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Metabolic Brain Disease|October 24, 2018
A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemiaSarah Silverstein, Aravindhan Veerapandiyan, Caroline Hayes-Rosen, et al.Pediatric Neurology|November 26, 2011
Two patients with an anti-N-methyl-D-aspartate receptor antibody syndrome-like presentation and negative results of testing for autoantibodiesRikin Shah, Aravindhan Veerapandiyan, Sara Winchester, et al.Annals of the Child Neurology Society|August 7, 2026
Charcot-Marie-Tooth disease in childrenEzgi Saylam, Praveen Kumar Ramani, Ruthwik Duvuru, et al.European Journal of Medical Genetics|October 5, 2010
Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutationAravindhan Veerapandiyan, Ivan Kingyue Chinn, Kelly Schoch, et al.The Laryngoscope|February 10, 2011
The role of cephalometry in assessing velopharyngeal dysfunction in velocardiofacial syndromeAravindhan Veerapandiyan, David Blalock, Srija Ghosh, et al.Journal of Comparative Effectiveness Research|July 18, 2025
Real-world phosphorodiamidate morpholino oligomer treatment patterns in Duchenne muscular dystrophy: a claims-based analysisShannon Grabich, Brian Ung, Aalok Nadkar, et al.Child Neurology Open|September 1, 2017
A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene: Clinical Course and Response to RiboflavinVenkatraman Thulasi, Aravindhan Veerapandiyan, Beth A Pletcher, et al.Pediatric Neurology|April 13, 2026
Health Care Providers' Practices and Perspectives on Discussing Life Expectancy With Patients With Duchenne Muscular Dystrophy and Their CaregiversTy Copeland, Lauren Treat, Ruthwik Duvuru, et al.Journal of Child Neurology|July 11, 2018
Use of Head Computed Tomography (CT) in the Pediatric Emergency Department in Evaluation of Children With New-Onset Afebrile SeizureAravindhan Veerapandiyan, Akilandeswari Aravindhan, James Huynh Takahashi, et al.Muscle & Nerve|April 20, 2021
Recovery of foot drop in chronic inflammatory demyelinating polyneuropathy (CIDP)Dinushi Weerasinghe, Aravindhan Veerapandiyan, Michael Stanton, et al.Pageof 6