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Gayathri Narayanappa

Showing results (11-20 of 34) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 8, 2008
Autosomal recessive tubular aggregate myopathy in an Indian familyLekha Pandit, Gayathri Narayanappa, Irruvathur Gopalakrishna Bhat, et al.
Journal of Pediatric Neurosciences|February 3, 2021
Macrophagic Myofasciitis: A Report of Two South Indian InfantsVykuntaraju K Gowda, Varunvenkat M Srinivasan, Yasha Muthane, et al.
Neurology India|November 23, 2013
Mucolipidosis and progressive myoclonus epilepsy: a distinctive phenotypeRamshekhar N Menon, Sujith Jagtap, Ravindra Thakkar, et al.
Journal of Neuromuscular Diseases|January 15, 2023
MLIP-Associated Myopathy: A Case Report and Review of the LiteratureFatema Al Amrani, Khalid Al-Thihli, Gayathri Narayanappa, et al.
Intervirology|June 29, 2018
Chikungunya Virus Interacts with Heat Shock Cognate 70 Protein to Facilitate Its Entry into Mosquito Cell LineAyushman Ghosh, Anita Desai, Vasanthapuram Ravi, et al.
Neurology India|March 15, 2017
Young onset Parkinsonism in a patient with familial central core diseaseP Samuel Joseph, D M Syam Krishnan, Gayathri Narayanappa, et al.
Disease Models & Mechanisms|April 19, 2018
Sporadic amyotrophic lateral sclerosis (SALS) - skeletal muscle response to cerebrospinal fluid from SALS patients in a rat modelShruthi Shanmukha, Gayathri Narayanappa, Atchayaram Nalini, et al.
Journal of Pediatric Neurosciences|May 22, 2020
Myelopathy in Two Brothers with Respiratory Chain Disorder-Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported AssociationSadanandavalli Retnaswami Chandra, Hansashree Padmanabha, Manisha Gupta, et al.
Journal of Pediatric Neurosciences|October 2, 2018
Lipid Storage Myopathy with Ketonuria: A Case of Fatty Acid Oxidation-Related Myopathy and Encephalopathy due to Multiple Acyl-CoA Dehydrogenase DeficiencySadanandavalli R Chandra, Rita Christopher, Gayathri Narayanappa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Clinical features of adult GM1 gangliosidosis: report of three Indian patients and review of 40 casesUday Muthane, Yasha Chickabasaviah, Chris Kaneski, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 8, 2008
Autosomal recessive tubular aggregate myopathy in an Indian familyLekha Pandit, Gayathri Narayanappa, Irruvathur Gopalakrishna Bhat, et al.
Journal of Pediatric Neurosciences|February 3, 2021
Macrophagic Myofasciitis: A Report of Two South Indian InfantsVykuntaraju K Gowda, Varunvenkat M Srinivasan, Yasha Muthane, et al.
Neurology India|November 23, 2013
Mucolipidosis and progressive myoclonus epilepsy: a distinctive phenotypeRamshekhar N Menon, Sujith Jagtap, Ravindra Thakkar, et al.
Journal of Neuromuscular Diseases|January 15, 2023
MLIP-Associated Myopathy: A Case Report and Review of the LiteratureFatema Al Amrani, Khalid Al-Thihli, Gayathri Narayanappa, et al.
Intervirology|June 29, 2018
Chikungunya Virus Interacts with Heat Shock Cognate 70 Protein to Facilitate Its Entry into Mosquito Cell LineAyushman Ghosh, Anita Desai, Vasanthapuram Ravi, et al.
Neurology India|March 15, 2017
Young onset Parkinsonism in a patient with familial central core diseaseP Samuel Joseph, D M Syam Krishnan, Gayathri Narayanappa, et al.
Disease Models & Mechanisms|April 19, 2018
Sporadic amyotrophic lateral sclerosis (SALS) - skeletal muscle response to cerebrospinal fluid from SALS patients in a rat modelShruthi Shanmukha, Gayathri Narayanappa, Atchayaram Nalini, et al.
Journal of Pediatric Neurosciences|May 22, 2020
Myelopathy in Two Brothers with Respiratory Chain Disorder-Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported AssociationSadanandavalli Retnaswami Chandra, Hansashree Padmanabha, Manisha Gupta, et al.
Journal of Pediatric Neurosciences|October 2, 2018
Lipid Storage Myopathy with Ketonuria: A Case of Fatty Acid Oxidation-Related Myopathy and Encephalopathy due to Multiple Acyl-CoA Dehydrogenase DeficiencySadanandavalli R Chandra, Rita Christopher, Gayathri Narayanappa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Clinical features of adult GM1 gangliosidosis: report of three Indian patients and review of 40 casesUday Muthane, Yasha Chickabasaviah, Chris Kaneski, et al.
Pageof 4