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Items: 1 to 20 of 104

1.

Detection of the hemoglobin E mutation using the color complementation assay: application to complex genotyping.

Embury SH, Kropp GL, Stanton TS, Warren TC, Cornett PA, Chehab FF.

Blood. 1990 Aug 1;76(3):619-23.

2.

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.

PMID:
12694166
3.

Molecular basis of HbE-beta-thalassemia and the origin of HbE in northeast Thailand: identification of one novel mutation using amplified DNA from buffy coat specimens.

Fucharoen G, Fucharoen S, Jetsrisuparb A, Fukumaki Y.

Biochem Biophys Res Commun. 1990 Jul 31;170(2):698-704.

PMID:
1974422
4.

Differentiation of homozygous hemoglobin E from compound heterozygous hemoglobin E-beta O-thalassemia by hemoglobin E mutation analysis.

Johnson JP, Vichinsky E, Hurst D, Camber A, Lubin B, Louie E.

J Pediatr. 1992 May;120(5):775-9.

PMID:
1374466
5.

Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families.

Fucharoen S, Sanchaisuriya K, Fucharoen G, Panyasai S, Devenish R, Luy L.

Haematologica. 2003 Oct;88(10):1092-8.

7.

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. Epub 2002 Jul 3.

PMID:
12185510
8.
9.

A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosis.

Fucharoen S, Fucharoen G, Ratanasiri T, Jetsrisuparb A, Fukumaki Y.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:278-81.

PMID:
8629124
10.

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.

PMID:
15693792
11.

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. Epub 2003 Aug 30.

PMID:
12955472
12.

Multiplex minisequencing screen for common Southeast Asian and Indian beta-thalassemia mutations.

Wang W, Kham SK, Yeo GH, Quah TC, Chong SS.

Clin Chem. 2003 Feb;49(2):209-18.

13.

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.

PMID:
8629117
15.

Molecular and hematological characterization of hemoglobin Hope/hemoglobin E and hemoglobin Hope/alpha-thalassemia 2 in Thai patients.

Chunpanich S, Fucharoen S, Sanchaisuriya K, Fucharoen G, Kam-itsara K.

Lab Hematol. 2004;10(4):215-20.

PMID:
15697092
16.

Mass spectrometry-based detection of hemoglobin E mutation by allele-specific base extension reaction.

Tsang JC, Charoenkwan P, Chow KC, Jin Y, Wanapirak C, Sanguansermsri T, Lo YM, Chiu RW.

Clin Chem. 2007 Dec;53(12):2205-9. Epub 2007 Oct 19.

17.

Simultaneous PCR detection of beta - thalassemia and alpha - thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome.

Siriratmanawong N, Fucharoen G, Sanchaisuriya K, Ratanasiri T, Fucharoen S.

Clin Biochem. 2001 Jul;34(5):377-80.

PMID:
11522274
18.

Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.

Srivorakun H, Fucharoen G, Sae-Ung N, Sanchaisuriya K, Ratanasiri T, Fucharoen S.

Eur J Haematol. 2009 Jul;83(1):57-65. doi: 10.1111/j.1600-0609.2009.01245.x. Epub 2009 Feb 17.

PMID:
19226360
19.
20.

Evaluation of the BeTha gene 1 kit for the qualitative detection of the eight most common Mediterranean beta-thalassemia mutations.

Ugozzoli LA, Lowery JD, Reyes AA, Lin CI, Re A, Locati F, Galanello R, Macioni L, Maggio A, Giambona A, Loutradi A, Boussiou M, Wallace RB.

Am J Hematol. 1998 Nov;59(3):214-22.

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