Yenchitsomanus P - Search Results

1

Genotype and phenotype of haemophilia A in Thai patients.

Yenchitsomanus P, Akkarapatumwong V, Pung-Amritt P, Intorasoot S, Thanootarakul P, Oranwiroon S, Veerakul G, Mahasandana C. Yenchitsomanus P, et al. Haemophilia. 2003 Mar;9(2):179-86. doi: 10.1046/j.1365-2516.2003.00729.x. Haemophilia. 2003. PMID: 12614369

2

A novel Asn344 deletion in the core domain of coagulation factor XIII A subunit: its effects on protein structure and function.

Kangsadalampai S, Chelvanayagam G, Baker RT, Yenchitsomanus P, Pung-amritt P, Mahasandana C, Board PG. Kangsadalampai S, et al. Among authors: yenchitsomanus p. Blood. 1998 Jul 15;92(2):481-7. Blood. 1998. PMID: 9657747 Free article.

3

Mutations of the factor VIII gene in thai hemophilia A patients.

Akkarapatumwong V, Oranwiroon S, Pung-amritt P, Treesucon A, Thanootarakul P, Veerakul G, Mahasandana C, Panyim S, Yenchitsomanus P. Akkarapatumwong V, et al. Among authors: yenchitsomanus p. Hum Mutat. 2000 Jan;15(1):117-8. doi: 10.1002/(SICI)1098-1004(200001)15:1<117::AID-HUMU27>3.0.CO;2-E. Hum Mutat. 2000. PMID: 10612839

4

Frameshift mutations with severe and moderate clinical phenotypes in Thai hemophilia A patients.

Akkarapatumwong V, Intorasoot S, Oranwiroon S, Thano-Otarakul P, Pung-Amritt P, Veerakul G, Mahasandana C, Panyim S, Yenchitsomanus P. Akkarapatumwong V, et al. Among authors: yenchitsomanus p. Hum Mutat. 2000 Dec;16(6):530-1. doi: 10.1002/1098-1004(200012)16:6<530::AID-HUMU16>3.0.CO;2-3. Hum Mutat. 2000. PMID: 11102988

5

Determination of haemophilia A carrier status by mutation analysis.

Oranwiroon S, Akkarapatumwong V, Pung-Amritt P, Treesucon A, Veerakul G, Mahasandana C, Panyim S, Yenchitsomanus P. Oranwiroon S, et al. Among authors: yenchitsomanus p. Haemophilia. 2001 Jan;7(1):20-5. doi: 10.1046/j.1365-2516.2001.00453.x. Haemophilia. 2001. PMID: 11136376

6

Mutation causing exon 15 skipping and partial exon 16 deletion in factor VIII transcript, and a method for direct mutation detection.

Yenchitsomanus P, Thanootarakul P, Akkarapatumwong V, Oranwiroon S, Pung-Amritt P, Veerakul G, Mahasandana C. Yenchitsomanus P, et al. Haemophilia. 2001 May;7(3):335-8. doi: 10.1046/j.1365-2516.2001.00507.x. Haemophilia. 2001. PMID: 11380640

7

Carrier detection by DNA linkage analysis in eighty Thai hemophilia A families.

Mahasandana C, Pung-Amritt P, Treesucon A, Petrarat S, Veerakul G, Visudhiphan S, Yenchitsomanus PT. Mahasandana C, et al. Among authors: yenchitsomanus pt. J Med Assoc Thai. 2002 Aug;85 Suppl 2:S513-21. J Med Assoc Thai. 2002. PMID: 12403227

8

Anion exchanger 1 mutations associated with distal renal tubular acidosis in the Thai population.

Yenchitsomanus PT, Sawasdee N, Paemanee A, Keskanokwong T, Vasuvattakul S, Bejrachandra S, Kunachiwa W, Fucharoen S, Jittphakdee P, Yindee W, Promwong C. Yenchitsomanus PT, et al. J Hum Genet. 2003;48(9):451-456. doi: 10.1007/s10038-003-0059-6. Epub 2003 Aug 21. J Hum Genet. 2003. PMID: 12938018

9

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: yenchitsomanus pt. Eur J Haematol. 2004 Jul;73(1):43-9. doi: 10.1111/j.1600-0609.2004.00246.x. Eur J Haematol. 2004. PMID: 15182337

10

Trafficking defects of a novel autosomal recessive distal renal tubular acidosis mutant (S773P) of the human kidney anion exchanger (kAE1).

Kittanakom S, Cordat E, Akkarapatumwong V, Yenchitsomanus PT, Reithmeier RA. Kittanakom S, et al. J Biol Chem. 2004 Sep 24;279(39):40960-71. doi: 10.1074/jbc.M405356200. Epub 2004 Jul 13. J Biol Chem. 2004. PMID: 15252044 Free article.

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