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Sangeetha Yoganathan

Showing results (61-70 of 89) with videos related to

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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.
Movement Disorders Clinical Practice|May 29, 2025
Clinical Phenotype and Neuroimaging Findings in Siblings with COX15 Deficiency: Case Report and Review of Previously Reported CasesHaya S AlFaris, Sangeetha Yoganathan, Marcus N Callister, et al.
HGG Advances|April 3, 2026
Broadening the phenotypic and molecular spectrum of PRS deficiency in femalesTamara Braid, Sydney Scholten, Sangeetha Yoganathan, 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.
Annals of Indian Academy of Neurology|October 10, 2022
Fumaric Aciduria: A Rare Cause of Refractory EpilepsySangeetha Yoganathan, Rangan Srinivasaraghavan, Madhan Kumar, et al.
Movement Disorders Clinical Practice|September 27, 2025
Reply: "Leigh Syndrome Due to the Variant c.1019T>C in COX15"Haya S AlFaris, Sangeetha Yoganathan, Marcus N Callister, et al.
Neurology|January 8, 2025
Cortical Myoclonus in an Adolescent Boy With a De Novo Pathogenic Variant in <i>NUS1</i> GeneSangeetha Yoganathan, Wei Kang Lim, Lindsey Vogt, et al.
Indian Dermatology Online Journal|March 26, 2021
The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control StudySirisha Varala, Renu George, Lydia Mathew, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 1, 2019
EEG lateralization and seizure outcome following peri-insular hemispherotomy for pediatric hemispheric epilepsyAnanth P Abraham, Maya Mary Thomas, Vivek Mathew, 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 9

Showing results (61-70 of 89) with videos related to

Sort By:
Pageof 9
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.
Movement Disorders Clinical Practice|May 29, 2025
Clinical Phenotype and Neuroimaging Findings in Siblings with COX15 Deficiency: Case Report and Review of Previously Reported CasesHaya S AlFaris, Sangeetha Yoganathan, Marcus N Callister, et al.
HGG Advances|April 3, 2026
Broadening the phenotypic and molecular spectrum of PRS deficiency in femalesTamara Braid, Sydney Scholten, Sangeetha Yoganathan, 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.
Annals of Indian Academy of Neurology|October 10, 2022
Fumaric Aciduria: A Rare Cause of Refractory EpilepsySangeetha Yoganathan, Rangan Srinivasaraghavan, Madhan Kumar, et al.
Movement Disorders Clinical Practice|September 27, 2025
Reply: "Leigh Syndrome Due to the Variant c.1019T>C in COX15"Haya S AlFaris, Sangeetha Yoganathan, Marcus N Callister, et al.
Neurology|January 8, 2025
Cortical Myoclonus in an Adolescent Boy With a De Novo Pathogenic Variant in <i>NUS1</i> GeneSangeetha Yoganathan, Wei Kang Lim, Lindsey Vogt, et al.
Indian Dermatology Online Journal|March 26, 2021
The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control StudySirisha Varala, Renu George, Lydia Mathew, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 1, 2019
EEG lateralization and seizure outcome following peri-insular hemispherotomy for pediatric hemispheric epilepsyAnanth P Abraham, Maya Mary Thomas, Vivek Mathew, 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 9