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Brain & Development
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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 Association
Karthik 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 entity
Prince 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 Disability
Vandana 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 therapy
Karthik Muthusamy, Sangeetha Yoganathan, Maya Mary Thomas, et al.
Neurology
|
December 15, 2021
<i>SGCE</i> Myoclonus-Dystonia: An Inherited Movement Disorder
Sangeetha Yoganathan, Madhan Kumar, Suvasini Sharma, et al.
Journal of Child Neurology
|
December 19, 2013
Isolated cerebellar involvement in vitamin B12 deficiency: a case report
Biswaroop 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 Study
Indumathy 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 Disorder
Sophy Korula, Sangeetha Yoganathan, Jeyanthi Peter, et al.
JCEM Case Reports
|
March 27, 2025
Diverse Phenotypes of Mitochondrial Disease With Varying Levels of Heteroplasmy
Rebecca John, Aaron Chapla, Geeta Chacko, et al.
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of 9
Search research articles
Search
Showing results (21-30 of 89) with videos related to
Sort By:
Page
of 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 Association
Karthik 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 entity
Prince 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 Disability
Vandana 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 therapy
Karthik Muthusamy, Sangeetha Yoganathan, Maya Mary Thomas, et al.
Neurology
|
December 15, 2021
<i>SGCE</i> Myoclonus-Dystonia: An Inherited Movement Disorder
Sangeetha Yoganathan, Madhan Kumar, Suvasini Sharma, et al.
Journal of Child Neurology
|
December 19, 2013
Isolated cerebellar involvement in vitamin B12 deficiency: a case report
Biswaroop 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 Study
Indumathy 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 Disorder
Sophy Korula, Sangeetha Yoganathan, Jeyanthi Peter, et al.
JCEM Case Reports
|
March 27, 2025
Diverse Phenotypes of Mitochondrial Disease With Varying Levels of Heteroplasmy
Rebecca John, Aaron Chapla, Geeta Chacko, et al.
Page
of 9