Sura T - Search Results

1

Noonan syndrome, metabolic syndrome and stroke-in-the-young: coincidence, causal or contribution?

Eu-ahsunthornwattana J, Trachoo O, Dejsuphong D, Tunteeratum A, Srichan K, Sura T. Eu-ahsunthornwattana J, et al. Among authors: sura t. J Med Assoc Thai. 2010 Sep;93(9):1084-7. J Med Assoc Thai. 2010. PMID: 20873082

2

Molecular characterization of hereditary persistence of fetal hemoglobin in the Karen people of Thailand.

Trachoo O, Sura T, Sakuntabhai A, Singhasivanon P, Krudsood S, Phimpraphi W, Krasaesub S, Chanjarunee S, Looareesuwan S. Trachoo O, et al. Among authors: sura t. Hemoglobin. 2003 May;27(2):97-104. doi: 10.1081/hem-120021542. Hemoglobin. 2003. PMID: 12779271

3

Oculopharyngodistal myopathy in a Thai family.

Witoonpanich R, Phankhian S, Sura T, Lertrit P, Phudhichareonrat S. Witoonpanich R, et al. Among authors: sura t. J Med Assoc Thai. 2004 Dec;87(12):1518-21. J Med Assoc Thai. 2004. PMID: 15822551

4

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. Ann Hematol. 2007 Sep;86(9):659-63. doi: 10.1007/s00277-007-0303-9. Epub 2007 May 15. Ann Hematol. 2007. PMID: 17503046

5

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. 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

6

Ehlers-Danlos syndrome type IV with gastric adenocarcinoma.

Kanechorn Na Ayuthaya R, Patthamapasphong N, Sura T, Niumpradit N, Trachoo O. Kanechorn Na Ayuthaya R, et al. Among authors: sura t. J Med Assoc Thai. 2008;91 Suppl 1:S166-71. J Med Assoc Thai. 2008. PMID: 18672610

7

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. Dis Markers. 2008;25(2):115-21. doi: 10.1155/2008/521568. Dis Markers. 2008. PMID: 18957722 Free PMC article.

8

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. 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

9

Congestive heart failure with rhabdomyolysis and acute renal failure in a manifesting female carrier of Duchenne muscular dystrophy with duplication of dystrophin gene.

Tunteeratum A, Witoonpanich R, Phudhichareonrat S, Eu-ahsunthornwattana J, Pingsuthiwong S, Srichan K, Sura T. Tunteeratum A, et al. Among authors: sura t. J Clin Neuromuscul Dis. 2009 Sep;11(1):49-53. doi: 10.1097/CND.0b013e3181adcda7. J Clin Neuromuscul Dis. 2009. PMID: 19730022

10

Association of estrogen receptor-alpha single-nucleotide polymorphism (codon 594 G-->A) and Thai patients affected by knee osteoarthritis.

Tawonsawatruk T, Trachoo O, Channoom T, Sura T, Eu-ahsunthornwattana J, Woratanarat P, Wajanavisit W. Tawonsawatruk T, et al. Among authors: sura t. J Med Assoc Thai. 2009 Dec;92 Suppl 6:S45-50. J Med Assoc Thai. 2009. PMID: 20128071

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

107 results

Search Page

Filters