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Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency.
Metab Brain Dis. 2017 Aug;32(4):967-970. doi: 10.1007/s11011-017-0005-5. Epub 2017 Apr 3.
Metab Brain Dis. 2017.
PMID: 28374236
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: jessiena ponmalar jn.
Metab Brain Dis. 2017 Aug;32(4):971. doi: 10.1007/s11011-017-0018-0.
Metab Brain Dis. 2017.
PMID: 28466389
No abstract available.
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Child Neurology: Ethylmalonic encephalopathy.
Govindaraj P, Parayil Sankaran B, Nagappa M, Arvinda HR, Deepha S, Jessiena Ponmalar JN, Sinha S, Gayathri N, Taly AB.
Govindaraj P, et al. Among authors: jessiena ponmalar jn.
Neurology. 2020 Mar 24;94(12):e1336-e1339. doi: 10.1212/WNL.0000000000009144. Epub 2020 Feb 28.
Neurology. 2020.
PMID: 32111695
No abstract available.
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Serum fibroblast growth factor 21 and growth differentiation factor 15: Two sensitive biomarkers in the diagnosis of mitochondrial disorders.
Huddar A, Govindaraj P, Chiplunkar S, Deepha S, Jessiena Ponmalar JN, Philip M, Nagappa M, Narayanappa G, Mahadevan A, Sinha S, Taly AB, Parayil Sankaran B.
Huddar A, et al. Among authors: jessiena ponmalar jn.
Mitochondrion. 2021 Sep;60:170-177. doi: 10.1016/j.mito.2021.08.011. Epub 2021 Aug 19.
Mitochondrion. 2021.
PMID: 34419687
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