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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.
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.
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