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Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients
Molenaar JP, Verhoeven JI, Rodenburg RJ, et al.
Brain : a journal of neurology, 2020, 143, 2, p 452
New strategy for improving the diagnostic sensitivity of repetitive nerve stimulation in myasthenia gravis
Bou Ali H, Salort-Campana E, Grapperon AM, et al.
Muscle & Nerve, 2017, 55, 4, p 532
Improving molecular diagnosis of distal myopathies by targeted next-generation sequencing
Sevy A, Cerino M, Gorokhova S, et al.
Journal of neurology, neurosurgery, and psychiatry, 2016, 87, 3, p 340
Myofibrillar myopathies: State of the art, present and future challenges
Behin A, Salort-Campana E, Wahbi K, et al.
Revue neurologique, 2015, 171, 10, p 715
Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study
Antoine JC, Robert-Varvat F, Maisonobe T, et al.
Journal of neurology, 2014, 261, 11, p 2093
An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A
Attarian S, Vallat JM, Magy L, et al.
Orphanet journal of rare diseases, 2014, 9
Efficacité du rituximab dans un cas de syndrome de Lambert-Eaton non paranéoplasique séronégatif
Boutin E, Rey C, Romeu M, et al.
Revue de médecine interne (La), 2013, 34, 8, p. 493-496
Correlation of clinicoserologic and pathologic classifications of inflammatory myopathies: study of 178 cases and guidelines for diagnosis
Fernandez C, Bardin N, de Paula AM, et al.
Medicine (Baltimore), 2012, 92, 1, p. 15-24
Myopathies distales : à propos d'une étude rétrospective
Collectif, Franques J, Attarian S, et al.
Revue neurologique (Paris), 2012, 168, Supplt 1, p. S15
Brody syndrome represents a plausible diagnosis for painless exercise-induced stiffness without electrical myotonia : detection of 10 cases related to mutations in ATP2A1 gene
Sternberg D, Chevessier F, Bassez G, et al.
Congrès : 4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France))
2011, p. 145
Evidence for complex repetitive discharges, muscle dystrophy changes and neuromuscular junction remodeling in Schwartz-Jampel syndrome : Communication lors du 4th International Congress of Myology (4ème colloque international de Myologie) 9-13 mai 2011 Lille, France
Nicole S, Franques J, Bauché S, et al.
2011, p 145
A TPM3 mutation causing cap myopathy
de Paula AM, Franques J, Fernandez C, et al.
Neuromuscular disorders : NMD, 2009, 19, 10, p 685
Myasthénie séronégative et myasthénie avec anticorps anti-MuSK : une série rétrospective de 20 cas
Aubert S, Salort-Campana E, Franques J, et al.
Revue neurologique (Paris), 2009, 165, 11, p. 901-910
Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutation
Echaniz-Laguna A, Nicot AS, Carré S, et al.
Neuromuscular disorders : NMD, 2007, 17, 11-12, p. 955-959
