Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Nagwan Ibrahim Rashwan"'
Publikováno v:
SVU - International Journal of Medical Sciences, Vol 7, Iss 2, Pp 9-17 (2024)
Background: IRIDA is an inherited recessive anaemia caused by a defect in the TMPRSS6 gene, which codes for the enzyme matriptase-2. This transmembrane serine protease suppresses hepcidin production, an iron regulator (suppressing intestinal absorpti
Externí odkaz:
https://doaj.org/article/a5246dfcc2c642669a611e2ef6f56aa6
Autor:
Eman Ahmed Abd-Elmawgood, Ahmed El-Abd Ahmed, Abdelqader Mohamed Kamel, Nagwan Ibrahim Rashwan
Publikováno v:
SVU - International Journal of Medical Sciences, Vol 3, Iss 2, Pp 61-68 (2020)
Background: Neonatal hyperbilirubinemia is a common problem in neonates with an incidence of about 60% in term babies and 80% in preterm babies. It is the commonest cause of admission to the hospitals in the newborn period. We should assess all babie
Externí odkaz:
https://doaj.org/article/87b9da11f59e40c2880993005fd38319