BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

823 related articles for article (PubMed ID: 14978697)

  • 1. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
    Viprakasit V; Tanphaichitr VS; Veerakul G; Chinchang W; Petrarat S; Pung-Amritt P; Higgs DR
    Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N; Pinmuang-Ngam C; Fucharoen G; Fucharoen S
    Fetal Diagn Ther; 2007; 22(4):264-8. PubMed ID: 17369692
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Harteveld CL; Versteegh FG; Kok PJ; van Rooijen-Nijdam IH; van Delft P; Giordano PC
    Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
    Li D; Liao C; Li J; Xie X; Huang Y; Zhong H
    Haematologica; 2006 May; 91(5):649-51. PubMed ID: 16627247
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Two independent origins of Hb Dhonburi (Neapolis) [beta 126 (H4) Val-->Gly]: an electrophoretically silent hemoglobin variant.
    Viprakasit V; Chinchang W
    Clin Chim Acta; 2007 Feb; 376(1-2):179-83. PubMed ID: 17007829
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dominantly Inherited beta-Thalassemia.
    Efremov GD
    Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method.
    Sura T; Trachoo O; Viprakasit V; Vathesatogkit P; Tunteeratum A; Busabaratana M; Wisedpanichkij R; Isarangkura P
    Ann Hematol; 2007 Sep; 86(9):659-63. PubMed ID: 17503046
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular mechanisms of thalassemia in southeast Asia.
    Winichagoon P; Fucharoen S; Wilairat P; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():235-40. PubMed ID: 8629113
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2).
    Martin G; Villegas A; González FA; Ropero P; Hojas R; Polo M; Mateo M; Salvador M; Benavente C
    Hemoglobin; 2005; 29(2):113-7. PubMed ID: 15921163
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Variable and often severe phenotypic expression in patients with the α-thalassemic variant Hb Agrinio [α29(B10)Leu→Pro (α2)].
    Traeger-Synodinos J; Douna V; Papassotiriou I; Stamoulakatou A; Ladis V; Siahanidou T; Fylaktou I; Kanavakis E
    Hemoglobin; 2010; 34(5):430-8. PubMed ID: 20854116
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. 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]  

    [Next]    [New Search]
    of 42.