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Journal Abstract Search

152 related items for PubMed ID: 27117574

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  • 2. Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.
    Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH.
    Hemoglobin; 2016; 40(1):64-5. PubMed ID: 26372199
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  • 3. A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin.
    Serjeant GR, Serjeant BE, Hambleton IR, Oakley M, Thein SL, Clark B.
    Hemoglobin; 2017 May; 41(3):216-217. PubMed ID: 28870138
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  • 9. Coinheritance of α-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia.
    Belisário AR, Rodrigues CV, Martins ML, Silva CM, Viana MB.
    Hemoglobin; 2010 May; 34(6):516-29. PubMed ID: 21077759
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  • 11. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
    Prakobkaew N, Fucharoen S, Fuchareon G, Siriratmanawong N.
    Eur J Haematol; 2014 Jan; 92(1):73-9. PubMed ID: 24112054
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  • 12. Massive splenic infarction in an adolescent with hemoglobin S-HPFH.
    Whyte D, Forget B, Chui DH, Luo HY, Pashankar F.
    Pediatr Blood Cancer; 2013 Jul; 60(7):E49-51. PubMed ID: 23281181
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  • 13. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.
    Andersson BA, Wering ME, Luo HY, Basran RK, Steinberg MH, Smith HP, Chui DH.
    Eur J Haematol; 2007 Jan; 78(1):82-5. PubMed ID: 17038017
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  • 15. Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
    Carrocini GC, Ondei LS, Zamaro PJ, Bonini-Domingos CR.
    Genet Mol Res; 2011 Dec 21; 10(4):3213-9. PubMed ID: 22194178
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  • 16. The relative levels of beta A and beta S mRNAs in Hb S heterozygotes and in patients with Hb S-beta(+)-thalassaemia or Hb S-beta(+)-HPFH combinations.
    Dimovski AJ, Efremov DG, Gu LH, Huisman TH.
    Br J Haematol; 1994 Jun 21; 87(2):353-6. PubMed ID: 7524623
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  • 17. Molecular characterization of hereditary persistence of fetal hemoglobin in the Karen people of Thailand.
    Trachoo O, Sura T, Sakuntabhai A, Singhasivanon P, Krudsood S, Phimpraphi W, Krasaesub S, Chanjarunee S, Looareesuwan S.
    Hemoglobin; 2003 May 21; 27(2):97-104. PubMed ID: 12779271
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  • 19. Case Report of Acute Splenic Sequestration Crisis in an Adult Patient with Hb S Disease and Suspected Hereditary Persistence of Fetal Hemoglobin.
    Sigal IR, Ciunci CA.
    Hemoglobin; 2021 Jan 21; 45(1):60-61. PubMed ID: 33588663
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  • 20. Quantitation of three types of gamma chain of HbF by high pressure liquid chromatography; application of this method to the HbF of patients with sickle cell anemia or the S-HPFH condition.
    Huisman TH, Altay C, Webber B, Reese AL, Gravely ME, Okonjo K, Wilson JB.
    Blood; 1981 Jan 21; 57(1):75-82. PubMed ID: 6160889
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