TY  - BOOK
AU  - Colombatti, Raffaella||Cela, Elena||Lobitz, Stephan||Elion, Jacques
TI  - Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies
KW  - glucose-6-phosphate dehydrogenase||hydroxyurea/hydroxycarbamide||n/a||cord blood||screening||hemoglobin pattern||capillary electrophoresis||sickle cell disease||(recommended) screening panel||vaso-occlusive crisis||Guthrie spots||newborn screening)||foetal haemoglobin||harmonisation||review||birth prevalence||G6PD deficiency||prevention||end-organ damage||thalassemia||MALDI-TOF||IEF||acute chest syndrome||India||sickle cell and thalassaemia screening programme||‘Getting to Outcomes’||newborn screening||hemoglobinopathy||service users||public health engagement||automated HPLC||Kaduna State||gene therapy for haemoglobinopathies||?-globin gene||methods||neonatal screening program||malaria||Plasmodium vivax||sub-Saharan Africa||patient organisations||health policy||pathophysiology||Sickle Cell Disease||mass spectrometry||sickle cell disorder||neonatal screening||non-tribal||Nigeria||point-of-care||HPLC||laboratory methods||registry||patient advocacy||bone marrow transplant||anaemia||hemoglobinopathies||tribal||newborn||burden of disease||patient representatives||diagnostics||policy making||haemolysis||Caribbean||high performance liquid chromatography (HPLC)||sickle cell disease (SCD)||implementation science
UR  - https://mdpi.com/books/pdfview/book/1649
ER  -