Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Thanusak Tatu"'
Autor:
Thanusak Tatu, Denis Sweatman
Publikováno v:
Journal of Laboratory Physicians, Vol 10, Iss 02, Pp 214-220 (2018)
BACKGROUND: One-tube osmotic fragility test (OFT) is widely used for screening thalassemia traits. Interobserver variation may occur with 0.36% NaCl-based OFT due to the naked eye result reading style. PURPOSE: The purpose of this study was to establ
Externí odkaz:
https://doaj.org/article/ef55703bc27d4e7191eb3687d9962cbd
Publikováno v:
Journal of Associated Medical Sciences, Vol 30, Iss 1, Pp S62-S62 (2015)
Externí odkaz:
https://doaj.org/article/8f7a2273fb4b443b9667347baf1fb6d0
Autor:
Lamplimas Tangpan, Thanusak Tatu
Publikováno v:
Journal of Associated Medical Sciences, Vol 48, Iss 2, Pp 88-88 (2015)
Introduction : Previous statistical analyses have demonstrated linkage disequilibrium of βE-allele and surrounding in-cis sequences. Objective : To confirm the linkage disequilibrium of βE-allele and surrounding in-cis sequences. Materials and Me
Externí odkaz:
https://doaj.org/article/3190ab804ad94981a3b6c6bf0b6220e9
Publikováno v:
Journal of Associated Medical Sciences, Vol 30, Iss 2, Pp 88-88 (2015)
Externí odkaz:
https://doaj.org/article/948ce82b68e34eed8167092579afe21e
Autor:
Thanusak Tatu, Patcharaporn Lertkham
Publikováno v:
Journal of Associated Medical Sciences, Vol 39, Iss 2, Pp 2-2 (2015)
Externí odkaz:
https://doaj.org/article/d93f949e47274ca3821cc42a5c604504
Autor:
Wibhasiri Srisuwan, Thanusak Tatu
Publikováno v:
Journal of Associated Medical Sciences, Vol 46, Iss 1, Pp 22-22 (2013)
Background: Conventional diagnostic strategy for thalassemia carriers is time-consuming and requires many types of laboratory tests. Objective : To demonstrate the possibility of a combination of MCV or MCH and a PCR-based technique in identifying
Externí odkaz:
https://doaj.org/article/c57f3064debe4cf49d40a811f1707378
Publikováno v:
Journal of Associated Medical Sciences, Vol 44, Iss 1, Pp 17-17 (2011)
HbE/βO-thalassemia is the syndrome resulted from compound heterozygosity of HbE and βO-thalassemia alleles. The diagnosis of this condition relies on the detection of types and amounts of hemoglobin together with the evaluation of red blood cell mo
Externí odkaz:
https://doaj.org/article/b44090cc6bf44d7996a0358d41cb59d7
Publikováno v:
Journal of Associated Medical Sciences, Vol 42, Iss 2, Pp 95-95 (2009)
α-thalassemia is characterized by quantitive abnormality of α-globin chain commonly occur in Thailand. Heterozygote of α-thalassemia is clinically asymtomatic, but with modest alteration of hematologic parameters. This report aimed to evaluate the
Externí odkaz:
https://doaj.org/article/3bf6b85ae878467e9d6089451f74ecba
Publikováno v:
Journal of Associated Medical Sciences, Vol 41, Iss 2, Pp 89-89 (2008)
Faculty of Associated Medical Sciences, Chiang Mai university has launched the Community Service Project to provide medical laboratory test, physical therapy, occupational therapy and medical radiology services to the public. Determinations of fastin
Externí odkaz:
https://doaj.org/article/4e7dc7c9525642d1b027d50960de2cee
Autor:
Thanusak Tatu, Tippawadee Jansai, Ekthong Limweeraprajak, Lamplaimas Tangpan, Sasiwan Kerdpoo, Tiemjan Kiewkarnkha
Publikováno v:
Journal of Immunoassay and Immunochemistry. 40:653-661
The monoclonal antibody (mAb) against γ-globin chain clone Thal N/B was produced. It was aimed at measuring the quantity of HbF (α2γ2)-containing red blood cells or F cells by flow cytometry. Howev...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7368cedfe7b1fa93726ccdd9b83be6cb
https://doi.org/10.1080/15321819.2019.1671862
https://doi.org/10.1080/15321819.2019.1671862