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Journal of Pediatric Neurosciences|April 21, 2018
A Tale of Treatable Infantile Neuroregression and Diagnostic Dilemma with Glutaric Aciduria Type ISangeetha Yoganathan, Mugil Varman, Samuel Philip Oommen, et al.
Indian Pediatrics|September 11, 2012
Growth and development profile of Indian children with Down syndromeBeena Koshy, Kirubakaran Navamani, Samuel Philip Oommen, et al.
Journal of Tropical Pediatrics|September 17, 2009
Development and dysmorphism in Joubert syndrome--short case series from IndiaBeena Koshy, Samuel Philip Oommen, Smitha Jasper, et al.
Indian Pediatrics|February 5, 2017
Dysmorphism in Non-Syndromic Autism: A Cross-Sectional StudySusan Mary Zachariah, Samuel Philip Oommen, Caroline Sanjeev Padankatti, et al.
Annals of Indian Academy of Neurology|February 15, 2020
Metabolic Stroke: A Novel Presentation in a Child with Succinic Semialdehyde Dehydrogenase DeficiencySangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, et al.
Neuropediatrics|October 18, 2024
Phenotype and Genotype of Children with ALS2 gene-Related DisorderSangeetha Yoganathan, Madhan Kumar, Rekha Aaron, et al.
Journal of Genetics|November 10, 2020
Methyl-CpG-binding protein 2 gene mutations and its association with epilepsy: a single centre study from the Indian subcontinentPayal Kamdar, Maya Thomas, Sangeetha Yoganathan, et al.
Pediatric Neurology|July 6, 2023
Childhood Neurological Disorders With Hyperhomocystinemia: A Case-Based ReviewSangeetha Yoganathan, Himani Bhasin, Divyani Garg, et al.
European Journal of Medical Genetics|July 25, 2021
Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinentSuneetha Susan Cleave Abraham, Sangeetha Yoganathan, Beena Koshy, et al.
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