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Journal of Pediatric Neurosciences|July 28, 2021
Siblings with Glutaric Aciduria Type 1 with Atypical Phenotype with Novel Pathogenic Variant in GCDH GeneVykuntaraju Kammasandra Gowda, Balamurugan Nagarajan, Varunvenkat M Srinivasan, et al.Journal of Pediatric Neurosciences|January 12, 2022
Familial Global Developmental Delay Secondary to β-MannosidosisVykuntaraju K Gowda, Balamurugan Nagarajan, Srividya G Suryanarayana, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 17, 2022
Nutritional Recovery Batwing Dystonia in Infantile Vitamin B12 DeficiencyPawan Kumar, Balamurugan Nagarajan, Sameer Vyas, et al.Journal of Pediatric Genetics|September 10, 2021
Profile of Indian Children with Childhood Ataxia and Central Nervous System Hypomyelination/Vanishing White Matter Disease: A Single Center Experience from Southern IndiaVykuntaraju K Gowda, Varunvenkat M Srinivasan, Balamurugan Nagarajan, et al.Journal of Pediatric Genetics|June 30, 2022
Rare Treatable Cause of Demyelinating Leukoencephalopathy That One Cannot Afford to MissVykuntaraju K Gowda, Sukanya Vignesh, Balamurugan Nagarajan, et al.Brain & Development|November 29, 2025
Neurological manifestations and clinical outcomes in pediatric Alexander disease: single-center cohort and identification of novel GFAP variantsRenu Suthar, Yashu Sharma, Arushi Gahlot Saini, et al.Epilepsia Open|August 16, 2023
Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from IndiaBalamurugan Nagarajan, Vykuntaraju K Gowda, Sangeetha Yoganathan, et al.Pageof 1