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Shwetha Chiplunkar

Showing results (1-10 of 17) with videos related to

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Journal of Child Neurology|March 18, 2020
Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene PanelBindu Parayil Sankaran, Madhu Nagappa, Shwetha Chiplunkar, et al.
Neurology|April 24, 2021
Child Neurology: Hereditary Folate MalabsorptionAkshata Huddar, Shwetha Chiplunkar, Madhu Nagappa, et al.
Neurology|October 24, 2018
Clinical Reasoning: West syndrome, pontocerebellar hypoplasia, and hypomyelination in a 6-month-old boyParayil Sankaran Bindu, Madhu Nagappa, Shwetha Chiplunkar, et al.
Neurology|December 28, 2016
Child Neurology: Sjögren-Larsson syndromeMadhu Nagappa, Parayil S Bindu, Shwetha Chiplunkar, et al.
Journal of Molecular Neuroscience : MN|January 20, 2021
Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from IndiaSekar Deepha, Periyasamy Govindaraj, Bindu Parayil Sankaran, et al.
Clinical Neurology and Neurosurgery|July 1, 2016
Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndromeV P Vandana, Parayil Sankaran Bindu, Kothari Sonam, et al.
Metabolic Brain Disease|June 17, 2016
Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1Shwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa, et al.
Mitochondrion|August 22, 2021
Serum fibroblast growth factor 21 and growth differentiation factor 15: Two sensitive biomarkers in the diagnosis of mitochondrial disordersAkshata Huddar, Periyasamy Govindaraj, Shwetha Chiplunkar, et al.
Clinical Neurology and Neurosurgery|September 8, 2016
Reply to Letter to the Editor: Hearing impairment in m.3243A>G carriers requires comprehensive work- and follow-upV P Vandana, Parayil Sankaran Bindu, Kothari Sonam, et al.
Multiple Sclerosis and Related Disorders|January 23, 2018
Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?Parayil Sankaran Bindu, Kothari Sonam, Shwetha Chiplunkar, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Journal of Child Neurology|March 18, 2020
Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene PanelBindu Parayil Sankaran, Madhu Nagappa, Shwetha Chiplunkar, et al.
Neurology|April 24, 2021
Child Neurology: Hereditary Folate MalabsorptionAkshata Huddar, Shwetha Chiplunkar, Madhu Nagappa, et al.
Neurology|October 24, 2018
Clinical Reasoning: West syndrome, pontocerebellar hypoplasia, and hypomyelination in a 6-month-old boyParayil Sankaran Bindu, Madhu Nagappa, Shwetha Chiplunkar, et al.
Neurology|December 28, 2016
Child Neurology: Sjögren-Larsson syndromeMadhu Nagappa, Parayil S Bindu, Shwetha Chiplunkar, et al.
Journal of Molecular Neuroscience : MN|January 20, 2021
Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from IndiaSekar Deepha, Periyasamy Govindaraj, Bindu Parayil Sankaran, et al.
Clinical Neurology and Neurosurgery|July 1, 2016
Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndromeV P Vandana, Parayil Sankaran Bindu, Kothari Sonam, et al.
Metabolic Brain Disease|June 17, 2016
Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1Shwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa, et al.
Mitochondrion|August 22, 2021
Serum fibroblast growth factor 21 and growth differentiation factor 15: Two sensitive biomarkers in the diagnosis of mitochondrial disordersAkshata Huddar, Periyasamy Govindaraj, Shwetha Chiplunkar, et al.
Clinical Neurology and Neurosurgery|September 8, 2016
Reply to Letter to the Editor: Hearing impairment in m.3243A>G carriers requires comprehensive work- and follow-upV P Vandana, Parayil Sankaran Bindu, Kothari Sonam, et al.
Multiple Sclerosis and Related Disorders|January 23, 2018
Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?Parayil Sankaran Bindu, Kothari Sonam, Shwetha Chiplunkar, et al.
Pageof 2