Results 131 to 140 of about 34,389 (155)
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2019
Sickle hemoglobin (HbS), so called because of the sickle shape it imparts to deoxynated red cells, is responsible for a wide spectrum of disorders that vary with respect to degree of anemia, frequency of crises, extent of organ injury, and duration of survival. The sickle mutation substitutes thymine for adenine in the sixth codon of the beta-gene (GAG
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Sickle hemoglobin (HbS), so called because of the sickle shape it imparts to deoxynated red cells, is responsible for a wide spectrum of disorders that vary with respect to degree of anemia, frequency of crises, extent of organ injury, and duration of survival. The sickle mutation substitutes thymine for adenine in the sixth codon of the beta-gene (GAG
openaire +1 more source
Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease
New England Journal of Medicine, 2017Kenneth I Ataga +2 more
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A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease
New England Journal of Medicine, 2019Elliott P Vichinsky +2 more
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Fetal haemoglobin in sickle-cell disease: from genetic epidemiology to new therapeutic strategies
Lancet, The, 2016Guillaume Lettre, Daniel E Bauer
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Pathophysiology of Sickle Cell Disease
Annual Review of Pathology: Mechanisms of Disease, 2019Prithu Sundd +2 more
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