Chinchang W - Search Results

1

Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder.

Viprakasit V, Vathesathokit P, Chinchang W, Tachavanich K, Pung-Amritt P, Wimhurst VL, Yenchitsomanus PT, Merryweather-Clarke AT, Tanphaichitr VS. Viprakasit V, et al. Among authors: chinchang w. Eur J Haematol. 2004 Jul;73(1):43-9. doi: 10.1111/j.1600-0609.2004.00246.x. Eur J Haematol. 2004. PMID: 15182337

2

Hb Woodville, a rare alpha-globin variant, caused by codon 6 mutation of the alpha1 gene.

Viprakasit V, Chinchang W, Chotimarat P. Viprakasit V, et al. Among authors: chinchang w. Eur J Haematol. 2006 Jan;76(1):79-82. doi: 10.1111/j.0902-4441.2005.t01-1-EJH2334.x. Eur J Haematol. 2006. PMID: 16343275

3

Common origin of a rare beta-globin initiation codon mutation (ATG-->AGG) in Asians.

Viprakasit V, Chinchang W, Suwanthol L, Tanphaichitr VS. Viprakasit V, et al. Among authors: chinchang w. Clin Lab Haematol. 2005 Dec;27(6):409-15. doi: 10.1111/j.1365-2257.2005.00734.x. Clin Lab Haematol. 2005. PMID: 16307546

4

Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia.

Viprakasit V, Tanphaichitr VS, Chinchang W, Sangkla P, Weiss MJ, Higgs DR. Viprakasit V, et al. Among authors: chinchang w. Blood. 2004 May 1;103(9):3296-9. doi: 10.1182/blood-2003-11-3957. Epub 2004 Jan 8. Blood. 2004. PMID: 14715623 Free article.

5

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. Viprakasit V, et al. Among authors: chinchang w. Am J Hematol. 2004 Mar;75(3):157-63. doi: 10.1002/ajh.10479. Am J Hematol. 2004. PMID: 14978697 Free article.

6

Identification of Hb Q-India (alpha64 Asp-->His) in Thailand.

Viprakasit V, Chinchang W, Pung-Amritt P, Tanphaichitr VS. Viprakasit V, et al. Among authors: chinchang w. Hematology. 2004 Apr;9(2):151-5. doi: 10.1080/10245330310001652455. Hematology. 2004. PMID: 15203872 Free article.

7

Acute haemolytic crisis in a Thai patient with homozygous haemoglobin Constant Spring (Hb CS/CS): a case report.

Viprakasit V, Veerakul G, Sanpakit K, Pongtanakul B, Chinchang W, Tanphaichitr VS. Viprakasit V, et al. Among authors: chinchang w. Ann Trop Paediatr. 2004 Dec;24(4):323-8. doi: 10.1179/027249304225019145. Ann Trop Paediatr. 2004. PMID: 15720889

8

A rare association of alphaO-thalassemia (--SEA) and an initiation codon mutation (ATG-->A-G) of the alpha2 gene causes Hb H disease in Thailand.

Viprakasit V, Chinchang W, Glomglao W, Tanphaichitr VS. Viprakasit V, et al. Among authors: chinchang w. Hemoglobin. 2005;29(3):235-40. doi: 10.1081/hem-200066339. Hemoglobin. 2005. PMID: 16116675

9

Molecular analysis of unknown beta-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with beta-thalassemias and beta-globin variants.

Chinchang W, Viprakasit V, Pung-Amritt P, Tanphaichitr VS, Yenchitsomanus PT. Chinchang W, et al. Clin Biochem. 2005 Nov;38(11):987-96. doi: 10.1016/j.clinbiochem.2005.07.013. Epub 2005 Sep 2. Clin Biochem. 2005. PMID: 16139831

10

Two independent origins of Hb Dhonburi (Neapolis) [beta 126 (H4) Val-->Gly]: an electrophoretically silent hemoglobin variant.

Viprakasit V, Chinchang W. Viprakasit V, et al. Among authors: chinchang w. Clin Chim Acta. 2007 Feb;376(1-2):179-83. doi: 10.1016/j.cca.2006.08.016. Epub 2006 Aug 17. Clin Chim Acta. 2007. PMID: 17007829

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