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Influence of the Inherited Glucose-6-phosphate Dehydrogenase Deficiency on the Appearance of Neonatal Hyperbilirubinemia in Southern Croatia
BACKGROUND: Neonatal hyperbilirubinemia is a common clinical manifestation of the inherited glucose-6-phosphate dehydrogenase (G6PD) deficiency. AIM OF THE STUDY: The aim of this study was to investigate the influence of the inherited G6PD deficiency on the appearance of neonatal hyperbilirubinemia...
Autores principales: | Cherepnalkovski, Anet Papazovska, Marusic, Eugenija, Piperkova, Katica, Lozic, Bernarda, Skelin, Ana, Gruev, Todor, Krzelj, Vjekoslav |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AVICENA, d.o.o., Sarajevo
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639371/ https://www.ncbi.nlm.nih.gov/pubmed/26635431 http://dx.doi.org/10.5455/aim.2015.23.264-267 |
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