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Neuromuscular Disorders : NMD|November 5, 2021
Spinal muscular atrophy: from rags to richesEugenio MercuriMuscle & Nerve|March 14, 2024
Survival among patients receiving eteplirsen for up to 8 years for the treatment of Duchenne muscular dystrophy and contextualization with natural history controlsJoel Iff, Nicolae Done, Edward Tuttle, et al.Journal of Neuromuscular Diseases|February 1, 2021
Comparison of Long-term Ambulatory Function in Patients with Duchenne Muscular Dystrophy Treated with Eteplirsen and Matched Natural History ControlsJerry R Mendell, Navid Khan, Nanshi Sha, et al.Current Opinion in Pediatrics|November 19, 2013
Muscular dystrophy: new challenges and review of the current clinical trialsEugenio Mercuri, Francesco MuntoniDevelopmental Medicine and Child Neurology|January 6, 2026
The floppy infant revisited: From bedside to genomeGianpaolo Cicala, Eugenio MercuriAnnals of Neurology|July 26, 2012
The ever-expanding spectrum of congenital muscular dystrophiesEugenio Mercuri, Francesco MuntoniNeurology|July 3, 2020
Suitability of external controls for drug evaluation in Duchenne muscular dystrophyNathalie Goemans, James Signorovitch, Gautam Sajeev, et al.Current Opinion in Pediatrics|November 7, 2024
Treatment of spinal muscular atrophyMaria Carmela Pera, Eugenio MercuriNeural Plasticity|December 3, 2003
Neonatal brain MRI and motor outcome at school age in children with neonatal encephalopathy: a review of personal experienceEugenio Mercuri, Anna L BarnettPageof 62