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Investigative Ophthalmology & Visual Science|May 16, 2013
Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in IndiaNahid Akhtar Khan, Periyasamy Govindaraj, Nagasamy Soumittra, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 29, 2020
Evidence of altered Th17 pathway signatures in the cerebrospinal fluid of patients with Guillain Barré SyndromeMonojit Debnath, Madhu Nagappa, Debprasad Dutta, et al.
Multiple Sclerosis and Related Disorders|January 23, 2018
Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?Parayil Sankaran Bindu, Kothari Sonam, Shwetha Chiplunkar, et al.
Brain & Development|September 7, 2016
Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) geneMadhu Nagappa, Parayil Sankaran Bindu, Shwetha Chiplunkar, et al.
Journal of Neuroimmunology|September 11, 2018
Th17 pathway signatures in a large Indian cohort of Guillain Barré syndromeMonojit Debnath, Madhu Nagappa, Manjula Subbanna, et al.
European Journal of Neurology|March 24, 2022
Role of altered IL-33/ST2 immune axis in the immunobiology of Guillain-Barré syndromePraveen P Sharma, Doniparthi V Seshagiri, Madhu Nagappa, et al.
Investigative Ophthalmology & Visual Science|August 3, 2017
Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in IndiaNahid Akhtar Khan, Periyasamy Govindaraj, Nagasamy Soumittra, et al.
Metabolic Brain Disease|April 5, 2017
Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiencyShwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa, et al.
Annals of Indian Academy of Neurology|August 27, 2021
Vogt-Koyanagi-Harada Syndrome - A Neurologist's PerspectiveSumanth Shivaram, Madhu Nagappa, Doniparthi V Seshagiri, et al.
Mitochondrion|November 10, 2016
Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South IndiaKothari Sonam, Parayil Sankaran Bindu, M M Srinivas Bharath, et al.
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