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American Journal of Ophthalmology|June 8, 2014
Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlationPiero Barboni, Giacomo Savini, Maria Lucia Cascavilla, et al.
Annals of Clinical and Translational Neurology|November 24, 2020
Risdiplam treatment has not led to retinal toxicity in patients with spinal muscular atrophyRobert C Sergott, Giulia M Amorelli, Giovanni Baranello, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|April 16, 2026
Vertebral fractures and muscle function in glucocorticoid-treated individuals with Duchenne muscular dystrophy: a cohort studyAnna Capasso, Chiara Arpaia, Chiara Panicucci, et al.
Journal of Neurology|May 12, 2023
Adult-onset leukodystrophy with vanishing white matter: a case series of 19 patientsChiara Benzoni, Marco Moscatelli, Laura Farina, et al.
Acta Diabetologica|June 21, 2022
Abnormalities of the oculomotor function in type 1 diabetes and diabetic neuropathyFrancesca D'Addio, Ida Pastore, Cristian Loretelli, et al.
European Journal of Neurology|October 19, 2022
Mutations in MYO9B are associated with Charcot-Marie-Tooth disease type 2 neuropathies and isolated optic atrophySilvia Cipriani, Marta Guerrero-Valero, Stefano Tozza, et al.
Annals of Neurology|March 29, 2020
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic NeuropathyLeonardo Caporali, Stefania Magri, Andrea Legati, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 14, 2020
Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA projectAnna Bersano, Emma Scelzo, Leonardo Pantoni, et al.
Prehospital and Disaster Medicine|September 7, 2023
Sudden-Onset Disaster Mass-Casualty Incident Response: A Modified Delphi Study on Triage, Prehospital Life Support, and ProcessesJoe Cuthbertson, Eric Weinstein, Jeffrey Michael Franc, et al.
Cell Reports. Medicine|January 25, 2024
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathySerena Jasmine Aleo, Valentina Del Dotto, Martina Romagnoli, et al.
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