Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2007 | 1 |
2016 | 1 |
2023 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
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.
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 …
Item in Clipboard
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 …
Item in Clipboard
Cite
Cite