Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Vichai Laosombat"'
Autor:
Darin Sosothikul, Samart Pakakasama, Nattee Narkbunnam, Gavivann Veerakul, Su On Chainansamit, Somjai Kanjanapongkul, Surapon Wiangnon, Pattra Thanarattanakorn, Vichai Laosombat, Somporn Wangruangsathit, Rachata Lumkul
Publikováno v:
International Journal of Hematology. 91:850-854
Survivors of childhood acute lymphoblastic leukemia (ALL) are at risk of long-term late effects. Therefore, systematic screenings of the late complications are essential. The objective of this study was to determine the prevalence of late effects of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34773a58cc5c14916b009360e2d247cf
https://doi.org/10.1007/s12185-010-0594-9
https://doi.org/10.1007/s12185-010-0594-9
Autor:
Vichai Laosombat, Supan Fucharoen, Malai Wongchanchailert, Aranya Wiriyasateinkul, Benjamas Sattayasevana
Publikováno v:
European Journal of Haematology. 66:126-129
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2873bec1e733ccbf4dd7ca3111eb896
https://doi.org/10.1111/j.1600-0609.2001.00305.x
https://doi.org/10.1111/j.1600-0609.2001.00305.x
Autor:
Surini Yusoff, Ahmad Hamim Sadewa, Hisahide Nishio, Hans Van Rostenberghe, Hitoshi Ayaki, Hajime Nakamura, Kayoko Saiki, Masafumi Matsuo, Atsuko Takeuchi, Norlelawati A.Talib, Vichai Laosombat, Retno Sutomo, Narazah Mohd Yusoff, Myeong Jin Lee, Keiko Wada
Publikováno v:
Journal of Chromatography B. 828(1):1398-1401
Mutations in the gene encoding UDP-glucuronosyltransferase 1A1 (UGT1A1) may reduce the glucuronidation of estradiol, bilirubin, etc. In the present study, we used a liquid chromatography-tandem mass spectrometry (LC/MS/MS) method to assay the activit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b18c03c645ac3a01719d82c1f6c2472e
https://hdl.handle.net/20.500.14094/90001403
https://hdl.handle.net/20.500.14094/90001403
Autor:
Masafumi Matsuo, Benjamas Sattayasevana, Taku Shirakawa, Kaoru Nishiyama, Waricha Janejindamai, Vichai Laosombat, Vip Viprakasit
Publikováno v:
Blood Cells, Molecules, and Diseases. 34:191-196
Two hundred and twenty-five G6PD-deficient subjects in Songklanagarind Hospital in the south of Thailand comprising 210 males and 15 females were studied. Neonatal jaundice was detected in 85% of these patients. Acute hemolysis related to infection w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::126f449df230d5c325a29727f7848d3a
https://doi.org/10.1016/j.bcmd.2004.11.001
https://doi.org/10.1016/j.bcmd.2004.11.001
Autor:
Supan Fucharoen, Malai Wongchanchailert, Aranya Wiriyasateinkul, Vichai Laosombat, Benjamas Sattayasevana
Publikováno v:
European Journal of Haematology. 67:100-104
Seventy-eight patients with IVS-1 nt 5, G-C, which is the common mutation of beta+-thalassemia found in the southern part of Thailand, were studied to determine whether it is possible to predict phenotypic severity from genetic factors. The clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::164571768bca6d4ea21d71652f0a46da
https://doi.org/10.1034/j.1600-0609.2001.t01-1-00431.x
https://doi.org/10.1034/j.1600-0609.2001.t01-1-00431.x
Autor:
Aranya Wiriyasateinkul, Benjamas Sattayasevana, Supan Fucharoen, Vichai Laosombat, Malai Wongchanchailert
Publikováno v:
European Journal of Haematology. 66:126-129
Forty-one patients with codon 17, A-T mutation of beta-thalassemia, which is commonly found in Thailand, were studied to determine whether it is possible to predict phenotypic severity from genetic factors. The clinical phenotype of homozygotes for c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c59b520786884319a848d1dbc43ed790
https://doi.org/10.1034/j.1600-0609.2001.00305.x
https://doi.org/10.1034/j.1600-0609.2001.00305.x
Publikováno v:
Hemoglobin. 25:383-389
We report a Thai boy with a compound heterozygosity for the alpha2 polyadenylation signal mutation (AATAAA--AATA--) and alpha0-thalassemia (--SEA), who suffered from Hb H disease with more severe clinical symptoms than those usually observed with del
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2265659bdcfe0de931afde18aee3f7a4
https://doi.org/10.1081/hem-100107875
https://doi.org/10.1081/hem-100107875
Autor:
Philip G. Board, Nunghathai Sawasdee, Sasichai Kangsadalampai, Vichai Laosombat, Gareth Chelvanayagam, Pa-thai Yenchitsomanus
Publikováno v:
European Journal of Haematology. 65:279-284
The molecular defects of the factor XIII A subunit gene were studied in a patient with factor XIII deficiency. Mutation analysis was performed on amplified DNA from each exon of this gene by single-strand conformation polymorphism (SSCP) and DNA sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6941d5f7f9ba2c59bc97de6a71a12760
https://doi.org/10.1034/j.1600-0609.2000.065004279.x
https://doi.org/10.1034/j.1600-0609.2000.065004279.x
Autor:
Pornsak Dissaneewate, Suchitra Thongmak, Vichai Laosombat, Malai Wongchanchailert, Punnee Vasikananont, Supachai Janjindamai, Porpimol Prukprasert, Prayong Vachvanichsanong
Publikováno v:
Infectious Diseases in Clinical Practice. 11:211-213
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6869887a9f3d0ec66f6f133ed83e8063
https://doi.org/10.1097/00019048-200205000-00005
https://doi.org/10.1097/00019048-200205000-00005
Autor:
Aranya Wiriyasateinkul, Vichai Laosombat, Malai Wongchanchailert, Somchai Watanaarepornchai, Benjamas Sattayasevana
Publikováno v:
Medical and Pediatric Oncology. 38:266-268
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55ced204751b7ac64f12375c927cf3b5
https://doi.org/10.1002/mpo.1321
https://doi.org/10.1002/mpo.1321