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Sangeetha Yoganathan

Showing results (21-30 of 89) with videos related to

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Brain & Development|November 26, 2015
"Eye of tiger sign" mimic in an adolescent boy with mitochondrial membrane protein associated neurodegeneration (MPAN)Sangeetha Yoganathan, Sniya Valsa Sudhakar, Maya Thomas, et al.
Journal of Child Neurology|September 13, 2014
Hypomyelination, Hypodontia, Hypogonadotropic Hypogonadism (4H) Syndrome With Vertebral Anomalies: A Novel AssociationKarthik Muthusamy, Sniya V Sudhakar, Sangeetha Yoganathan, et al.
Journal of Pediatric Rehabilitation Medicine|March 19, 2019
Status dystonicus: Diagnosis and management of a rare and challenging entityPrince Thakkar, Naveen B P, Sangeetha Yoganathan, et al.
Fetal and Pediatric Pathology|July 24, 2020
Utility of Chromosomal Microarray in Children with Unexplained Developmental Delay/Intellectual DisabilityVandana Kamath, Sangeetha Yoganathan, Maya Mary Thomas, et al.
Annals of Indian Academy of Neurology|March 7, 2015
Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapyKarthik Muthusamy, Sangeetha Yoganathan, Maya Mary Thomas, et al.
Neurology|December 15, 2021
<i>SGCE</i> Myoclonus-Dystonia: An Inherited Movement DisorderSangeetha Yoganathan, Madhan Kumar, Suvasini Sharma, et al.
Journal of Child Neurology|December 19, 2013
Isolated cerebellar involvement in vitamin B12 deficiency: a case reportBiswaroop Chakrabarty, Rachana Dubey, Sheffali Gulati, et al.
Annals of Indian Academy of Neurology|June 16, 2017
Predictors of Outcome in Children with Status Epilepticus during Resuscitation in Pediatric Emergency Department: A Retrospective Observational StudyIndumathy Santhanam, Sangeetha Yoganathan, V Akila Sivakumar, et al.
Annals of Indian Academy of Neurology|December 23, 2022
Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic DisorderSophy Korula, Sangeetha Yoganathan, Jeyanthi Peter, et al.
JCEM Case Reports|March 27, 2025
Diverse Phenotypes of Mitochondrial Disease With Varying Levels of HeteroplasmyRebecca John, Aaron Chapla, Geeta Chacko, et al.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 9
Brain & Development|November 26, 2015
"Eye of tiger sign" mimic in an adolescent boy with mitochondrial membrane protein associated neurodegeneration (MPAN)Sangeetha Yoganathan, Sniya Valsa Sudhakar, Maya Thomas, et al.
Journal of Child Neurology|September 13, 2014
Hypomyelination, Hypodontia, Hypogonadotropic Hypogonadism (4H) Syndrome With Vertebral Anomalies: A Novel AssociationKarthik Muthusamy, Sniya V Sudhakar, Sangeetha Yoganathan, et al.
Journal of Pediatric Rehabilitation Medicine|March 19, 2019
Status dystonicus: Diagnosis and management of a rare and challenging entityPrince Thakkar, Naveen B P, Sangeetha Yoganathan, et al.
Fetal and Pediatric Pathology|July 24, 2020
Utility of Chromosomal Microarray in Children with Unexplained Developmental Delay/Intellectual DisabilityVandana Kamath, Sangeetha Yoganathan, Maya Mary Thomas, et al.
Annals of Indian Academy of Neurology|March 7, 2015
Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapyKarthik Muthusamy, Sangeetha Yoganathan, Maya Mary Thomas, et al.
Neurology|December 15, 2021
<i>SGCE</i> Myoclonus-Dystonia: An Inherited Movement DisorderSangeetha Yoganathan, Madhan Kumar, Suvasini Sharma, et al.
Journal of Child Neurology|December 19, 2013
Isolated cerebellar involvement in vitamin B12 deficiency: a case reportBiswaroop Chakrabarty, Rachana Dubey, Sheffali Gulati, et al.
Annals of Indian Academy of Neurology|June 16, 2017
Predictors of Outcome in Children with Status Epilepticus during Resuscitation in Pediatric Emergency Department: A Retrospective Observational StudyIndumathy Santhanam, Sangeetha Yoganathan, V Akila Sivakumar, et al.
Annals of Indian Academy of Neurology|December 23, 2022
Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic DisorderSophy Korula, Sangeetha Yoganathan, Jeyanthi Peter, et al.
JCEM Case Reports|March 27, 2025
Diverse Phenotypes of Mitochondrial Disease With Varying Levels of HeteroplasmyRebecca John, Aaron Chapla, Geeta Chacko, et al.
Pageof 9