Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Narayanappa Gayathri

Showing results (11-20 of 45) with videos related to

Pageof 5
Sort By:
Annals of Indian Academy of Neurology|December 30, 2015
An uncommon cause of bifacial weakness and non-length-dependent demyelinating neuropathyMadhu Nagappa, Arun B Taly, Anita Mahadevan, et al.
Neurology India|August 5, 2015
A prospective study on the immunophenotypic characterization of limb girdle muscular dystrophies 2 in IndiaAtchayaram Nalini, Kiran Polavarapu, Balaraju Sunitha, et al.
Annals of Indian Academy of Neurology|September 4, 2010
Familial amyloidotic polyneuropathy with muscle, vitreous, leptomeningeal, and cardiac involvement: phenotypic, pathological, and MRI descriptionD K Prashantha, Arun B Taly, Sanjib Sinha, et al.
Journal of Child Neurology|September 13, 2014
Giant axonal neuropathyKadambari Vijaykumar, Parayil Sankaran Bindu, Arun B Taly, et al.
Scientific Reports|January 16, 2021
Inhibition of mitochondrial complex II in neuronal cells triggers unique pathways culminating in autophagy with implications for neurodegenerationSathyanarayanan Ranganayaki, Neema Jamshidi, Mohamad Aiyaz, et al.
Molecular Vision|August 10, 2012
Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophySaketh Kapoor, Parayil Sankaran Bindu, Arun B Taly, et al.
Mitochondrion|February 27, 2021
Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters the mitochondrial function in human skeletal muscle proteomeGajanan Sathe, Sekar Deepha, Narayanappa Gayathri, et al.
Journal of Child Neurology|December 17, 2008
A variant form of mucolipidosis IV: report on 4 patients from the Indian subcontinentParayil Sankaran Bindu, Narayanappa Gayathri, Thagadur C Yasha, et al.
Neuromuscular Disorders : NMD|September 21, 2017
Fatty acid oxidation defects presenting as primary myopathy and prominent dropped head syndromeSeena Vengalil, Veeramani Preethish-Kumar, Kiran Polavarapu, et al.
Brain & Development|August 28, 2012
Electro-clinical features and magnetic resonance imaging correlates in Menkes diseaseParayil Sankaran Bindu, Arun B Taly, Sonam Kothari, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Annals of Indian Academy of Neurology|December 30, 2015
An uncommon cause of bifacial weakness and non-length-dependent demyelinating neuropathyMadhu Nagappa, Arun B Taly, Anita Mahadevan, et al.
Neurology India|August 5, 2015
A prospective study on the immunophenotypic characterization of limb girdle muscular dystrophies 2 in IndiaAtchayaram Nalini, Kiran Polavarapu, Balaraju Sunitha, et al.
Annals of Indian Academy of Neurology|September 4, 2010
Familial amyloidotic polyneuropathy with muscle, vitreous, leptomeningeal, and cardiac involvement: phenotypic, pathological, and MRI descriptionD K Prashantha, Arun B Taly, Sanjib Sinha, et al.
Journal of Child Neurology|September 13, 2014
Giant axonal neuropathyKadambari Vijaykumar, Parayil Sankaran Bindu, Arun B Taly, et al.
Scientific Reports|January 16, 2021
Inhibition of mitochondrial complex II in neuronal cells triggers unique pathways culminating in autophagy with implications for neurodegenerationSathyanarayanan Ranganayaki, Neema Jamshidi, Mohamad Aiyaz, et al.
Molecular Vision|August 10, 2012
Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophySaketh Kapoor, Parayil Sankaran Bindu, Arun B Taly, et al.
Mitochondrion|February 27, 2021
Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters the mitochondrial function in human skeletal muscle proteomeGajanan Sathe, Sekar Deepha, Narayanappa Gayathri, et al.
Journal of Child Neurology|December 17, 2008
A variant form of mucolipidosis IV: report on 4 patients from the Indian subcontinentParayil Sankaran Bindu, Narayanappa Gayathri, Thagadur C Yasha, et al.
Neuromuscular Disorders : NMD|September 21, 2017
Fatty acid oxidation defects presenting as primary myopathy and prominent dropped head syndromeSeena Vengalil, Veeramani Preethish-Kumar, Kiran Polavarapu, et al.
Brain & Development|August 28, 2012
Electro-clinical features and magnetic resonance imaging correlates in Menkes diseaseParayil Sankaran Bindu, Arun B Taly, Sonam Kothari, et al.
Pageof 5