131 related articles for article (PubMed ID: 7524623)
1. 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; 87(2):353-6. PubMed ID: 7524623
[TBL] [Abstract][Full Text] [Related]
2. gamma-mRNA and Hb F levels in beta-thalassaemia.
Efremov DG; Dimovski AJ; Sukarova E; Schilirò G; Zisovski N; Efremov GD; Burrone OR; Huisman TH
Br J Haematol; 1994 Oct; 88(2):311-7. PubMed ID: 7528532
[TBL] [Abstract][Full Text] [Related]
3. Globin mRNA in beta-thalassemia heterozygotes with different beta-thalassemia alleles and in heterozygotes for hereditary persistence of fetal hemoglobin.
Smetanina NS; Adekile AD; Huisman TH
Acta Haematol; 1996; 96(3):162-9. PubMed ID: 8876614
[TBL] [Abstract][Full Text] [Related]
4. Variations in globin chain synthesis in hereditary persistence of fetal haemoglobin.
Friedman S; Schwartz E; Ahern E; Ahern V
Br J Haematol; 1976 Mar; 32(3):357-64. PubMed ID: 1252370
[TBL] [Abstract][Full Text] [Related]
5. The -158 (C-->T) promoter mutation is responsible for the increased transcription of the 3' gamma gene in the Atlanta type of hereditary persistence of fetal hemoglobin.
Efremov DG; Dimovski AJ; Huisman TH
Blood; 1994 Jun; 83(11):3350-5. PubMed ID: 7514907
[TBL] [Abstract][Full Text] [Related]
6. Occurrence of G gamma Hb F in Greek HPFH: analysis of heterozygotes and compound heterozygotes with beta thalassaemia.
Clegg JB; Metaxatou-Mavromati A; Kattamis C; Sofroniadou K; Wood WG; Weatherall DJ
Br J Haematol; 1979 Dec; 43(4):521-36. PubMed ID: 93488
[TBL] [Abstract][Full Text] [Related]
7. Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.
Indrak K; Indrakova J; Kutlar F; Pospisilova D; Sulovska I; Baysal E; Huisman TH
Ann Hematol; 1991 Aug; 63(2):111-5. PubMed ID: 1716997
[TBL] [Abstract][Full Text] [Related]
8. Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant.
Losekoot M; Fodde R; Gerritsen EJ; van de Kuit I; Schreuder A; Giordano PC; Vossen JM; Bernini LF
Blood; 1991 Feb; 77(4):861-7. PubMed ID: 1704267
[TBL] [Abstract][Full Text] [Related]
9. 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; 27(2):97-104. PubMed ID: 12779271
[TBL] [Abstract][Full Text] [Related]
10. Fetal hemoglobin expression in compound heterozygotes for -117 (G-->A)A gamma HPFH and beta zero 39 nonsense thalassemia.
Pistidda P; Frogheri L; Oggiano L; Guiso L; Manca L; Dore F; Masala B; Gilman JG; Longinotti M
Am J Hematol; 1995 Aug; 49(4):267-70. PubMed ID: 7543730
[TBL] [Abstract][Full Text] [Related]
11. Molecular characterization and PCR detection of a deletional HPFH: application to rapid prenatal diagnosis for compound heterozygotes of this defect with beta-thalassemia in a Chinese family.
Xu XM; Li ZQ; Liu ZY; Zhong XL; Zhao YZ; Mo QH
Am J Hematol; 2000 Nov; 65(3):183-8. PubMed ID: 11074532
[TBL] [Abstract][Full Text] [Related]
12. The gamma chain heterogeneity of fetal hemoglobin in black beta-thalassemia and HPFH heterozygotes.
Huisman TH; Gravely ME; Webber B; Okonjo K; Henson J; Reese AL
Blood; 1981 Jul; 58(1):62-70. PubMed ID: 6165415
[TBL] [Abstract][Full Text] [Related]
13. Heterocellular hereditary persistence of fetal haemoglobin affects the haematological parameters of beta-thalassaemia trait.
Garner C; Dew TK; Sherwood R; Rees D; Thein SL
Br J Haematol; 2003 Oct; 123(2):353-8. PubMed ID: 14531920
[TBL] [Abstract][Full Text] [Related]
14. The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adults and newborn.
Huisman TH; Efremov GD; Reese AL; Howard JS; Gravely ME; Harris HF; Wilson JB
Hemoglobin; 1979; 3(4):223-52. PubMed ID: 500369
[TBL] [Abstract][Full Text] [Related]
15. Adult and fetal hemoglobin production in erythroid colonies from subjects with beta-thalassemia or with hereditary persistance of fetal hemoglobin (HPFH).
Huisman TH; Reese AL; Gravely ME; Wilson JB; Webber B; Felice AE
Hemoglobin; 1980; 4(3-4):449-67. PubMed ID: 6158501
[TBL] [Abstract][Full Text] [Related]
16. Wide range of F cell levels in healthy Thai adults: Influence of Swiss-type hereditary persistence of foetal haemoglobin & β-haemoglobinopathy.
Tatu T
Indian J Med Res; 2019 Aug; 150(2):161-166. PubMed ID: 31670271
[TBL] [Abstract][Full Text] [Related]
17. The Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, Brazil.
Belisário AR; Sales RR; Silva CM; Velloso-Rodrigues C; Viana MB
Hemoglobin; 2016 Jun; 40(3):215-9. PubMed ID: 27117574
[TBL] [Abstract][Full Text] [Related]
18. 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
[TBL] [Abstract][Full Text] [Related]
19. Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India.
Patel DK; Patel M; Mashon RS; Patel S; Dash PM; Das BS
Hemoglobin; 2010; 34(6):604-9. PubMed ID: 21077771
[TBL] [Abstract][Full Text] [Related]
20. Molecular characterization of thalassemia intermedia associated with HPFH-6/beta-thalassemia and HPFH-6/Hb E in Thai patients.
Fucharoen S; Fucharoen G; Sanchaisuriya K; Surapot S
Acta Haematol; 2002; 108(3):157-61. PubMed ID: 12373089
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
