467 related articles for article (PubMed ID: 14688008)
1. Spontaneous mutation of the hemoglobin Leiden (beta 6 or 7 Glu-->0) in a Thai girl.
Sanguansermsri P; Shimbhu D; Wongvilairat R; Pimsorn C; Sanguansermsri T
Haematologica; 2003 Dec; 88(12):ECR35. PubMed ID: 14688008
[TBL] [Abstract][Full Text] [Related]
2. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.
Tan J; Tay JS; Wong YC; Kham SK; Bte Abd Aziz N; Teo SH; Wong HB
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():252-6. PubMed ID: 8629117
[TBL] [Abstract][Full Text] [Related]
3. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients.
Changtrakun Y; Fucharoen S; Ayukarn K; Siriratmanawong N; Fucharoen G; Sanchaisuriya K
Ann Hematol; 2002 Jul; 81(7):389-93. PubMed ID: 12185510
[TBL] [Abstract][Full Text] [Related]
4. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.
Siriratmanawong N; Chansri W; Singsanan S; Fucharoen G; Fucharoen S
Hemoglobin; 2009; 33(6):507-14. PubMed ID: 19958198
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Dominantly Inherited beta-Thalassemia.
Efremov GD
Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
[TBL] [Abstract][Full Text] [Related]
7. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy.
Sanchaisuriya K; Chunpanich S; Fucharoen S; Fucharoen G; Sanchaisuriya P; Changtrakun Y
Eur J Haematol; 2005 Mar; 74(3):221-7. PubMed ID: 15693792
[TBL] [Abstract][Full Text] [Related]
8. Compound heterozygosity of Hb D(Iran) (beta(22) Glu-->Gln) and beta(0)-thalassemia (619 bp-deletion) in India.
Agrawal MG; Bhanushali AA; Dedhia P; Jeswani KD; Dayanand S; Dasgupta A; Das BR
Eur J Haematol; 2007 Sep; 79(3):248-50. PubMed ID: 17655708
[TBL] [Abstract][Full Text] [Related]
9. Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients.
Fucharoen S; Sanchaisuriya K; Fucharoen G; Surapot S
Haematologica; 2001 Jun; 86(6):657-8. PubMed ID: 11418377
[No Abstract] [Full Text] [Related]
10. Thalassemia intermedia associated with complex interaction of Hb Beijing [alpha16(A14)Lys-->Asn] and Hb E [beta26(B8)Glu-->Lys] with a deletional alpha-thalassemia-1 in a Thai family.
Fucharoen S; Chunpanich S; Sanchaisuriya K; Fucharoen G; Kunyanone N
Hemoglobin; 2005; 29(1):77-83. PubMed ID: 15768559
[TBL] [Abstract][Full Text] [Related]
11. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand.
Chunpanich S; Ayukarn K; Sanchaisuriya K; Fucharoen G; Fucharoen S
Clin Lab Haematol; 2004 Oct; 26(5):355-8. PubMed ID: 15485467
[TBL] [Abstract][Full Text] [Related]
12. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
[TBL] [Abstract][Full Text] [Related]
13. Complex interaction of Hb Hekinan [alpha27(B8) Glu-Asp] and Hb E [beta26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family.
Fucharoen S; Changtrakun Y; Ratanasiri T; Fucharoen G; Sanchaisuriya K
Eur J Haematol; 2003 May; 70(5):304-9. PubMed ID: 12694166
[TBL] [Abstract][Full Text] [Related]
14. Severe beta(0) thalassemia/hemoglobin E disease caused by de novo 22-base pair duplication in the paternal allele of beta globin gene.
Rojnuckarin P; Settapiboon R; Vanichsetakul P; Sueblinvong T; Sutcharitchan P
Am J Hematol; 2007 Jul; 82(7):663-5. PubMed ID: 17160997
[TBL] [Abstract][Full Text] [Related]
15. Hematological and molecular characterization of beta-thalassemia/Hb Tak compound heterozygote.
Charoenkwan P; Thanarattanakorn P; Chaovaluksakul S; Sittipreechacharn S; Sae-Tang R; Sanguansermsri T
Southeast Asian J Trop Med Public Health; 2003 Jun; 34(2):415-9. PubMed ID: 12971573
[TBL] [Abstract][Full Text] [Related]
16. Hemoglobin Lepore EF Bart's disease: a molecular, hematological, and diagnostic aspects.
Chaibunruang A; Fucharoen G; Jetsrisuparb A; Fucharoen S
Ann Hematol; 2011 Nov; 90(11):1337-40. PubMed ID: 21302111
[TBL] [Abstract][Full Text] [Related]
17. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine).
Coleman MB; Lu ZH; Smith CM; Adams JG; Harrell A; Plonczynski M; Steinberg MH
J Clin Invest; 1995 Feb; 95(2):503-9. PubMed ID: 7860732
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia.
Chen XW; Mo QH; Li Q; Zeng R; Xu XM
Ann Hematol; 2007 Sep; 86(9):653-7. PubMed ID: 17516066
[TBL] [Abstract][Full Text] [Related]
19. Compound heterozygote states for Hb C/Hb Malay and Hb C/Hb E in pregnancy: a molecular and hematological analysis.
Fucharoen S; Fucharoen G; Sanchaisuriya K; Surapot S
Blood Cells Mol Dis; 2005; 35(2):196-200. PubMed ID: 15982909
[TBL] [Abstract][Full Text] [Related]
20. Compound heterozygous Hb Tak/Hb E causes secondary erythrocytosis in a Thai family.
Teawtrakul N; Sirijirachai C; Chansung G; Fucharoen G
Hemoglobin; 2010 Jan; 34(2):165-8. PubMed ID: 20353353
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]