Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Current Opinion in Pediatrics|April 1, 2026
Treatment advances for Duchenne muscular dystrophyAlexander Zygmunt, Cuixia Tian
Seminars in Pediatric Neurology|December 8, 2023
Sleep in pediatric neuromuscular disordersJohn E Pascoe, Alexander Zygmunt, Zarmina Ehsan, et al.
Neuromuscular Disorders : NMD|March 27, 2026
From case to caution: hyponatremia in a patient with Duchenne muscular dystrophy on vamorolone and lessons for cliniciansChelsea Murphy, Nat Nasomyont, Cuixia Tian, et al.
Muscle & Nerve|September 18, 2024
The impact of genotype on age at loss of ambulation in individuals with Duchenne muscular dystrophy treated with corticosteroids: A single-center study of 555 patientsAlexander Zygmunt, Brenda Wong, David Moon, et al.
Pediatric Neurology|June 1, 2026
Fatal Fat Embolism Syndrome Without Recognized Fracture in Patients With Duchenne Muscular Dystrophy: Two Case ReportsCameron A Wade, Chet Villa, Larry B Goldstein, et al.
Pediatric Neurology|December 5, 2021
Lethal Pediatric Cerebral Vasculitis Triggered by Severe Acute Respiratory Syndrome Coronavirus 2Kelsey E Poisson, Alexander Zygmunt, Daniel Leino, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
Single nucleus RNA sequencing of juvenile dermatomyositis skeletal muscle identifies altered angiogenic signalingCasey O Swoboda, Carmy Forney, Cristofer Calvo, et al.
European Journal of Human Genetics : EJHG|June 14, 2025
Structural variation in nebulin and its impact on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletionsLydia Sagath, Kirsi Kiiski, Kireshnee Naidu, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletionsLydia Sagath, Kirsi Kiiski, Kireshnee Naidu, et al.
Pageof 1