Sickle Cell Disease - Pain and Common Chronic Complications 2016
DOI: 10.5772/65648
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Introductory Chapter: Introduction to the History, Pathology and Clinical Management of Sickle Cell Disease

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Cited by 6 publications
(2 citation statements)
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References 62 publications
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“…In the United States, 1 in 600 African-Americans has been diagnosed with SCD [1,2], and it was reported that 1 in every 2000 births had SCD during a newborn screening programme in the United Kingdom [11,18]. This multisystem disorder results in the sickling of red blood cells, which can cause a range of complications such as micro-vascular occlusion, haemolysis and progressive organ failure [4,14,8].…”
Section: Introductionmentioning
confidence: 99%
“…In the United States, 1 in 600 African-Americans has been diagnosed with SCD [1,2], and it was reported that 1 in every 2000 births had SCD during a newborn screening programme in the United Kingdom [11,18]. This multisystem disorder results in the sickling of red blood cells, which can cause a range of complications such as micro-vascular occlusion, haemolysis and progressive organ failure [4,14,8].…”
Section: Introductionmentioning
confidence: 99%
“…Όταν οι παραπάνω συνθήκες δεν εκπληρούνται, υπάρχει πλήρης ή μερική έλλειψη του ενός ή και των δύο αλλήλων της σφαιρίνης (Viprakasit & Origa, 2014). [Weatherall, 2011: Modell, Darlison, Birgens, Cario, Faustino, Giordano, et al, 2007 (Inusa, Casale, & Ward, 2016). Εκατό χρόνια μετά την αρχική έκθεση του Herrick, σημειώθηκαν σημαντικές προόδους στη διάγνωση και τη διαχείριση (Inati, 2009).…”
Section: δομή σύνθεση και λειτουργία αιμοσφαιρινώνunclassified