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Acta Psychiatrica Scandinavica|August 22, 2009
Effects of a yoga breath intervention alone and in combination with an exposure therapy for post-traumatic stress disorder and depression in survivors of the 2004 South-East Asia tsunamiT Descilo, A Vedamurtachar, P L Gerbarg, et al.
Neurology India|October 28, 2020
Genetically Established Familial Amyloidotic Polyneuropathy from India: Narrating the Diagnostic "Odyssey" and a Mini ReviewMadhu Nagappa, Sanjib Sinha, Anita Mahadevan, et al.
The British Journal of Radiology|January 29, 2014
Bilateral hypertrophic olivary nucleus degeneration on magnetic resonance imaging in children with Leigh and Leigh-like syndromeP S Bindu, A B Taly, K Sonam, et al.
Journal of Neurogenetics|July 8, 2024
Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathyShivani Sharma, Anita Mahadevan, Gayathri Narayanappa, et al.
The American Journal of Tropical Medicine and Hygiene|September 3, 2020
Case Report: Chronic Fungal Meningitis Masquerading as Tubercular MeningitisNagabushan Hesarur, Doniparthi Venkata Seshagiri, Madhu Nagappa, et al.
Cytokine|April 29, 2018
Comprehensive cytokine profiling provides evidence for a multi-lineage Th responses in Guillain Barré SyndromeMonojit Debnath, Madhu Nagappa, Pinku Mani Talukdar, et al.
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.
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