Busabaratana M - Search Results

1

Sensitivity and frequencies of dystrophin gene mutations in Thai DMD/BMD patients as detected by multiplex PCR.

Sura T, Eu-ahsunthornwattana J, Pingsuthiwong S, Busabaratana M. Sura T, et al. Among authors: busabaratana m. Dis Markers. 2008;25(2):115-21. doi: 10.1155/2008/521568. Dis Markers. 2008. PMID: 18957722 Free PMC article.

2

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. Sura T, et al. Among authors: busabaratana m. Ann Hematol. 2007 Sep;86(9):659-63. doi: 10.1007/s00277-007-0303-9. Epub 2007 May 15. Ann Hematol. 2007. PMID: 17503046

3

Frequencies of spinocerebellar ataxia subtypes in Thailand: window to the population history?

Sura T, Eu-Ahsunthornwattana J, Youngcharoen S, Busabaratana M, Dejsuphong D, Trachoo O, Theerasasawat S, Tunteeratum A, Noparutchanodom C, Tunlayadechanont S. Sura T, et al. Among authors: busabaratana m. J Hum Genet. 2009 May;54(5):284-8. doi: 10.1038/jhg.2009.27. Epub 2009 Mar 27. J Hum Genet. 2009. PMID: 19329990

4

Analysis of exon 8 of ATP7B gene in Thai patients with Wilson disease.

Keandaungjuntr J, Busabaratana M, Kositchaiwat C, Sura T, Pulkes T. Keandaungjuntr J, et al. Among authors: busabaratana m. J Med Assoc Thai. 2011 Oct;94(10):1184-8. J Med Assoc Thai. 2011. PMID: 22145502

5

Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population.

Angchaisuksiri P, Pingsuthiwong S, Aryuchai K, Busabaratana M, Sura T, Atichartakarn V, Sritara P. Angchaisuksiri P, et al. Among authors: busabaratana m. Am J Hematol. 2000 Oct;65(2):119-22. doi: 10.1002/1096-8652(200010)65:2<119::aid-ajh5>3.0.co;2-8. Am J Hematol. 2000. PMID: 10996828 Free article.

6

Prevalence of the C677T methylenetetra- hydrofolate reductase mutation in Thai patients with deep vein thrombosis.

Angchaisuksiri P, Pingsuthiwong S, Sura T, Aryuchai K, Busabaratana M, Atichartakarn V. Angchaisuksiri P, et al. Among authors: busabaratana m. Acta Haematol. 2000;103(4):191-6. doi: 10.1159/000041048. Acta Haematol. 2000. PMID: 11014892

7

Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease.

Sura T, Busabaratana M, Youngcharoen S, Wisedpanichkij R, Viprakasit V, Trachoo O. Sura T, et al. Among authors: busabaratana m. Eur J Haematol. 2007 Sep;79(3):251-4. doi: 10.1111/j.1600-0609.2007.00907.x. Epub 2007 Jul 26. Eur J Haematol. 2007. PMID: 17655700

8

Mutation and haplotype analysis of oculopharyngeal muscular dystrophy in Thai patients.

Pulkes T, Papsing C, Busabaratana M, Dejthevaporn C, Witoonpanich R. Pulkes T, et al. Among authors: busabaratana m. J Clin Neurosci. 2011 May;18(5):674-7. doi: 10.1016/j.jocn.2010.08.020. J Clin Neurosci. 2011. PMID: 21316245

9

Association between apolipoprotein E genotypes and Parkinson's disease.

Pulkes T, Papsing C, Mahasirimongkol S, Busabaratana M, Kulkantrakorn K, Tiamkao S. Pulkes T, et al. Among authors: busabaratana m. J Clin Neurosci. 2011 Oct;18(10):1333-5. doi: 10.1016/j.jocn.2011.01.028. Epub 2011 Jul 22. J Clin Neurosci. 2011. PMID: 21782446

10

Frequencies of LRRK2 variants in Thai patients with Parkinson's disease: evidence for an R1628P founder.

Pulkes T, Papsing C, Mahasirimongkol S, Busabaratana M, Kulkantrakorn K, Tiamkao S. Pulkes T, et al. Among authors: busabaratana m. J Neurol Neurosurg Psychiatry. 2011 Oct;82(10):1179-80. doi: 10.1136/jnnp.2009.194597. Epub 2010 Jun 22. J Neurol Neurosurg Psychiatry. 2011. PMID: 20571044 No abstract available.

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