Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Nardlada Hhantikul"'
Autor:
Nattasit Pienthai, Chedtapak Ruengdit, Suphara Manowong, Kanyakan Kongthai, Kritsanee Maneewong, Kankanitta Pongmorn, Maneewan Inta, Nardlada Hhantikul, Aungkana Saejeng, Sakorn Pornprasert
Publikováno v:
Journal of Associated Medical Sciences, Vol 52, Iss 1, Pp 79-83 (2018)
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited enzymatic disorder associated with severe neonatal hyperbilirubinemia and acute hemolysis after exposure to certain drugs or infections. The most common test for screenin
Externí odkaz:
https://doaj.org/article/051de04d0fd5489aa067bfe837acaaa3
Autor:
Nattasit Pienthai, Chedtapak Ruengdit, Suphara Manowong, Kanyakan Kongthai, Kritsanee Maneewong, Kankanitta Pongmorn, Maneewan Inta, Nardlada Hhantikul, Aungkana Saejeng, Sakorn PornprasertNattasit Pienthai, Sakorn Pornprasert
Journal of Associated Medical Sciences, 52, 1, 78-82
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c372bd23a5becebfdea05dcdf277817d