Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases von Udhayabanu, Tamilarasan, Manole, Andreea, Rajeshwari, Mohan, Varalakshmi, Perumal, Houlden, Henry, Ashokkumar, Balasubramaniem

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Fazio-Londe syndrome in siblings from India with different phenotypes von Gowda, Vykuntaraju K., Udhayabanu, Tamilarasan, Varalakshmi, Perumal, Srinivasan, Varunvenkat M., Ashokkumar, Balasubramaniem

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Brown−Vialetto−Van Laere and Fazio−Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance von Gayathri, Santhalingam, Gowda, Vykuntaraju K., Udhayabanu, Tamilarasan, O'Callaghan, Benjamin, Efthymiou, Stephanie, Varalakshmi, Perumal, Benakappa, Naveen, Houlden, Henry, Ashokkumar, Balasubramaniem

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Adaptive regulation of riboflavin transport in heart: effect of dietary riboflavin deficiency in cardiovascular pathogenesis von Udhayabanu, Tamilarasan, Karthi, Sellamuthu, Mahesh, Ayyavu, Varalakshmi, Perumal, Manole, Andreea, Houlden, Henry, Ashokkumar, Balasubramaniem

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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 von Udhayabanu, Tamilarasan, Subramanian, Veedamali S, Teafatiller, Trevor, Gowda, Vykuntaraju K, Raghavan, Varun S, Varalakshmi, Perumal, Said, Hamid M, Ashokkumar, Balasubramaniem

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