Angamuthu K. Meena

Novel Biallelic NSUN3 Variants Cause Early-Onset Mitochondrial Encephalomyopathy and Seizures

Paramasivam Arumugam, Angamuthu K. Meena, Challa Venkatapathi et al. · Journal of Molecular Neuroscience · 2020 · 43 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome

Sanjiban Chakrabarty, Periyasamy Govindaraj, Bindu Parayil Sankaran et al. · Journal of Neurology · 2021 · 38 citations · Full text

Life Sciences, Genetics, Neurology +17

Leber's Hereditary Optic Neuropathy–Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India

Nahid Khan, Periyasamy Govindaraj, Nagasamy Soumittra et al. · Investigative Ophthalmology & Visual Science · 2017 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Haplogroup Heterogeneity of LHON Patients Carrying the m.14484T>C Mutation in India

Nahid Khan, Periyasamy Govindaraj, Nagasamy Soumittra et al. · Investigative Ophthalmology & Visual Science · 2013 · 22 citations

Life Sciences, Genetics, Molecular Genetics +17

Pattern of Vascular Dementia in India: Study of Clinical Features, Imaging, and Vascular Mechanisms From a Hospital Dementia Registry

Suvarna Alladi, Subhash Kaul, Angamuthu K. Meena et al. · Journal of Stroke and Cerebrovascular Diseases · 2006 · 22 citations

Medicine, Geriatric Medicine, Neurology +17