Publications and scholarly work
Andrade DM, Jetté N, Chandran I, Patel P, Rubboli G, Cross JH, Craiu D, Tan CT, Kija E, Fung E, Granata T, Hosny H, Mula M, Riney K, Shellhaas RA, Siddiqui M, Zulfiqar Ali Q, Hébert J, Marques P, Kerrigan B, Ji C, Valente K, Carrizosa J, Nabbout R.
A global perspective on transitioning from pediatric to adult care in epilepsy
Epilepsia, 2026
Selvarajah A, Sabo A, Gorodetsky C, Marques PT, Chandran I, Thompson M, Zulfiqar Ali Q, McAndrews MP, Tartaglia MC, Lira VST, Huh L, Connolly M, Rezazadeh A, Qaiser F, Fantaneanu TA, Duong M, Barboza K, Lomax LB, Inuzuka Nakaharada L, Valente K, Arbinuch J, Espindola M, Garzon E, Sorrento G, Meskis MA, Villas N, Hood V, Gonzalez M, Cardenal-Muñoz E, Aiba JA, McKenna L, Linehan C, Hohn S, Auvin S, Devinsky O, Yuen R, Berg AT, Taati B, Fasano A, Andrade DM.
Dravet syndrome: From neurodevelopmental to neurodegenerative disease?
Epilepsia, 2025
Marques PT, Kaka N, Zulfiqar Ali Q, Rong M, Bui E, Andrade DM.
Women With Genetic Epilepsies
Neurol Genet, 2025
Andrade DM, Lira VST, Qaiser F, Zulfiqar Ali Q, Valente K, Lomax LB.
Genetic Epilepsies: Clinical pearls for early career epileptologists
Epilepsy Behav, 2025
Andrade DM, Bassett AS, ZulfiqarAli Q, Lira VST, Reyes NG, Tartaglia MC, Fasano A, Kovacs GG.
Novel neuropathological observations in an adult with Dravet syndrome
Epilepsia, 2025
Andrade DM, Berg AT, Selvarajah A, Sabo A, Gorodetsky C, Marques P, Chandran I, Thompson M, Ali QZ, McAndrews MP, Tartaglia MC, Lira VST, Huh L, Connolly M, Rezazadeh A, Qaiser F, Fantaneanu TA, Duong M, Barboza K, Lomax LB, Nakaharada LI, Arbinuch J, Espindola M, Garzon E, Sorrento G, Meskis MA, Villas N, Hood V, Gonzalez M, Cardenal-Muñoz E, Aibar JA, McKenna L, Linehan C, Yuen R, Taati B, Fasano A, Devinsky O, Valente K.
Evidence demands action: An invitation to share the burden of proof
Epilepsia, 2025
Rong M, Marques PT, Ali QZ, Morcos R, Chandran I, Qaiser F, Møller RS, Bayat A, Rubboli G, Gardella E, Reuter MS, Sands TT, Scheffer IE, Schneider A, Poduri A, Wirrell E, Nabbout R, Sullivan J, Valente K, Auvin S, Knupp KG, Brunklaus A, Aledo-Serrano Á, Andrade DM.
Variants in ATP6V0C are associated with Dravet-like developmental and epileptic encephalopathy
Epilepsia, 2025