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Gayathri Narayanappa

Showing results (21-30 of 34) with videos related to

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Annals of Indian Academy of Neurology|December 30, 2015
Vocal cord palsy in a case of chronic progressive external ophthalmoplegiaSubasree Ramakrishnan, Ravi Yadav, Sikander Adwani, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|December 7, 2019
Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case reportBevinahalli N Nandeesh, Parayil Sankaran Bindu, Gayathri Narayanappa, et al.
Annals of Indian Academy of Neurology|July 5, 2021
Utility of Immunohistochemistry and Western Blot in Profiling Clinically Suspected Cases of Congenital Muscular DystrophyRadhika Mhatre, Deepha Sekar, Jessiena Ponmalar, et al.
Muscle & Nerve|November 13, 2014
Microsporidial polymyositis in human immunodeficiency virus-infected patients, a rare life-threatening opportunistic infection: clinical suspicion, diagnosis, and management in resource-limited settingsAtul K Patel, Ketan K Patel, Yasha T Chickabasaviah, et al.
Journal of Pediatric Genetics|December 1, 2021
Neuronal Ceroid Lipofuscinosis: Clinical and Laboratory Profile in Children from Tertiary Care Centre in South IndiaVykuntaraju K Gowda, Hemadri Vegda, Kiruthiga Sugumar, et al.
Neurology India|November 4, 2010
Tubular aggregate myopathy: a phenotypic spectrum and morphological studyAmrita Ghosh, Gayathri Narayanappa, Arun B Taly, et al.
Journal of Molecular Neuroscience : MN|January 30, 2021
A Dominant C150Y Mutation in FHL1 Induces Structural Alterations in LIM2 Domain Causing Protein Aggregation In Human and Drosophila Indirect Flight MusclesRashmi Santhoshkumar, Veeramani Preethish-Kumar, Kiran K Mangalaparthi, et al.
Indian Journal of Medical Microbiology|March 4, 2023
An ultrastructural and genomic study on the SARS-CoV-2 variant B.1.210 circulating during the first wave of COVID-19 pandemic in IndiaNarendra Kumar, Rashmi Santhoshkumar, Pramada Prasad, et al.
Journal of Molecular Neuroscience : MN|June 9, 2021
A Novel L1 Linker Mutation in DES Resulted in Total Absence of ProteinRashmi Santhoshkumar, Veeramani Preethish-Kumar, Kiran Polavarapu, 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.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Annals of Indian Academy of Neurology|December 30, 2015
Vocal cord palsy in a case of chronic progressive external ophthalmoplegiaSubasree Ramakrishnan, Ravi Yadav, Sikander Adwani, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|December 7, 2019
Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case reportBevinahalli N Nandeesh, Parayil Sankaran Bindu, Gayathri Narayanappa, et al.
Annals of Indian Academy of Neurology|July 5, 2021
Utility of Immunohistochemistry and Western Blot in Profiling Clinically Suspected Cases of Congenital Muscular DystrophyRadhika Mhatre, Deepha Sekar, Jessiena Ponmalar, et al.
Muscle & Nerve|November 13, 2014
Microsporidial polymyositis in human immunodeficiency virus-infected patients, a rare life-threatening opportunistic infection: clinical suspicion, diagnosis, and management in resource-limited settingsAtul K Patel, Ketan K Patel, Yasha T Chickabasaviah, et al.
Journal of Pediatric Genetics|December 1, 2021
Neuronal Ceroid Lipofuscinosis: Clinical and Laboratory Profile in Children from Tertiary Care Centre in South IndiaVykuntaraju K Gowda, Hemadri Vegda, Kiruthiga Sugumar, et al.
Neurology India|November 4, 2010
Tubular aggregate myopathy: a phenotypic spectrum and morphological studyAmrita Ghosh, Gayathri Narayanappa, Arun B Taly, et al.
Journal of Molecular Neuroscience : MN|January 30, 2021
A Dominant C150Y Mutation in FHL1 Induces Structural Alterations in LIM2 Domain Causing Protein Aggregation In Human and Drosophila Indirect Flight MusclesRashmi Santhoshkumar, Veeramani Preethish-Kumar, Kiran K Mangalaparthi, et al.
Indian Journal of Medical Microbiology|March 4, 2023
An ultrastructural and genomic study on the SARS-CoV-2 variant B.1.210 circulating during the first wave of COVID-19 pandemic in IndiaNarendra Kumar, Rashmi Santhoshkumar, Pramada Prasad, et al.
Journal of Molecular Neuroscience : MN|June 9, 2021
A Novel L1 Linker Mutation in DES Resulted in Total Absence of ProteinRashmi Santhoshkumar, Veeramani Preethish-Kumar, Kiran Polavarapu, 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.
Pageof 4