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Natural history of Type 2 and 3 spinal muscular atrophy: 2-year NatHis-SMA study
Annoussamy M, Seferian AM, Daron A, et al.
Annals of clinical and translational neurology, 2020
Re: "Moving Forward After Two Deaths in a Gene Therapy Trial of Myotubular Myopathy" by Wilson and Flotte
Shieh PB, Bonnemann CG, Muller-Felber W, et al.
Human gene therapy, 2020, 31, 15-16, p 787
Nusinersen in patients older than 7 months with spinal muscular atrophy type 1: A cohort study.
Aragon-Gawinska K, Seferian AM, Daron A, et al.
Neurology, 2018, e1312
Prospective and longitudinal natural history study of patients with Type 2 and 3 spinal muscular atrophy: Baseline data NatHis-SMA study.
Chabanon A, Seferian AM, Daron A, et al.
PLoS ONE, 2018, e0201004
EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome
Gargaun E, Seferian AM, Cardas R, et al.
Journal of neurology, 2016, 263, 7, p 1456
Mild clinical presentation in KLHL40-related nemaline myopathy (NEM 8)
Seferian AM, Malfatti E, Bosson C, et al.
Neuromuscular disorders : NMD, 2016, 26, 10, p 712
A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment
Le Moing AG, Seferian AM, Moraux A, et al.
PLoS ONE, 2016, 11, 6
Non-Ambulant Duchenne Patients Theoretically treatable by Exon 53 Skipping have severe Phenotype
Servais L, Montus M, Le Guiner C, et al.
Journal of Neuromuscular Diseases, 2015, 2, 3, p 269
Upper limb strength and function changes during a one-year follow-up in non-ambulant patients with Duchenne Muscular Dystrophy: an observational multicenter trial
Seferian AM, Moraux A, Annoussamy M, et al.
PLoS ONE, 2015, 10, 2
Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial
Seferian AM, Moraux A, Canal A, et al.
PLoS ONE, 2015, 10, 4
Congenital muscular dystrophy phenotype with neuromuscular spindles excess in a 5-year-old girl caused by HRAS mutation.
Bolocan A, Quijano-Roy S, Seferian AM, et al.
Neuromuscular disorders : NMD, 2014, 24, 11, p 993
