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Insights from Magnetic Evoked Field Analysis in Patients with Wilson's Disease.
Aruna R, Mariyappa N, Sinha S, Nagappa M, Velmurugan J, Saini J, Bindu PS, Mathuranath PS, Thennarasu K, Satishchandra P, Taly AB. Aruna R, et al. Among authors: mathuranath ps. Neurol India. 2022 Sep-Oct;70(5):1963-1970. doi: 10.4103/0028-3886.359230. Neurol India. 2022. PMID: 36352595 Free article.
Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene.
Nagappa M, Bindu PS, Chiplunkar S, Govindaraj P, Narayanappa G, Krishnan A, Bharath MM, Swaminathan A, Saini J, Arvinda HR, Sinha S, Mathuranath PS, Taly AB. Nagappa M, et al. Among authors: mathuranath ps. Brain Dev. 2017 Feb;39(2):161-165. doi: 10.1016/j.braindev.2016.08.005. Epub 2016 Sep 3. Brain Dev. 2017. PMID: 27596361
Fatal Morvan Syndrome Associated With Myasthenia Gravis.
Nagappa M, Mahadevan A, Sinha S, Bindu PS, Mathuranath PS, Bineesh C, Bharath RD, Taly AB. Nagappa M, et al. Among authors: mathuranath ps. Neurologist. 2017 Jan;22(1):29-33. doi: 10.1097/NRL.0000000000000097. Neurologist. 2017. PMID: 28009770
Child Neurology: Sjögren-Larsson syndrome.
Nagappa M, Bindu PS, Chiplunkar S, Gupta N, Sinha S, Mathuranath PS, Bharath RD, Taly AB. Nagappa M, et al. Among authors: mathuranath ps. Neurology. 2017 Jan 3;88(1):e1-e4. doi: 10.1212/WNL.0000000000003456. Neurology. 2017. PMID: 28025403 No abstract available.
Erratum to: Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency.
Chiplunkar S, Bindu PS, Nagappa M, Panikulam BB, Arvinda HR, Govindaraj P, Srinivas Bharath MM, Gayathri N, Jessiena Ponmalar JN, Mathuranath PS, Sinha S, Taly AB. Chiplunkar S, et al. Among authors: mathuranath ps. Metab Brain Dis. 2017 Aug;32(4):971. doi: 10.1007/s11011-017-0018-0. Metab Brain Dis. 2017. PMID: 28466389 No abstract available.
86 results