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Giovanni Baranello

Showing results (51-60 of 172) with videos related to

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Developmental Medicine and Child Neurology|February 1, 2022
Evolution of bulbar function in spinal muscular atrophy type 1 treated with nusinersenHarriet Weststrate, Georgia Stimpson, Lily Thomas, et al.
European Journal of Clinical Nutrition|January 17, 2019
Anthropometric measurement standardization for a multicenter nutrition survey in children with spinal muscular atrophySimona Bertoli, Andrea Foppiani, Ramona De Amicis, et al.
Neuromuscular Disorders : NMD|January 23, 2026
285th ENMC international workshop: SMN-associated neurodevelopmental disorder: type 1 spinal muscular atrophy and the brain, 31st January - 2nd February 2025, Hoofddorp, The NetherlandsDavid Gómez-Andrés, Michelle A Farrar, Mireia Alvarez-Molinero, et al.
The Cochrane Database of Systematic Reviews|December 10, 2024
Treatments for RYR1-related disordersSharika Raga, Nicol Voermans, Ivan Perez-Neri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 5, 2024
Understanding North Star Ambulatory Assessment total scores and their implications for standards of care using observational dataGeorgia Stimpson, Meredith K James, Michela Guglieri, et al.
Bone|June 10, 2015
Bone and Spinal Muscular AtrophySilvia Vai, Maria Luisa Bianchi, Isabella Moroni, et al.
Epilepsy Research|November 27, 2010
Early development in Dravet syndrome; visual function impairment precedes cognitive declineDaniela Chieffo, Daniela Ricci, Giovanni Baranello, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 3, 2010
Language abilities and gestural communication in a girl with bilateral perisylvian syndrome: a clinical and rehabilitative follow-upBruna Molteni, Daniela Sarti, Gloria Airaghi, et al.
Clinical Pharmacology and Therapeutics|April 1, 2021
Prognostic Factors and Treatment-Effect Modifiers in Spinal Muscular AtrophyGiovanni Baranello, Ksenija Gorni, Monica Daigl, et al.
Journal of Neuromuscular Diseases|November 19, 2023
Quantifying Variability in Motor Function in Duchenne Muscular Dystrophy: UK Centiles for the NorthStar Ambulatory Assessment, 10 m Walk Run Velocity and Rise from Floor Velocity in GC Treated BoysGeorgia Stimpson, Deborah Ridout, Amy Wolfe, et al.
Pageof 18

Showing results (51-60 of 172) with videos related to

Sort By:
Pageof 18
Developmental Medicine and Child Neurology|February 1, 2022
Evolution of bulbar function in spinal muscular atrophy type 1 treated with nusinersenHarriet Weststrate, Georgia Stimpson, Lily Thomas, et al.
European Journal of Clinical Nutrition|January 17, 2019
Anthropometric measurement standardization for a multicenter nutrition survey in children with spinal muscular atrophySimona Bertoli, Andrea Foppiani, Ramona De Amicis, et al.
Neuromuscular Disorders : NMD|January 23, 2026
285th ENMC international workshop: SMN-associated neurodevelopmental disorder: type 1 spinal muscular atrophy and the brain, 31st January - 2nd February 2025, Hoofddorp, The NetherlandsDavid Gómez-Andrés, Michelle A Farrar, Mireia Alvarez-Molinero, et al.
The Cochrane Database of Systematic Reviews|December 10, 2024
Treatments for RYR1-related disordersSharika Raga, Nicol Voermans, Ivan Perez-Neri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 5, 2024
Understanding North Star Ambulatory Assessment total scores and their implications for standards of care using observational dataGeorgia Stimpson, Meredith K James, Michela Guglieri, et al.
Bone|June 10, 2015
Bone and Spinal Muscular AtrophySilvia Vai, Maria Luisa Bianchi, Isabella Moroni, et al.
Epilepsy Research|November 27, 2010
Early development in Dravet syndrome; visual function impairment precedes cognitive declineDaniela Chieffo, Daniela Ricci, Giovanni Baranello, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 3, 2010
Language abilities and gestural communication in a girl with bilateral perisylvian syndrome: a clinical and rehabilitative follow-upBruna Molteni, Daniela Sarti, Gloria Airaghi, et al.
Clinical Pharmacology and Therapeutics|April 1, 2021
Prognostic Factors and Treatment-Effect Modifiers in Spinal Muscular AtrophyGiovanni Baranello, Ksenija Gorni, Monica Daigl, et al.
Journal of Neuromuscular Diseases|November 19, 2023
Quantifying Variability in Motor Function in Duchenne Muscular Dystrophy: UK Centiles for the NorthStar Ambulatory Assessment, 10 m Walk Run Velocity and Rise from Floor Velocity in GC Treated BoysGeorgia Stimpson, Deborah Ridout, Amy Wolfe, et al.
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