256 related articles for article (PubMed ID: 31670271)
1. 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]
2. Effect of Swiss-type heterocellular HPFH from XmnI-Gγ and HBBP1 polymorphisms on HbF, HbE, MCV and MCH levels in Thai HbE carriers.
Kerdpoo S; Limweeraprajak E; Tatu T
Int J Hematol; 2014 Mar; 99(3):338-44. PubMed ID: 24474642
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.
Fucharoen S; Pengjam Y; Surapot S; Fucharoen G; Sanchaisuriya K
Am J Hematol; 2002 Oct; 71(2):109-13. PubMed ID: 12353310
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
Adeyemo T; Ojewunmi O; Oyetunji A
Pan Afr Med J; 2014; 18():71. PubMed ID: 25400838
[TBL] [Abstract][Full Text] [Related]
7. Genetic Blood Disorders Survey in the Sultanate of Oman.
Al-Riyami A; Ebrahim GJ
J Trop Pediatr; 2003 Jul; 49 Suppl 1():i1-20. PubMed ID: 12934793
[TBL] [Abstract][Full Text] [Related]
8. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
Panyasai S; Fucharoen S; Surapot S; Fucharoen G; Sanchaisuriya K
Haematologica; 2004 Jul; 89(7):777-81. PubMed ID: 15257928
[TBL] [Abstract][Full Text] [Related]
9. [Genetically based states of elevated quantity of foetal haemoglobin (Hb F) in healthy individuals and patients].
Musielak M
Pol Merkur Lekarski; 2011 Jan; 30(175):62-5. PubMed ID: 21542248
[TBL] [Abstract][Full Text] [Related]
10. Automatic measurement of hemoglobin F in blood obtained from patients with hemoglobin E/E and beta-thalassemia/hemoglobin/E.
Tatsumi N; Tsuda I; Funahara Y; Bunyaratvej A; Fucharoen S
Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():91-4. PubMed ID: 1284356
[TBL] [Abstract][Full Text] [Related]
11. Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin.
Ngo DA; Aygun B; Akinsheye I; Hankins JS; Bhan I; Luo HY; Steinberg MH; Chui DH
Br J Haematol; 2012 Jan; 156(2):259-64. PubMed ID: 22017641
[TBL] [Abstract][Full Text] [Related]
12. α-Haemoglobin stabilising protein expression is influenced by mean cell haemoglobin and HbF levels in HbE/β-thalassaemia individuals.
Lim WF; Muniandi L; George E; Sathar J; Teh LK; Gan GG; Lai MI
Blood Cells Mol Dis; 2012 Jan; 48(1):17-21. PubMed ID: 22079025
[TBL] [Abstract][Full Text] [Related]
13. Haemoglobin E/beta-thalassaemia - an experience in the eastern Indian state of Orissa.
Chhotray GP; Dash BP; Ranjit MR; Cohla RB; Mohanty D
Acta Haematol; 2003; 109(4):214-6. PubMed ID: 12853699
[No Abstract] [Full Text] [Related]
14. Nineteen years study of beta-thalassaemia in Slovakia.
Fábryová V; Babusík P; Laluhová-Striezencová Z; Drakulová M; Oslancová M; Macichová M; Sakalová A
Cent Eur J Public Health; 2012 Dec; 20(4):239-43. PubMed ID: 23441384
[TBL] [Abstract][Full Text] [Related]
15. Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait.
Velasco-Rodríguez D; Alonso-Domínguez JM; González-Fernández FA; Muriel A; Abalo L; Sopeña M; Villarrubia J; Ropero P; Plaza MP; Tenorio M; Jiménez-Martín A; Moreno G; Martínez-Nieto J; de la Fuente-Gonzalo F; Fernández-Escribano M; López-Jiménez FJ; Cava F
J Clin Pathol; 2016 Oct; 69(10):912-20. PubMed ID: 26915371
[TBL] [Abstract][Full Text] [Related]
16. Genetic determinants related to pharmacological induction of foetal haemoglobin in transfusion-dependent HbE-β thalassaemia.
Biswas S; Nag A; Ghosh K; Ray R; Roy K; Bandyopadhyay A; Bhattacharyya M
Ann Hematol; 2019 Feb; 98(2):289-299. PubMed ID: 30413899
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Compound heterozygote state for GgammaAgamma(deltabeta) degrees -thalassemia and hereditary persistence of fetal hemoglobin.
Fucharoen S; Panyasai S; Surapot S; Fucharoen G; Sanchaisuriya K
Am J Hematol; 2005 Oct; 80(2):119-23. PubMed ID: 16184575
[TBL] [Abstract][Full Text] [Related]
19. Mutation spectrum and erythrocyte indices characterisation of α-thalassaemia and β-thalassaemia in Sichuan women in China: a thalassaemia screening survey of 42 155 women.
Li B; Han X; Ma J; Yang D
J Clin Pathol; 2021 Mar; 74(3):182-186. PubMed ID: 32719015
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
