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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...

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Detalles Bibliográficos
Autores principales:	Cherepnalkovski, Anet Papazovska, Marusic, Eugenija, Piperkova, Katica, Lozic, Bernarda, Skelin, Ana, Gruev, Todor, Krzelj, Vjekoslav
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	AVICENA, d.o.o., Sarajevo 2015
Materias:	Original Paper
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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