vol 1, Num 24, pp 1642-1643, issn 1660-9379, 2 p.Article

Les myopathies = MyopathicsALBANEL, S.Gazette médicale de France (1969). 1986, Vol 93, Num 30, pp 6-13, issn 0016-5557, 4 p.Article

Myopathy as possible side-effect of cyclosporinCHASSAGNE, P; MEJJAD, O; MOORE, N et al.Lancet (British edition). 1989, Vol 2, Num 8671, issn 0140-6736, 1104 [1 p.]Article

La myopathie à bâtonnets: revue générale à propos de 3 observations = Nemaline myopathy: 3 case reports and review of the literaturePAGES, M; RAMOS, J; PAGES, A. M et al.Annales de pathologie (Paris). 1987, Vol 7, Num 3, pp 216-222, issn 0242-6498Article

Myopathies = MyopathiesGAUSSET, P.Revue internationale de pédiatrie. 1988, Num 177, pp 5-48, issn 0048-8135, 40 p.Serial Issue

Principales maladies neuromusculairesREPERE MYOLINE. 2000, 20 p., n° isoléSerial Issue

Atteinte musculaire et glucocorticoïdes : Corticothérapie = Steroid-induced myopathy : CorticosteroidsPERROT, Serge; LE JEUNNE, Claire.La Presse médicale (1983). 2012, Vol 41, Num 4, pp 422-426, issn 0755-4982, 5 p.Article

Collagène VI et maladies musculaires = Collagen type VI-related myopathiesSTOJKOVIC, Tanya.Neurologie.com. 2010, Vol 2, Num 4, issn 2100-9511, p. 105Article

Reversible myopathy and renal impairmentFREESTON, Jane; GOUGH, Andrew.Journal of the Royal Society of Medicine. 2004, Vol 97, Num 3, pp 124-125, issn 0141-0768, 2 p.Article

Epsilon amino caproic acid myopathy: additional featuresVAN RENTERGHEM, D; DE REUCK, J; SCHELSTRAETE, K et al.Clinical neurology and neurosurgery. 1984, Vol 86, Num 3, pp 153-157, issn 0303-8467Article

Myopathie aiguë et hyperthyroïdie = Acute myopathy and hyperthyroidismBOTTACCHI, E; CORNELIO, F; CAMERLINO, M et al.Revue neurologique (Paris). 1986, Vol 142, Num 12, pp 926-927, issn 0035-3787Article

High stature in neonatal myotubular myopathyLEGUENNEC, J.-C; BERNIER, J.-P; LAMARCHE, J et al.Acta paediatrica scandinavica. 1988, Vol 77, Num 4, pp 610-611, issn 0001-656XArticle

Neuropathology of myoclonus epilepsy associated with ragged-red fibers (Fukuhara's disease)TAKEDA, S; KAWABAYASHI, K; OHAMA, E et al.Acta neuropathologica. 1988, Vol 75, Num 5, pp 433-440, issn 0001-6322Article

Myopathies congénitales : NEURO-PÉDIATRIE = Congenital myopathiesQUIJANO-ROY, S; RIVIER, F; ROMERO, N. B et al.La Lettre du neurologue. 2014, Vol 18, Num 7, pp 263-266, issn 1276-9339, 4 p.Article

Les myopathies nécrosantes acquises = Acquired necrotizing myopathiesALLENBACH, Y; BENVENISTE, O.La Revue de médecine interne (Paris). 2013, Vol 34, Num 6, pp 363-368, issn 0248-8663, 6 p.Article

Nutritional consequences of critical illness myopathies : Nutritional consequences of critical illness myopathiesTOBIN, Brian W; UCHAKIN, Peter N.The Journal of nutrition. 2005, Vol 135, Num 7, pp 1803S-1805S, issn 0022-3166Article

Inflammatory myopathies in childrenCOMPEYROT-LACASSAGNE, Sandrine; FELDMAN, Brian M.The Pediatric clinics of North America. 2005, Vol 52, Num 2, pp vi-vii, issn 0031-3955, 30 p.Article

Metabolic myopathiesHIRANO, Michio; DIMAURO, Salvatore.Advances in neurology. 2002, Vol 88, pp 217-234, issn 0091-3952, 18 p.Article

Behandlungskronzepte der physikalischen medizin bei myopathienWEIMANN, G; ARNOLD, C.R; KEMPER, M et al.Kranken Gymnastik. 1991, Vol 43, Num 1, pp 5-7, issn 0023-4494Article

Novel CLN3 mutation causing autophagic vacuolar myopathyCORTESE, Andrea; TUCCI, Arianna; PITTMAN, Alan et al.Neurology. 2014, Vol 82, Num 23, pp 2072-2076, issn 0028-3878, 5 p.Article

Myopathie de Duchenne. Quand une maladie rare aide d'autres pathologiesSCIENCE ET SANTE. 2013, Num 15, issn 2119-9051, 10Article

Statin induced myopathySATHASIVAM, Sivakumar; LECKY, Bryan.BMJ. British medical journal (International ed.). 2008, Vol 337, Num 7679, pp 1159-1162, issn 0959-8146, 4 p.Article

Characterization of recessive RYR1 mutations in core myopathiesHAIYAN ZHOU; YAMAGUCHI, Naohiro; TREVES, Susan et al.Human molecular genetics (Print). 2006, Vol 15, Num 18, pp 2791-2803, issn 0964-6906, 13 p.Article

Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2HSCHOSER, Benedikt G. H; FROSK, Patrick; ENGEL, Andrew G et al.Annals of neurology. 2005, Vol 57, Num 4, pp 591-595, issn 0364-5134, 5 p.Article

Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entityVON DER SLUIJS, B. M; TER LAAK, H. J; SCHEFFER, H et al.Journal of neurology, neurosurgery and psychiatry. 2004, Vol 75, Num 10, pp 1499-1501, issn 0022-3050, 3 p.Article

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