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Shwetha Chiplunkar

Showing results (11-20 of 17) with videos related to

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Brain & Development|September 7, 2016
Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) geneMadhu Nagappa, Parayil Sankaran Bindu, Shwetha Chiplunkar, et al.
Metabolic Brain Disease|May 4, 2017
Erratum to: Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiencyShwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa, et al.
Metabolic Brain Disease|April 5, 2017
Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiencyShwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa, et al.
Mitochondrion|November 10, 2016
Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South IndiaKothari Sonam, Parayil Sankaran Bindu, M M Srinivas Bharath, et al.
Mitochondrion|September 6, 2015
Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south IndiaParayil Sankaran Bindu, Hanumanthapura Arvinda, Arun B Taly, et al.
Mitochondrion|January 15, 2016
Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south IndiaParayil Sankaran Bindu, Chikanna Govindaraju, Kothari Sonam, et al.
Clinical Neurology and Neurosurgery|December 23, 2017
Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlationsParayil Sankaran Bindu, Kothari Sonam, Periyasamy Govindaraj, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Brain & Development|September 7, 2016
Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) geneMadhu Nagappa, Parayil Sankaran Bindu, Shwetha Chiplunkar, et al.
Metabolic Brain Disease|May 4, 2017
Erratum to: Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiencyShwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa, et al.
Metabolic Brain Disease|April 5, 2017
Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiencyShwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa, et al.
Mitochondrion|November 10, 2016
Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South IndiaKothari Sonam, Parayil Sankaran Bindu, M M Srinivas Bharath, et al.
Mitochondrion|September 6, 2015
Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south IndiaParayil Sankaran Bindu, Hanumanthapura Arvinda, Arun B Taly, et al.
Mitochondrion|January 15, 2016
Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south IndiaParayil Sankaran Bindu, Chikanna Govindaraju, Kothari Sonam, et al.
Clinical Neurology and Neurosurgery|December 23, 2017
Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlationsParayil Sankaran Bindu, Kothari Sonam, Periyasamy Govindaraj, et al.
Pageof 2