Bladder injury in an incarcerated inguinal hernia in a pediatric patient

بواسطة Gunadi, Gunadi, Oktavian, Arif, Iskandar, Kristy, Vujira, Khanza Adzkia, Fauzi, Aditya Rifqi
منشور في 2022

The impact of NRG1 expressions and methylation on multifactorial Hirschsprung disease

بواسطة Gunadi, Gunadi, Kalim, Alvin Santoso, Marcellus, Marcellus, Budi, Nova Yuli Prasetyo, Iskandar, Kristy
منشور في 2022

The impact of NRG1 expressions and methylation on multifactorial Hirschsprung disease

بواسطة Gunadi, Gunadi, Kalim, Alvin Santoso, Marcellus, Marcellus, Budi, Nova Yuli Prasetyo, Iskandar, Kristy
منشور في 2022

Association between prognostic factors and the clinical deterioration of preterm neonates with necrotizing enterocolitis

بواسطة Ibrohim, Ibnu Sina, Pratama, Henggar Allest, Fauzi, Aditya Rifqi, Iskandar, Kristy, Agustriani, Nunik, Gunadi, Gunadi
منشور في 2022

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

بواسطة Triono, Agung, Iskandar, Kristy, Nugrahanto, Andika Priamas, Hadiyanto, Marissa Leviani, Gunadi, Gunadi, Herini, Elisabeth Siti
منشور في 2022

Long-term functional outcomes of patients with Hirschsprung disease following pull-through

بواسطة Gunadi, Gunadi, Carissa, Theodora Monica, Stevie, Stevie, Daulay, Ezzah Fatmala, Yulianda, Dicky, Iskandar, Kristy, Dwihantoro, Andi
منشور في 2022

Phylogenetic analysis of congenital rubella virus from Indonesia: a case report

بواسطة Herini, Elisabeth Siti, Triono, Agung, Iskandar, Kristy, Nuady, Albaaza, Pujiastuti, Lucia Hetty, Marcellus, Marcellus, Nugrahanto, Andika Priamas, Kamal, Musthofa, Gunadi, Gunadi
منشور في 2022

Phylogenetic Analysis of Congenital Rubella Virus from Indonesia: a case report

بواسطة Herini, Elisabeth Siti, Triono, Agung, Iskandar, Kristy, Nuady, Albaaza, Pujiastuti, Lucia Hetty, Marcellus, Marcellus, Nugrahanto, Andika Priamas, Kamal, Musthofa, Gunadi, Gunadi
منشور في 2022

Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report

بواسطة Iskandar, Kristy, Sunartini, Sunartini, Astari, Farida Niken, Gumilang, Rizki Amalia, Ilma, Nissya, Shartyanie, Ni Putu, Adistyawan, Guritno, Tan, Grace, Gunadi, Gunadi, Lai, Poh San
منشور في 2022

Effect of semaphorin 3C gene variants in multifactorial Hirschsprung disease

بواسطة Gunadi, Ryantono, Fiko, Sethi, Raman, Marcellus, Kalim, Alvin Santoso, Imelda, Priscillia, Melati, Devy, Simanjaya, Susan, Widitjiarso, William, Pitaka, Ririd Tri, Arfian, Nur, Iskandar, Kristy, Makhmudi, Akhmad, Lai, Poh San
منشور في 2021