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Narayanappa Gayathri

Showing results (21-30 of 45) with videos related to

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Journal of Clinical Neuromuscular Disease|November 22, 2014
Mitochondrial myopathy, cardiomyopathy, and pontine signal changes in an adult patient with isolated complex II deficiencyKothari Sonam, Parayil Sankaran Bindu, Arun B Taly, et al.
Journal of Neurochemistry|February 10, 2018
Mitochondrial dysfunction in human skeletal muscle biopsies of lipid storage disorderBandopadhyay Debashree, Manish Kumar, Thottethodi Subrahmanya Keshava Prasad, et al.
Annals of Indian Academy of Neurology|November 7, 2009
Epilepsia partialis continua in mitochondrial dysfunction: Interesting phenotypic and MRI observationsKalyani Karkare, Sanjib Sinha, Shivashankar Ravishankar, et al.
Plos One|July 24, 2014
Novel TCAP mutation c.32C>A causing limb girdle muscular dystrophy 2GAmirtharaj Francis, Balaraju Sunitha, Kandavalli Vinodh, et al.
Journal of Child Neurology|April 20, 2013
The "double panda" sign in Leigh diseaseKothari Sonam, P S Bindu, Narayanappa Gayathri, et al.
Neurology India|January 12, 2018
Natural history of a cohort of Duchenne muscular dystrophy children seen between 1998 and 2014: An observational study from South IndiaRavinder-Jeet Singh, Mahadevappa Manjunath, Veeramani Preethish-Kumar, et al.
Neuropediatrics|May 15, 2015
Clinical and Neuroimaging Features in Two Children with Mutations in the Mitochondrial ND5 GeneKothari Sonam, P S Bindu, Arun B Taly, et al.
The Journal of Biological Chemistry|November 14, 2013
Mitochondrial alterations and oxidative stress in an acute transient mouse model of muscle degeneration: implications for muscular dystrophy and related muscle pathologiesRenjini Ramadasan-Nair, Narayanappa Gayathri, Sudha Mishra, 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.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Journal of Clinical Neuromuscular Disease|November 22, 2014
Mitochondrial myopathy, cardiomyopathy, and pontine signal changes in an adult patient with isolated complex II deficiencyKothari Sonam, Parayil Sankaran Bindu, Arun B Taly, et al.
Journal of Neurochemistry|February 10, 2018
Mitochondrial dysfunction in human skeletal muscle biopsies of lipid storage disorderBandopadhyay Debashree, Manish Kumar, Thottethodi Subrahmanya Keshava Prasad, et al.
Annals of Indian Academy of Neurology|November 7, 2009
Epilepsia partialis continua in mitochondrial dysfunction: Interesting phenotypic and MRI observationsKalyani Karkare, Sanjib Sinha, Shivashankar Ravishankar, et al.
Plos One|July 24, 2014
Novel TCAP mutation c.32C>A causing limb girdle muscular dystrophy 2GAmirtharaj Francis, Balaraju Sunitha, Kandavalli Vinodh, et al.
Journal of Child Neurology|April 20, 2013
The "double panda" sign in Leigh diseaseKothari Sonam, P S Bindu, Narayanappa Gayathri, et al.
Neurology India|January 12, 2018
Natural history of a cohort of Duchenne muscular dystrophy children seen between 1998 and 2014: An observational study from South IndiaRavinder-Jeet Singh, Mahadevappa Manjunath, Veeramani Preethish-Kumar, et al.
Neuropediatrics|May 15, 2015
Clinical and Neuroimaging Features in Two Children with Mutations in the Mitochondrial ND5 GeneKothari Sonam, P S Bindu, Arun B Taly, et al.
The Journal of Biological Chemistry|November 14, 2013
Mitochondrial alterations and oxidative stress in an acute transient mouse model of muscle degeneration: implications for muscular dystrophy and related muscle pathologiesRenjini Ramadasan-Nair, Narayanappa Gayathri, Sudha Mishra, 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.
Pageof 5