Mariacristina Scoto

Revised upper limb module for spinal muscular atrophy: Development of a new module

Elena Mazzone, Anna Mayhew, Jacqueline Montes et al. · Muscle & Nerve · 2016 · 362 citations

Medicine, Neurology, Rehabilitation Medicine +14

Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations

Valeria Ricotti, William Mandy, Mariacristina Scoto et al. · Developmental Medicine & Child Neurology · 2015 · 322 citations

Medicine, Genetics, Pediatrics +17

Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre, phase 3 trial

Eugenio Mercuri, Francesco Muntoni, Giovanni Baranello et al. · The Lancet Neurology · 2021 · 256 citations

Medicine, Neurology, Neuroscience +12

Mutations in the tail domain of <i>DYNC1H1</i> cause dominant spinal muscular atrophy

Matthew B. Harms, Kassandra M Ori-McKenney, Mariacristina Scoto et al. · Neurology · 2012 · 224 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy

Maria Carmela Pera, Giorgia Coratti, Nicola Forcina et al. · BMC Neurology · 2017 · 221 citations · Full text

Medicine, Neurology, Rehabilitation Medicine +17