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Quoted phrase not found in phrase index: "Sickle cell-hemoglobin E disease syndrome"
Page 1
Most adults with severe HbSC disease are not treated with hydroxyurea.
Ghunney WK, Asare EV, Ayete-Nyampong JB, Oppong SA, Rodeghier M, DeBaun MR, Olayemi E. Ghunney WK, et al. Blood Adv. 2023 Jul 11;7(13):3312-3319. doi: 10.1182/bloodadvances.2022009049. Blood Adv. 2023. PMID: 36799926 Free PMC article.
Sickle cell hemoglobin SC (HbSC) disease is the second most frequent sickle cell disease (SCD) genotype after sickle cell anemia (HbSS). ...We identified a comparison group of 639 individuals with HbSS and matched the frequency bas
Sickle cell hemoglobin SC (HbSC) disease is the second most frequent sickle cell disease (SCD) gen
Sickle cell-haemoglobin E (HbSE) compound heterozygosity: a clinical and haematological study.
Knox-Macaulay HH, Ahmed MM, Gravell D, Al-Kindi S, Ganesh A. Knox-Macaulay HH, et al. Int J Lab Hematol. 2007 Aug;29(4):292-301. doi: 10.1111/j.1365-2257.2006.00886.x. Int J Lab Hematol. 2007. PMID: 17617080 Review.
The paucity of clinical reports in the world literature suggests that, as a disease entity, haemoglobin SE compound heterozygosity is of negligible importance. ...At least 50% of those studied were asymptomatic throughout the study period but sickling-related compli …
The paucity of clinical reports in the world literature suggests that, as a disease entity, haemoglobin SE compound heterozygosity is …
Rheology of red blood cells in patients with HbC disease.
Lemonne N, Billaud M, Waltz X, Romana M, Hierso R, Etienne-Julan M, Connes P. Lemonne N, et al. Clin Hemorheol Microcirc. 2016;61(4):571-7. doi: 10.3233/CH-141906. Clin Hemorheol Microcirc. 2016. PMID: 25335812
Patients with hemoglobin C disease (CC) usually do not develop severe complications in comparison with individuals with sickle cell anemia (SS) or with sickle cell hemoglobin C disease (SC). ...Blood viscosity was measured at 225 s(-1) wi …
Patients with hemoglobin C disease (CC) usually do not develop severe complications in comparison with individuals with sickle