The role of whole exome sequencing in the UBE3A point mutation of Angelman Syndrome: A case report

por Triono, Agung, Iskandar, Kristy, Nugrahanto, Andika Priamas, Hadiyanto, Marissa Leviani, Gunadi, Herini, Elisabeth Siti
Publicado 2021

Identification of the genetic basis of pediatric neurogenetic disorders at a tertiary referral hospital in Indonesia: Contribution of whole exome sequencing

por Triono, Agung, Iskandar, Kristy, Hadiyanto, Marissa Leviani, Nugrahanto, Andika Priamas, Diantika, Kania, Wijayanti, Veronica Wulan, Herini, Elisabeth Siti
Publicado 2023

Neurological Manifestations of COVID-19 Associated Multisystem Inflammatory Syndrome in Children (MIS-C) in Yogyakarta, Indonesia

por Herini, Elisabeth Siti, Iskandar, Kristy, Triono, Agung, Swipratami, Alexandra Widita, Dewi, Yunika Puspa, Hadiyanto, Marissa Leviani, Rosalia, Ignatia, Rizki, Salsabilla Hasna Mutiara
Publicado 2023