Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Muscle & Nerve|August 9, 2021
Age-related sensory neuropathy in patients with spinal muscular atrophy type 1Stefano Pro, Alberto Eugenio Tozzi, Adele D'Amico, et al.
Clinical Genetics|November 10, 2019
Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutationFabrizia Stregapede, Lorena Travaglini, Adriana P Rebelo, et al.
Parkinsonism & Related Disorders|January 8, 2025
Segmental brainstem myoclonus in ADCK3-Related ataxia: A novel phenomenon?Vito Luigi Colona, Giacomo Garone, Francesco Nicita, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 15, 2021
Acute strabismus in neurological emergencies of childhood: A retrospective, single-centre studyGiacomo Garone, Valentina Ferro, Marta Barbato, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 25, 2017
Bilateral loss of cortical SEPs predict severe MRI lesions in neonatal hypoxic ischemic encephalopathy treated with hypothermiaAgnese Suppiej, Ambra Cappellari, Giacomo Talenti, et al.
Journal of Clinical Medicine|July 24, 2021
Peripheral Nervous System Involvement in Non-Primary Pediatric Cancer: From Neurotoxicity to Possible EtiologiesStefano Pro, Luciana Vinti, Alessandra Boni, et al.
European Journal of Human Genetics : EJHG|May 17, 2022
"Atypical" Krabbe disease in two siblings harboring biallelic GALC mutations including a deep intronic variantFrancesco Nicita, Fabrizia Stregapede, Federica Deodato, et al.
Cancers|March 25, 2022
Short and Long-Term Toxicity in Pediatric Cancer Treatment: Central Nervous System DamageIside Alessi, Anna Maria Caroleo, Luca de Palma, et al.
Genes|April 27, 2024
Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From Mild to Severe FormsJacopo Sartorelli, Lorena Travaglini, Marina Macchiaiolo, et al.
Pageof 4