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Maya Thomas

Showing results (51-60 of 72) with videos related to

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Indian Pediatrics|April 8, 2024
Acute Encephalitis Syndrome in Children and Adolescents: A Five-Year Descriptive Study From South IndiaBetsy Rebecca, Maya Thomas, Asha Mary Abraham, et al.
Annals of Indian Academy of Neurology|July 5, 2021
Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental DisorderSangeetha Yoganathan, Rangan Srinivasaraghavan, Mahalakshmi Chandran, et al.
BMC Health Services Research|March 25, 2025
Functionality and performance of COVID-19 taskforces in response to the pandemic in UgandaDavid Musoke, Micheal Jonga, Gloria Kisakye Ndagire, et al.
Neuropediatrics|October 18, 2024
Phenotype and Genotype of Children with ALS2 gene-Related DisorderSangeetha Yoganathan, Madhan Kumar, Rekha Aaron, et al.
Annals of Indian Academy of Neurology|July 2, 2020
Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic DisorderSangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, et al.
Indian Journal of Ophthalmology|July 6, 2022
Eye signs in a child with <i>ROBO3</i> gene mutationSangeetha Yoganathan, Madhan Kumar, Mukul Malhotra, et al.
Frontiers in Neurology|August 11, 2023
Adult-onset leukodystrophies: a practical guide, recent treatment updates, and future directionsKarthik Muthusamy, Ajith Sivadasan, Luke Dixon, et al.
Annals of Indian Academy of Neurology|October 10, 2022
Fumaric Aciduria: A Rare Cause of Refractory EpilepsySangeetha Yoganathan, Rangan Srinivasaraghavan, Madhan Kumar, et al.
Scientific Reports|May 16, 2026
Prevalence and carrier frequency of Canavan disease in a South Indian community with implications for research and public healthRekha Aaron, Aaron Chapla, M Jayaprabha, 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.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
Indian Pediatrics|April 8, 2024
Acute Encephalitis Syndrome in Children and Adolescents: A Five-Year Descriptive Study From South IndiaBetsy Rebecca, Maya Thomas, Asha Mary Abraham, et al.
Annals of Indian Academy of Neurology|July 5, 2021
Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental DisorderSangeetha Yoganathan, Rangan Srinivasaraghavan, Mahalakshmi Chandran, et al.
BMC Health Services Research|March 25, 2025
Functionality and performance of COVID-19 taskforces in response to the pandemic in UgandaDavid Musoke, Micheal Jonga, Gloria Kisakye Ndagire, et al.
Neuropediatrics|October 18, 2024
Phenotype and Genotype of Children with ALS2 gene-Related DisorderSangeetha Yoganathan, Madhan Kumar, Rekha Aaron, et al.
Annals of Indian Academy of Neurology|July 2, 2020
Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic DisorderSangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, et al.
Indian Journal of Ophthalmology|July 6, 2022
Eye signs in a child with <i>ROBO3</i> gene mutationSangeetha Yoganathan, Madhan Kumar, Mukul Malhotra, et al.
Frontiers in Neurology|August 11, 2023
Adult-onset leukodystrophies: a practical guide, recent treatment updates, and future directionsKarthik Muthusamy, Ajith Sivadasan, Luke Dixon, et al.
Annals of Indian Academy of Neurology|October 10, 2022
Fumaric Aciduria: A Rare Cause of Refractory EpilepsySangeetha Yoganathan, Rangan Srinivasaraghavan, Madhan Kumar, et al.
Scientific Reports|May 16, 2026
Prevalence and carrier frequency of Canavan disease in a South Indian community with implications for research and public healthRekha Aaron, Aaron Chapla, M Jayaprabha, 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.
Pageof 8