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Sangeetha Yoganathan

Showing results (81-90 of 89) with videos related to

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Journal of Inherited Metabolic Disease|May 5, 2025
Consensus of Expert Opinion for the Diagnosis and Management of Hypermanganesaemia With Dystonia 1 and 2Sherry Fang, Peter T Clayton, Divyani Garg, et al.
Movement Disorders Clinical Practice|May 12, 2026
Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case-Series and Literature ReviewSangeetha Yoganathan, Laura Tochen, Jacky Ganguly, et al.
Neurology. Genetics|May 22, 2025
<i>PRRT</i> <i>2</i>-Related Epilepsy: From Self-Limited Infantile Epilepsy to Atypical Epilepsy PhenotypesMadeline Komar, Jashanpreet Sidhu, Jiju Joseph, 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.
Movement Disorders Clinical Practice|October 17, 2022
Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian ChildrenDivyani Garg, Sangeetha Yoganathan, Uzma Shamim, et al.
Epilepsia|March 14, 2020
KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric casesFelippe Borlot, Ahmed Abushama, Nadine Morrison-Levy, et al.
Epilepsia|January 17, 2024
KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literatureSangeetha Yoganathan, Robyn Whitney, Maya Thomas, et al.
Nature Communications|May 28, 2016
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystoniaKarin Tuschl, Esther Meyer, Leonardo E Valdivia, et al.
Neurology. Genetics|November 18, 2021
<i>PURA-</i>Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic SpectrumKatrine M Johannesen, Elena Gardella, Cathrine E Gjerulfsen, et al.
Pageof 9

Showing results (81-90 of 89) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 89 results.
Journal of Inherited Metabolic Disease|May 5, 2025
Consensus of Expert Opinion for the Diagnosis and Management of Hypermanganesaemia With Dystonia 1 and 2Sherry Fang, Peter T Clayton, Divyani Garg, et al.
Movement Disorders Clinical Practice|May 12, 2026
Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case-Series and Literature ReviewSangeetha Yoganathan, Laura Tochen, Jacky Ganguly, et al.
Neurology. Genetics|May 22, 2025
<i>PRRT</i> <i>2</i>-Related Epilepsy: From Self-Limited Infantile Epilepsy to Atypical Epilepsy PhenotypesMadeline Komar, Jashanpreet Sidhu, Jiju Joseph, 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.
Movement Disorders Clinical Practice|October 17, 2022
Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian ChildrenDivyani Garg, Sangeetha Yoganathan, Uzma Shamim, et al.
Epilepsia|March 14, 2020
KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric casesFelippe Borlot, Ahmed Abushama, Nadine Morrison-Levy, et al.
Epilepsia|January 17, 2024
KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literatureSangeetha Yoganathan, Robyn Whitney, Maya Thomas, et al.
Nature Communications|May 28, 2016
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystoniaKarin Tuschl, Esther Meyer, Leonardo E Valdivia, et al.
Neurology. Genetics|November 18, 2021
<i>PURA-</i>Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic SpectrumKatrine M Johannesen, Elena Gardella, Cathrine E Gjerulfsen, et al.
Pageof 9