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Developmental Medicine and Child Neurology|September 21, 2019
Performance of Upper Limb module for Duchenne muscular dystrophyAnna G Mayhew, Giorgia Coratti, Elena Stacy Mazzone, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 19, 2006
Feeding problems and weight gain in Duchenne muscular dystrophyMarika Pane, Isabella Vasta, Sonia Messina, et al.Nature Genetics|May 1, 2012
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotypeMarcella Zollino, Daniela Orteschi, Marina Murdolo, et al.Pediatric Neurology|April 18, 2015
A diagnostic dilemma in a family with cystinuria type B resolved by muscle magnetic resonanceGuja Astrea, Iulia Munteanu, Denise Cassandrini, et al.Pediatric Neurology|March 24, 2009
Scale for evaluation of movement disorders in the first three years of lifeRoberta Battini, Andrea Guzzetta, Giuseppina Sgandurra, et al.Annals of Neurology|November 18, 2015
Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophyJerry R Mendell, Nathalie Goemans, Linda P Lowes, et al.Muscle & 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 Personalized Medicine|September 28, 2023
Hearing Impairment and Neuroimaging Results in Mitochondrial DiseasesGabriella Cadoni, Guido Primiano, Pasqualina M Picciotti, et al.Journal of Child Neurology|April 19, 2005
Epilepsy in shunted posthemorrhagic infantile hydrocephalus owing to pre- or perinatal intra- or periventricular hemorrhageDomenica Battaglia, Maria Grazia Pasca, Laura Cesarini, et al.Epilepsia|June 3, 2009
Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first caseChiara Veredice, Flaviana Bianco, Ilaria Contaldo, et al.Pageof 51