749 related articles for article (PubMed ID: 18932070)
1. Hb Constant Spring [alpha 142, Term-->Gln (TAA>CAA in alpha2)] in the alpha-thalassemia of anemic patients in Myanmar.
Ne-Win ; Harano K; Harano T; Kyaw-Shwe ; Aye-Aye-Myint ; Khin-Thander-Aye ; Okada S
Hemoglobin; 2008; 32(5):454-61. PubMed ID: 18932070
[TBL] [Abstract][Full Text] [Related]
2. Clinical phenotypes and molecular characterization of Hb H-Paksé disease.
Viprakasit V; Tanphaichitr VS; Pung-Amritt P; Petrarat S; Suwantol L; Fisher C; Higgs DR
Haematologica; 2002 Feb; 87(2):117-25. PubMed ID: 11836160
[TBL] [Abstract][Full Text] [Related]
3. Misdiagnosis of Hb constant spring (alpha142, Term-->Gln, TAA-->CAA in alpha2) in a Hb H (beta4) disease child.
Li D; Liao C; Li J
Hemoglobin; 2007; 31(1):105-8. PubMed ID: 17365012
[TBL] [Abstract][Full Text] [Related]
4. Molecular and clinical features of Hb H disease in northern Thailand.
Charoenkwan P; Taweephon R; Sae-Tung R; Thanarattanakorn P; Sanguansermsri T
Hemoglobin; 2005; 29(2):133-40. PubMed ID: 15921165
[TBL] [Abstract][Full Text] [Related]
5. Simultaneous detection of Hb constant spring (α142, TAA>CAA, α2) and the α2 IVS-I donor site (-TGAGG) deletion by a simple polymerase chain reaction-based method in Iran.
Akhavan-Niaki H; Banihashemi A; Mostafazadeh A; Kholghi Oskooei V; Azizi M; Youssefi Kamangar R; Elmi MM
Hemoglobin; 2012; 36(2):124-30. PubMed ID: 22356652
[TBL] [Abstract][Full Text] [Related]
6. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
Karnpean R; Fucharoen G; Fucharoen S; Sae-ung N; Sanchaisuriya K; Ratanasiri T
Acta Haematol; 2009; 121(4):227-33. PubMed ID: 19546525
[TBL] [Abstract][Full Text] [Related]
7. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
[TBL] [Abstract][Full Text] [Related]
8. [Alpha 2 codon 30 deletion (deltaGAG) causing non-deletional hemoglobin H disease in Guangxi province].
Chen P; Li SQ; Wu H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):435-9. PubMed ID: 15476164
[TBL] [Abstract][Full Text] [Related]
9. Detection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in heterozygotes combined with β-thalassemia.
Li YQ; Li R; Li DZ
Hemoglobin; 2013; 37(2):197-200. PubMed ID: 23390935
[TBL] [Abstract][Full Text] [Related]
10. Hb Koya Dora [alpha142, Term-->Ser (TAA>TCA in alpha2)]: a rare mutation of the alpha2 gene stop codon associated with alpha-thalassemia.
Brennan SO; Ryken S; Chan T
Hemoglobin; 2010; 34(4):402-5. PubMed ID: 20642339
[TBL] [Abstract][Full Text] [Related]
11. Unmasking Hb Paksé (codon 142, TAA>TAT, α2) and its combinations in patients also carrying Hb Constant Spring (codon 142, TAA>CAA, α2) in northern Thailand.
Pornprasert S; Panyasai S; Treesuwan K
Hemoglobin; 2012; 36(5):491-6. PubMed ID: 22881835
[TBL] [Abstract][Full Text] [Related]
12. Screening for Hb Constant Spring in the Guangdong Province, South China, using the Sebia capillary electrophoresis system.
Liao C; Zhou JY; Xie XM; Li DZ
Hemoglobin; 2011; 35(1):87-90. PubMed ID: 21250886
[TBL] [Abstract][Full Text] [Related]
13. The molecular basis of alpha-thalassemia in Thailand.
Winichagoon P; Fucharoen S; Wasi P
Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():7-13. PubMed ID: 1298997
[TBL] [Abstract][Full Text] [Related]
14. Cord blood screening for alpha-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters.
Charoenkwan P; Taweephol R; Sirichotiyakul S; Tantiprabha W; Sae-Tung R; Suanta S; Sakdasirisathaporn P; Sanguansermsri T
Blood Cells Mol Dis; 2010 Jun; 45(1):53-7. PubMed ID: 20299254
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Molecular and hematologic features of hemoglobin E heterozygotes with different forms of alpha-thalassemia in Thailand.
Sanchaisuriya K; Fucharoen G; Sae-ung N; Jetsrisuparb A; Fucharoen S
Ann Hematol; 2003 Oct; 82(10):612-6. PubMed ID: 12955472
[TBL] [Abstract][Full Text] [Related]
17. α-Thalassemia syndromes in the United Arab Emirates.
Baysal E
Hemoglobin; 2011; 35(5-6):574-80. PubMed ID: 22074123
[TBL] [Abstract][Full Text] [Related]
18. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis.
Fucharoen S; Fucharoen G; Sae-ung N; Sanchaisuriya K
Blood Cells Mol Dis; 2007; 39(2):195-8. PubMed ID: 17587614
[TBL] [Abstract][Full Text] [Related]
19. Molecular characterization and origins of Hb Constant Spring and Hb Paksé in Southeast Asian populations.
Singsanan S; Fucharoen G; Savongsy O; Sanchaisuriya K; Fucharoen S
Ann Hematol; 2007 Sep; 86(9):665-9. PubMed ID: 17589844
[TBL] [Abstract][Full Text] [Related]
20. Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR.
Wang W; Yap CH; Loh SF; Tan AS; Lim MN; Prasath EB; Chan ML; Tan WC; Jiang B; Yeo GH; Mathew J; Ho A; Ho SS; Wong PC; Choolani MA; Chong SS
Reprod Biomed Online; 2010 Nov; 21(5):642-8. PubMed ID: 20864413
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
