Tamilarasan Udhayabanu

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

Tamilarasan Udhayabanu, Veedamali S. Subramanian, Trevor Teafatiller et al. · Clinica Chimica Acta · 2016 · 29 citations

Life Sciences, Genetics, Molecular Genetics +10

Adaptive regulation of riboflavin transport in heart: effect of dietary riboflavin deficiency in cardiovascular pathogenesis

Tamilarasan Udhayabanu, Sellamuthu Karthi, Ayyavu Mahesh et al. · Molecular and Cellular Biochemistry · 2017 · 17 citations

Life Sciences, Nutritional Sciences, Physiology +17

Brown−Vialetto−Van Laere and Fazio−Londe syndromes: <i>SLC52A3</i> mutations with puzzling phenotypes and inheritance

Santhalingam Gayathri, Vykuntaraju K. Gowda, Tamilarasan Udhayabanu et al. · European Journal of Neurology · 2020 · 13 citations

Life Sciences, Genetics, Molecular Genetics +16

Fazio-Londe syndrome in siblings from India with different phenotypes

Vykuntaraju K. Gowda, Tamilarasan Udhayabanu, Perumal Varalakshmi et al. · Brain and Development · 2018 · 11 citations

Life Sciences, Genetics, Pediatrics +10