Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Supawadee Yamsri"'
Autor:
Kritsada Singha, Supawadee Yamsri, Attawut Chaibunruang, Hataichanok Srivorakun, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Abstract Background To evaluate whether the quantification of fetal hemoglobin (Hb) Bart’s is useful for differentiation of α-thalassemia syndromes in the fetus and to characterize the fetal anemia associated with fetal α-hemoglobinopathy. Method
Externí odkaz:
https://doaj.org/article/a0e818dba38e45cba005fe6b1ba74a5e
Autor:
Kritsada Singha, Supawadee Yamsri, Attawut Chaibunruang, Hataichanok Srivorakun, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
PLoS ONE, Vol 18, Iss 4, p e0283051 (2023)
ObjectiveTo determine the frequency and etiology of unnecessary prenatal diagnosis for hemoglobinopathies during 12 years of services at a single university center in Thailand.MethodsWe conducted a retrospective cohort analysis of prenatal diagnosis
Externí odkaz:
https://doaj.org/article/d4507e814cc74a38a6d0825607a1b41d
Autor:
Siriyakorn Chansai, Supawadee Yamsri, Supan Fucharoen, Goonnapa Fucharoen, Nattiya Teawtrakul
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 14, Iss 1 (2022)
Introduction: Extramedullary hematopoiesis (EMH) is one of the main complications in patients with thalassemia in compensation for the underlying ineffective erythropoiesis. This study aimed to evaluate the association between ineffective erythropoie
Externí odkaz:
https://doaj.org/article/fea35046cb5146d4862ca39c25fe4b90
Autor:
Sumalai Dechyotin, Kittipong Sakunthai, Noppmats Khemtonglang, Supawadee Yamsri, Kanokwan Sanchaisuriya, Kriengkrai Kitcharoen, Suttiphan Kitcharoen
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 13, Iss 1 (2021)
Introduction: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common X-linked enzymopathy, highly prevalent in areas where malaria is or has been endemic. Prevalence of G6PD deficiency and characterization of G6PD variants in females
Externí odkaz:
https://doaj.org/article/a00d0f1af45e496c89ae2b25ec74573e
Autor:
Paramee Phanrahan, Supawadee Yamsri, Nattiya Teawtrakul, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Supan Fucharoen
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 11, Iss 1 (2019)
Background: The finding of many Thai Hb E-β0-thalassemia patients with non-transfusion dependent thalassemia (NTDT) phenotype without co-inheritance of α-thalassemia has prompted us to investigate the existence of other genetic modifying factors.
Externí odkaz:
https://doaj.org/article/cb81ad789b944d488bac3cc31326e738
Autor:
Anupong Pansuwan, Duangrudee Changtrakul, Attawut Chaibunruang, Supawadee Yamsri, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
International Journal of Laboratory Hematology. 44:666-672
Hemoglobinopathies are major public health problems worldwide. Accurate laboratory diagnosis of the carrier is essential, which includes initial screening, Hb analysis, and DNA analysis. For the first time, we have developed a single-tube quality con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::554276940dea49ac84c974d318f6a95c
https://doi.org/10.1111/ijlh.13775
https://doi.org/10.1111/ijlh.13775
Publikováno v:
Medical Science Monitor Basic Research. 28
BACKGROUND Mutations in the FLT3 gene are associated with acute myeloid leukemia (AML). FLT3 mutations have been identified in approximately 30% of de novo AML patients, particularly those with typical karyotype and inferior prognosis. Therefore, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::508bdb8be2c2f99677f0f5abe539c878
https://doi.org/10.12659/msmbr.937446
https://doi.org/10.12659/msmbr.937446
Autor:
Sanita Singsanan, Supawadee Yamsri, Kanjana Pangjit, Phairo Saenwang, Rossarin Karnpean, Supan Fucharoen
Publikováno v:
Genetic testing and molecular biomarkers. 26(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee9cd3a7dd87e0fadc4e4d5dcc57c668
https://pubmed.ncbi.nlm.nih.gov/35763384
https://pubmed.ncbi.nlm.nih.gov/35763384
Publikováno v:
Annals of Hematology. 100:2863-2865
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fe608f61b6946efc29fb39fe0fd1ae3
https://doi.org/10.1007/s00277-021-04582-0
https://doi.org/10.1007/s00277-021-04582-0
Autor:
Hataichanok Srivorakun, Goonnapa Fucharoen, Supawadee Yamsri, Kritsada Singha, Bounpalisone Souvanlasy, Attawut Chaibunruang, Supan Fucharoen
Publikováno v:
International Journal of Laboratory Hematology. 43:500-505
Introduction A high frequency of β-thalassemia in Lao People's Democratic Republic necessitates the importance of complete molecular data before a prevention and control program could be established. Limited data are available for Lao PDR. We have n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::666ad5710cf964ec51b00cef9a1f2888
https://doi.org/10.1111/ijlh.13406
https://doi.org/10.1111/ijlh.13406