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Tamilarasan Udhayabanu

Showing results (1-10 of 5) with videos related to

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Brain & Development|March 5, 2018
Fazio-Londe syndrome in siblings from India with different phenotypesVykuntaraju K Gowda, Tamilarasan Udhayabanu, Perumal Varalakshmi, et al.
Journal of Clinical Medicine|May 6, 2017
Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative DiseasesTamilarasan Udhayabanu, Andreea Manole, Mohan Rajeshwari, et al.
Molecular and Cellular Biochemistry|August 25, 2017
Adaptive regulation of riboflavin transport in heart: effect of dietary riboflavin deficiency in cardiovascular pathogenesisTamilarasan Udhayabanu, Sellamuthu Karthi, Ayyavu Mahesh, et al.
European Journal of Neurology|December 16, 2020
Brown-Vialetto-Van Laere and Fazio-Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritanceSanthalingam Gayathri, Vykuntaraju K Gowda, Tamilarasan Udhayabanu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 6, 2016
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 transportersTamilarasan Udhayabanu, Veedamali S Subramanian, Trevor Teafatiller, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Brain & Development|March 5, 2018
Fazio-Londe syndrome in siblings from India with different phenotypesVykuntaraju K Gowda, Tamilarasan Udhayabanu, Perumal Varalakshmi, et al.
Journal of Clinical Medicine|May 6, 2017
Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative DiseasesTamilarasan Udhayabanu, Andreea Manole, Mohan Rajeshwari, et al.
Molecular and Cellular Biochemistry|August 25, 2017
Adaptive regulation of riboflavin transport in heart: effect of dietary riboflavin deficiency in cardiovascular pathogenesisTamilarasan Udhayabanu, Sellamuthu Karthi, Ayyavu Mahesh, et al.
European Journal of Neurology|December 16, 2020
Brown-Vialetto-Van Laere and Fazio-Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritanceSanthalingam Gayathri, Vykuntaraju K Gowda, Tamilarasan Udhayabanu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 6, 2016
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 transportersTamilarasan Udhayabanu, Veedamali S Subramanian, Trevor Teafatiller, et al.
Pageof 1