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Page 1
Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.
J Clin Med. 2017 May 5;6(5):52. doi: 10.3390/jcm6050052.
J Clin Med. 2017.
PMID: 28475111
Free PMC article.
Review.
Brown-Vialetto-Van Laere and Fazio-Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance.
Gayathri S, Gowda VK, Udhayabanu T, O'Callaghan B, Efthymiou S, Varalakshmi P, Benakappa N, Houlden H, Ashokkumar B.
Gayathri S, et al. Among authors: udhayabanu t.
Eur J Neurol. 2021 Mar;28(3):945-954. doi: 10.1111/ene.14682. Epub 2021 Jan 5.
Eur J Neurol. 2021.
PMID: 33325104
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Fazio-Londe syndrome in siblings from India with different phenotypes.
Gowda VK, Udhayabanu T, Varalakshmi P, Srinivasan VM, Ashokkumar B.
Gowda VK, et al. Among authors: udhayabanu t.
Brain Dev. 2018 Aug;40(7):582-586. doi: 10.1016/j.braindev.2018.02.010. Epub 2018 Mar 2.
Brain Dev. 2018.
PMID: 29501408
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Adaptive regulation of riboflavin transport in heart: effect of dietary riboflavin deficiency in cardiovascular pathogenesis.
Udhayabanu T, Karthi S, Mahesh A, Varalakshmi P, Manole A, Houlden H, Ashokkumar B.
Udhayabanu T, et al.
Mol Cell Biochem. 2018 Mar;440(1-2):147-156. doi: 10.1007/s11010-017-3163-1. Epub 2017 Aug 23.
Mol Cell Biochem. 2018.
PMID: 28836047
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SLC52A2 [p.P141T] and SLC52A3 [p.N21S] causing Brown-Vialetto-Van Laere Syndrome in an Indian patient: First genetically proven case with mutations in two riboflavin transporters.
Udhayabanu T, Subramanian VS, Teafatiller T, Gowda VK, Raghavan VS, Varalakshmi P, Said HM, Ashokkumar B.
Udhayabanu T, et al.
Clin Chim Acta. 2016 Nov 1;462:210-214. doi: 10.1016/j.cca.2016.09.022. Epub 2016 Oct 1.
Clin Chim Acta. 2016.
PMID: 27702554
Free PMC article.
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