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Journal of the Neurological Sciences|July 29, 2011
Mitochondrial neurogastrointestinal encephalopathy in an Indian family with possible manifesting carriers of heterozygous TYMP mutationAtchayaram Nalini, Narayanappa GayathriMitochondrion|September 30, 2021
Diagnosis of primary mitochondrial disorders -Emphasis on myopathological aspectsNarayanappa Gayathri, Sekar Deepha, Shivani SharmaAmerican Journal of Ophthalmology|April 30, 2003
Myopic strabismus fixus: a mitochondrial myopathy?Canjeevaram P Venkatesh, Narayanappa Gayathri, Krishnamoorthy R MurthyNeurology India|September 6, 2013
GNE myopathy in IndiaAtchayaram Nalini, Narayanappa Gayathri, Ischizo Nishino, et al.Annals of Indian Academy of Neurology|December 17, 2013
Bethlem myopathy: An autosomal dominant myopathy with flexion contractures, keloids, and follicular hyperkeratosisAralikatte Onkarappa Saroja, Karkal Ravishankar Naik, Atcharayam Nalini, et al.Analytical Chemistry|January 14, 2015
Raman spectroscopic studies on screening of myopathiesRekha Gautam, Sandeep Vanga, Aditi Madan, et al.Neurology India|January 21, 2014
New mutation of the desmin gene identified in an extended Indian pedigree presenting with distal myopathy and cardiac diseaseAtchayaram Nalini, Narayanappa Gayathri, Pascale Richard, et al.BMC Medical Genetics|June 15, 2017
MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from IndiaSekar Deepha, Seena Vengalil, Veeramani Preethish-Kumar, et al.Neurology India|July 21, 2010
Pattern recognition on brain magnetic resonance imaging in alpha dystroglycanopathiesParayil S Bindu, Narayanappa Gayathri, Rose D Bharath, et al.Journal of Neurochemistry|March 27, 2016
Muscle biopsies from human muscle diseases with myopathic pathology reveal common alterations in mitochondrial functionBalaraju Sunitha, Narayanappa Gayathri, Manish Kumar, et al.Pageof 5