Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Abdurahman Sukadi"'
Autor:
Risma Karina Kaban, Asril Aminullah, Rinawati Rohsiswatmo, Badriul Hegar, Abdurahman Sukadi, Peter Graham Davis
Publikováno v:
Paediatrica Indonesiana, Vol 62, Iss 2, Pp 104-14 (2022)
Background Preterm infants are susceptible to the damaging effects of hyperoxia which may lead to bronchopulmonary dysplasia (BPD) and intestinal damage. Hyperoxia also affects intestinal microbiota. The optimal initial FiO2 for the resuscitation of
Externí odkaz:
https://doaj.org/article/1bffb0e4869e491f88e4cad67bf89122
Publikováno v:
Majalah Kedokteran Bandung, Vol 43, Iss 4, Pp 193-198 (2011)
Steroid resistant nephrotic syndrome (SRNS) due to nephrotic syndrome type 2 (NPHS2) gene mutation has more severe clinical manifestation than those without mutation. This study was designed to find NPHS2 gene mutation in 412C→T and 419delG in Indo
Externí odkaz:
https://doaj.org/article/640c26845313487788561d835441209a
Publikováno v:
Paediatrica Indonesiana, Vol 51, Iss 5, Pp 272-6 (2011)
Background Steroid-resistant nephrotic syndrome (SRNS) often develops into end stage renal disease. Previous studies have reported that NPHS2 gene mutation, gender, and atopic history are risk factors associated with SRNS. Interethnic, sociocultural,
Externí odkaz:
https://doaj.org/article/5c378c14f9644384a326f6d4aef3260a
Autor:
Peter Graham Davis, Abdurahman Sukadi, Badriul Hegar, Rinawati Rohsiswatmo, Asril Aminullah, Risma Karina Kaban
Publikováno v:
Paediatrica Indonesiana. 62:104-14
Background Preterm infants are susceptible to the damaging effects of hyperoxia which may lead to bronchopulmonary dysplasia (BPD) and intestinal damage. Hyperoxia also affects intestinal microbiota. The optimal initial FiO2 for the resuscitation of
Publikováno v:
Majalah Kedokteran Bandung, Vol 43, Iss 4, Pp 193-198 (2011)
Steroid resistant nephrotic syndrome (SRNS) due to nephrotic syndrome type 2 (NPHS2) gene mutation has more severe clinical manifestation than those without mutation. This study was designed to find NPHS2 gene mutation in 412C→T and 419delG in Indo
Autor:
Abdurahman Sukadi, Anna Alisjahbana
Publikováno v:
Paediatrica Indonesiana. 14:63
The purpose of this paper is toreport a case of neonatal polycythe-mia thought to be caused by delayedcord clamping. Maternal-fetal trans-fusion is also a probable cause.