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Neurourology and Urodynamics|December 4, 2019
The molecular effects of electrical stimulation on the muscle components of the urethra of female rats after trauma by vaginal distentionGisela R F Salerno, Maria A T Bortolini, Regina C T Gomes, et al.Gene Therapy|June 5, 2024
Gene replacement therapy for spinal muscular atrophy: safety and preliminary efficacy in a Brazilian cohortRodrigo Holanda Mendonça, Adriana Banzzatto Ortega, Ciro Matsui, et al.Lancet Regional Health. Americas|August 8, 2025
Safety and tolerability of onasemnogene abeparvovec for patients with spinal muscular atrophy weighing ≤17 kg and ≤24 months old from OFELIA, a phase 4, open-label, multicenter, non-randomised, interventional studyJonas Alex Saute, Javier Muntadas, Juliana Gurgel-Giannetti, et al.The Journal of Physiology|May 5, 2025
Integrated single-cell functional-proteomic profiling reveals a shift in myofibre specificity in human nemaline myopathy: A proof-of-principle studyRobert A E Seaborne, Roger Moreno-Justicia, Jenni Laitila, et al.Arquivos De Neuro-Psiquiatria|March 19, 2025
Brazilian Portuguese version of the revised upper-limb module: cross-cultural adaptation and validationMariana Cunha Artilheiro, Juliana Rodrigues Iannicelli, Graziela Jorge Polido, et al.Pediatric Neurology|March 21, 2016
A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic LevelsOsorio Abath Neto, Marina Rodrigues E Silva, Cristiane de Araújo Martins, et al.Pediatric Neurology|February 11, 2014
Congenital muscular dystrophy with dropped head linked to the LMNA gene in a Brazilian cohortLívia M A Pasqualin, Umbertina C Reed, Thais V M M Costa, et al.Journal of the Neurological Sciences|August 20, 2016
One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementiaAgessandro Abrahao, Osório Abath Neto, Fernando Kok, et al.Journal of Neurology|November 4, 2023
Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case seriesAlessia Pugliese, Adela Della Marina, Eduardo de Paula Estephan, et al.Arquivos De Neuro-Psiquiatria|June 23, 2026
Rhabdomyolysis: a narrative reviewCelia Harumi Tengan, Acary Souza Bulle Oliveira, Alzira Alves de Siqueira Carvalho, et al.Pageof 16