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Children (Basel, Switzerland)|May 16, 2023
Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month StudyClaudia Brogna, Marika Pane, Giorgia Coratti, et al.
Early Human Development|July 23, 2013
Perceptual-motor abilities in pre-school preterm childrenPaola De Rose, Emilio Albamonte, Valentina Laganà, et al.
European Journal of Pediatrics|January 20, 2022
Body mass index in type 2 spinal muscular atrophy: a longitudinal studyGloria Ferrantini, Giorgia Coratti, Roberta Onesimo, et al.
European Journal of Pediatrics|August 29, 2024
Prognostic factors for tube feeding in type I SMA patients treated with disease-modifying therapies: a cohort studyMarika Pane, Giulia Stanca, Giorgia Coratti, et al.
The Journal of Pediatrics|February 10, 2020
Respiratory Needs in Patients with Type 1 Spinal Muscular Atrophy Treated with NusinersenValeria A Sansone, Alice Pirola, Emilio Albamonte, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 28, 2025
Patients on treatment with risdiplam in Italy: challenges in the interpretation of the real-world dataEmilio Albamonte, Adrea Lizio, Giorgia Coratti, et al.
Neuromuscular Disorders : NMD|October 21, 2019
Longitudinal natural history in young boys with Duchenne muscular dystrophyGiorgia Coratti, Claudia Brogna, Giulia Norcia, et al.
Annals of Clinical and Translational Neurology|February 15, 2022
Nusinersen efficacy data for 24-month in type 2 and 3 spinal muscular atrophyMarika Pane, Giorgia Coratti, Maria Carmela Pera, et al.
Annals of Clinical and Translational Neurology|February 6, 2021
Type I SMA "new natural history": long-term data in nusinersen-treated patientsMarika Pane, Giorgia Coratti, Valeria A Sansone, et al.
Neuromuscular Disorders : NMD|March 28, 2021
The nonsense mutation stop+4 model correlates with motor changes in Duchenne muscular dystrophyClaudia Brogna, Giorgia Coratti, Rachele Rossi, et al.
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