GLRX5-associated [Fe-S] cluster biogenesis disorder: further characterisation of the neurological phenotype and long-term outcome

por Sankaran, Bindu Parayil, Gupta, Sachin, Tchan, Michel, Devanapalli, Beena, Rahman, Yusof, Procopis, Peter, Bhattacharya, Kaustuv
Publicado 2021

Challenges in Diagnosing Intermediate Maple Syrup Urine Disease by Newborn Screening and Functional Validation of Genomic Results Imperative for Reproductive Family Planning

por Sajeev, Mona, Chin, Sharon, Ho, Gladys, Bennetts, Bruce, Sankaran, Bindu Parayil, Gutierrez, Bea, Devanapalli, Beena, Tolun, Adviye Ayper, Wiley, Veronica, Fletcher, Janice, Fuller, Maria, Balasubramaniam, Shanti
Publicado 2021

Functional network connectivity imprint in febrile seizures

por Acharya, Ullas V., Kulanthaivelu, Karthik, Panda, Rajanikant, Saini, Jitender, Gupta, Arun K., Sankaran, Bindu Parayil, Raghavendra, Kenchaiah, Mundlamuri, Ravindranath Chowdary, Sinha, Sanjib, Keshavamurthy, M. L., Bharath, Rose Dawn
Publicado 2022

Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome

por Chakrabarty, Sanjiban, Govindaraj, Periyasamy, Sankaran, Bindu Parayil, Nagappa, Madhu, Kabekkodu, Shama Prasada, Jayaram, Pradyumna, Mallya, Sandeep, Deepha, Sekar, Ponmalar, J. N. Jessiena, Arivinda, Hanumanthapura R., Meena, Angamuthu Kanikannan, Jha, Rajan Kumar, Sinha, Sanjib, Gayathri, Narayanappa, Taly, Arun B., Thangaraj, Kumarasamy, Satyamoorthy, Kapaettu
Publicado 2021