Meena AK - Search Results

1

Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India.

Khan NA, Govindaraj P, Soumittra N, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Taly AB, Bindu PS, Gayathri N, Thangaraj K. Khan NA, et al. Among authors: meena ak. Invest Ophthalmol Vis Sci. 2013 Jun 10;54(6):3999-4005. doi: 10.1167/iovs.13-11925. Invest Ophthalmol Vis Sci. 2013. PMID: 23674761

2

Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy.

Khan NA, Govindaraj P, Jyothi V, Meena AK, Thangaraj K. Khan NA, et al. Among authors: meena ak. Mol Vis. 2013 Jun 11;19:1282-9. Print 2013. Mol Vis. 2013. PMID: 23805034 Free PMC article.

3

Mitochondrial disorders: challenges in diagnosis & treatment.

Khan NA, Govindaraj P, Meena AK, Thangaraj K. Khan NA, et al. Among authors: meena ak. Indian J Med Res. 2015 Jan;141(1):13-26. doi: 10.4103/0971-5916.154489. Indian J Med Res. 2015. PMID: 25857492 Free PMC article. Review.

4

Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging.

Paramasivam A, Meena AK, Pedaparthi L, Jyothi V, Uppin MS, Jabeen SA, Sundaram C, Thangaraj K. Paramasivam A, et al. Among authors: meena ak. Mitochondrion. 2016 Jan;26:81-5. doi: 10.1016/j.mito.2015.12.006. Epub 2015 Dec 12. Mitochondrion. 2016. PMID: 26689116

5

Homozygous R627W mutations in POLG cause mitochondrial DNA depletion leading to encephalopathy, seizures and stroke-like episodes.

Paramasivam A, Venkatapathi C, Sandeep G, Meena AK, Uppin MS, Mohapatra S, Pitceathly RDS, Thangaraj K. Paramasivam A, et al. Among authors: meena ak. Mitochondrion. 2019 Sep;48:78-83. doi: 10.1016/j.mito.2019.08.003. Epub 2019 Aug 16. Mitochondrion. 2019. PMID: 31425757

6

MPV17 hepatocerebral mitochondrial DNA depletion syndrome presenting as acute flaccid paralysis - A case report.

Pyal A, Paramasivam A, Meena AK, Bhavana VB, Thangaraj K. Pyal A, et al. Among authors: meena ak. Mitochondrion. 2017 Nov;37:41-45. doi: 10.1016/j.mito.2017.06.006. Epub 2017 Jun 30. Mitochondrion. 2017. PMID: 28673863

7

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

Paramasivam A, Meena AK, Venkatapathi C, Pitceathly RDS, Thangaraj K. Paramasivam A, et al. Among authors: meena ak. J Mol Neurosci. 2020 Dec;70(12):1962-1965. doi: 10.1007/s12031-020-01595-8. Epub 2020 Jun 2. J Mol Neurosci. 2020. PMID: 32488845 Free PMC article.

8

Correction to: Novel Biallelic NSUN3 Variants Cause Early-Onset Mitochondrial Encephalomyopathy and Seizures.

Paramasivam A, Meena AK, Venkatapathi C, Pitceathly RDS, Thangaraj K. Paramasivam A, et al. Among authors: meena ak. J Mol Neurosci. 2020 Dec;70(12):1966. doi: 10.1007/s12031-020-01652-2. J Mol Neurosci. 2020. PMID: 32671698 Free PMC article.

9

Primary Cutaneous B-Cell Lymphoma in an Infant: A Rare Entity.

Sarkar R, Meena AK, Mendiratta V, Sonker S, Singh S. Sarkar R, et al. Among authors: meena ak. Indian J Dermatol. 2024 Mar-Apr;69(2):196-197. doi: 10.4103/ijd.ijd_1169_23. Epub 2024 Apr 29. Indian J Dermatol. 2024. PMID: 38841242 Free PMC article. No abstract available.

10

NDUFV1-Related Mitochondrial Complex-1 Disorders: A Retrospective Case Series and Literature Review.

Mahesan A, Choudhary PK, Kamila G, Rohil A, Meena AK, Kumar A, Jauhari P, Chakrabarty B, Gulati S. Mahesan A, et al. Among authors: meena ak. Pediatr Neurol. 2024 Jun;155:91-103. doi: 10.1016/j.pediatrneurol.2024.02.012. Epub 2024 Mar 6. Pediatr Neurol. 2024. PMID: 38626668 Review.

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