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Frontiers in Pediatrics|November 14, 2024
Case Report: Ocular paroxysmal non-epileptic events as the presenting sign of celiac disease in children: a case seriesAlice Monzani, Giulia Genoni, Amanda Papa, et al.European Journal of Medical Genetics|September 4, 2013
Dravet phenotype in a subject with a der(4)t(4;8)(p16.3;p23.3) without the involvement of the LETM1 geneBaran Bayindir, Elena Piazza, Erika Della Mina, et al.Journal of Child Neurology|August 14, 2023
Acquired Demyelinating Syndromes of the Central Nervous System in Children: The Importance of Regular Follow-up in the First Year After OnsetCarlotta Canavese, Irene Favole, Rossella D'Alessandro, et al.Seizure|September 19, 2025
Prediction of evolution to epilepsy or genetic epilepsy with febrile seizures plus (GEFS+) in children presenting with febrile seizures: a retrospective multicenter longitudinal studyPietro Baso, Silvia Masnada, Monica Maria Lodi, et al.Nutrients|January 25, 2025
Amino Acid Patterns in Children with Autistic Spectrum Disorder: A Preliminary Biochemical EvaluationSimona Ferraro, Laura Saielli, Davide Biganzoli, et al.European Journal of Human Genetics : EJHG|May 23, 2014
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platformErika Della Mina, Roberto Ciccone, Francesca Brustia, et al.Neuromuscular Disorders : NMD|January 21, 2014
Reliability of the Performance of Upper Limb assessment in Duchenne muscular dystrophyMarika Pane, Elena S Mazzone, Lavinia Fanelli, et al.Plos Currents|February 3, 2015
The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boysMarika Pane, Elena Stacy Mazzone, Serena Sivo, et al.Pageof 1