201 related articles for article (PubMed ID: 35802781)
21. Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.
Honig GR; Gunay U; Mason RG; Vida LN; Ferenc C
Pediatr Res; 1976 Jun; 10(6):613-20. PubMed ID: 1272638
[TBL] [Abstract][Full Text] [Related]
22. Plasma levels of some coagulation parameters in steady state HBSC disease patients.
Ajuwon MD; Olayemi E; Benneh AA
Pan Afr Med J; 2014; 19():289. PubMed ID: 25870744
[TBL] [Abstract][Full Text] [Related]
23. Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC).
da Guarda CC; Yahouédéhou SCMA; Santiago RP; Neres JSDS; Fernandes CFL; Aleluia MM; Figueiredo CVB; Fiuza LM; Carvalho SP; Oliveira RM; Fonseca CA; Ndidi US; Nascimento VML; Rocha LC; Goncalves MS
PLoS One; 2020; 15(1):e0228399. PubMed ID: 31995624
[TBL] [Abstract][Full Text] [Related]
24. Hydroxyurea (hydroxycarbamide) for sickle cell disease.
Nevitt SJ; Jones AP; Howard J
Cochrane Database Syst Rev; 2017 Apr; 4(4):CD002202. PubMed ID: 28426137
[TBL] [Abstract][Full Text] [Related]
25. Demographics and outcomes of hemoglobin genotype in hospitalized patients with COVID-19 and sickle cell disease in the United States.
Ilerhunmwuwa NP; Inyang L; Wasifuddin M; Aiwuyo H; Tahir M; Hakobyan N; Ankah P; Torere BE; Amaechi UM; Rayapureddy AK; Wang JC
Eur J Haematol; 2023 Oct; 111(4):611-619. PubMed ID: 37477175
[TBL] [Abstract][Full Text] [Related]
26. Unusually High Prevalence of Stroke and Cerebral Vasculopathy in Hemoglobin SC Disease: A Retrospective Single Institution Study.
Sathi BK; Yoshida Y; Weaver MR; Nolan LS; Gruner B; Balasa V; Altes T; Leiva-Salinas C
Acta Haematol; 2022; 145(2):160-169. PubMed ID: 34749363
[TBL] [Abstract][Full Text] [Related]
27. Soluble P-selectin and vascular endothelial growth factor in steady state sickle cell disease: relationship to genotype.
Blann AD; Mohan JS; Bareford D; Lip GY
J Thromb Thrombolysis; 2008 Apr; 25(2):185-9. PubMed ID: 18080800
[TBL] [Abstract][Full Text] [Related]
28. Ocular Manifestations of Sickle Cell Disease in Different Genotypes.
AlRyalat SA; Jaber BAM; Alzarea AA; Alzarea AA; Alosaimi WA; Al Saad M
Ophthalmic Epidemiol; 2021 Jun; 28(3):185-190. PubMed ID: 32757703
[TBL] [Abstract][Full Text] [Related]
29. Higher rates of hemolysis are not associated with albuminuria in Jamaicans with sickle cell disease.
Asnani MR; Fraser RA; Reid ME
PLoS One; 2011 Apr; 6(4):e18863. PubMed ID: 21533141
[TBL] [Abstract][Full Text] [Related]
30. Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease.
Marcus SJ; Kinney TR; Schultz WH; O'Branski EE; Ware RE
Am J Hematol; 1997 Jan; 54(1):40-6. PubMed ID: 8980259
[TBL] [Abstract][Full Text] [Related]
31. Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of HbSD-Punjab.
Patel DK; Purohit P; Dehury S; Das P; Dutta A; Meher S; Patel S; Bag S; Mashon RS; Das K
Int J Lab Hematol; 2014 Aug; 36(4):444-50. PubMed ID: 24245819
[TBL] [Abstract][Full Text] [Related]
32. Large and medium-sized pulmonary artery obstruction does not play a role of primary importance in the etiology of sickle-cell disease-associated pulmonary hypertension.
van Beers EJ; van Eck-Smit BL; Mac Gillavry MR; van Tuijn CF; van Esser JW; Brandjes DP; Kappers-Klunne MC; Duits AJ; Biemond BJ; Schnog JJ;
Chest; 2008 Mar; 133(3):646-52. PubMed ID: 18198257
[TBL] [Abstract][Full Text] [Related]
33. Profile of Reproductive Issues Associated with Different Sickle Cell Disease Genotypes.
Carvalho FA; Souza AI; Ferreira ALCG; Neto SDS; Oliveira ACPL; Gomes MLRP; Costa MFH
Rev Bras Ginecol Obstet; 2017 Aug; 39(8):397-402. PubMed ID: 28683515
[No Abstract] [Full Text] [Related]
34. Radiographic changes of the jaws in HbSS and HbSC genotypes of sickle cell disease.
Neves FS; de Almeida DA; Oliveira-Santos C; dos Santos JN; Toralles MB; da Silva MC; Campos MI; Crusoé-Rebello I
Spec Care Dentist; 2011; 31(4):129-33. PubMed ID: 21729121
[TBL] [Abstract][Full Text] [Related]
35. [Hemoglobin sickle cell disease: experience of the Yalgado Ouedraogo University Hospital of Ouagadougou, Burkina Faso].
Ayéroué J; Kafando E; Kam L; Gué E; Vertongen F; Ferster A; Cotton F; Gulbis B
Arch Pediatr; 2009 Apr; 16(4):316-21. PubMed ID: 19261452
[TBL] [Abstract][Full Text] [Related]
36. Knowledge insufficient: the management of haemoglobin SC disease.
Pecker LH; Schaefer BA; Luchtman-Jones L
Br J Haematol; 2017 Feb; 176(4):515-526. PubMed ID: 27982424
[TBL] [Abstract][Full Text] [Related]
37. Iron overload in adults with sickle cell disease who have received intermittent red blood cell transfusions.
Pack-Mabien A; Brown B; Herbert DE; Haynes J
J Am Assoc Nurse Pract; 2015 Oct; 27(10):591-6. PubMed ID: 25711464
[TBL] [Abstract][Full Text] [Related]
38. The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.
Rumaney MB; Ngo Bitoungui VJ; Vorster AA; Ramesar R; Kengne AP; Ngogang J; Wonkam A
PLoS One; 2014; 9(6):e100516. PubMed ID: 24978191
[TBL] [Abstract][Full Text] [Related]
39. Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia.
Steinberg MH; Rosenstock W; Coleman MB; Adams JG; Platica O; Cedeno M; Rieder RF; Wilson JT; Milner P; West S
Blood; 1984 Jun; 63(6):1353-60. PubMed ID: 6722353
[TBL] [Abstract][Full Text] [Related]
40. Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassemia, and fetal hemoglobin in HbSS.
Serjeant GR
Expert Rev Hematol; 2022 Feb; 15(2):107-116. PubMed ID: 35143361
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]