Zobrazeno 1 - 10
of 281
pro vyhledávání: '"Supan Fucharoen"'
Autor:
Kritsada Singha, Anupong Pansuwan, Mattanee Chewasateanchai, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract High Hb F determinants are genetic defects associated with increased expression of hemoglobin F in adult life, classified as deletional and non-deletional forms. We report the first description of non-deletional hereditary persistence of fet
Externí odkaz:
https://doaj.org/article/388557aaf6c94b57acef760bf4658ae0
Autor:
Rossarin Karnpean, Nawinda Vanichakulthada, Wanwisa Suwannaloet, Ruttiya Thongrung, Sanita Singsanan, Nattapol Prakobkaew, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Anemia is a major public health problem in many areas of Southeast Asia. Ascertaining anemia and defining its underlying causes is essential for providing appropriate care, management, and establishment of a control program. Limited studies
Externí odkaz:
https://doaj.org/article/0fec3cab22554e5d859e1d0ed63da5aa
Autor:
Chayada Soontornpanawet, Kritsada Singha, Hataichanok Srivorakun, Wanicha Tepakhan, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
PeerJ, Vol 11, p e15308 (2023)
Background β0-thalassemia deletion removing 5´β-globin promoter usually presents phenotype with high hemoglobin (Hb) A2 and Hb F levels. We report the molecular characteristics and phenotype-genotype correlation in a large cohort of the β0-thalas
Externí odkaz:
https://doaj.org/article/47bd68c5bc5f4225b0178f6ffe7f917e
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:
Thinzar Win Pyae, Kanokwan Sanchaisuriya, Surasak Athikamanon, Pattara Sanchaisuriya, Hataichanok Srivorakun, Attawut Chaibunruang, Supan Fucharoen
Publikováno v:
PLoS ONE, Vol 18, Iss 6, p e0287527 (2023)
BackgroundAnemia is a globally well-known major public health problem. In Southeast Asia where there is ethnic diversity, both iron deficiency (ID) and inherited hemoglobin disorders (IHDs) are prevalent and are considered to be the major factors con
Externí odkaz:
https://doaj.org/article/f48026c8841b4c479de1a3fabc30fac8
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:
Hataichanok Srivorakun, Wachiraporn Thawinan, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Supan Fucharoen
Publikováno v:
Archives of Medical Science, Vol 18, Iss 1, Pp 112-120 (2020)
Introduction Elevated hemoglobin (Hb) A 2 is an important diagnostic marker for β-thalassemia carriers. However, diagnosis of cases with borderline Hb A 2 may be problematic. We described the molecular characteristics found in a large cohort of Thai
Externí odkaz:
https://doaj.org/article/015a53f17027405c83609f037b462887
Autor:
Jutatip Jamnok, Kanokwan Sanchaisuriya, Pattara Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen, Faruk Ahmed
Publikováno v:
BMC Public Health, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Background Anaemia and iron deficiency (ID) affect women of reproductive age globally and considered to be a major public health problem in developing countries. This study determines the prevalence of anaemia and ID among women of reproduct
Externí odkaz:
https://doaj.org/article/358e8e881520416da99cc17e07e65b31
Publikováno v:
PLoS ONE, Vol 17, Iss 4, p e0267832 (2022)
BackgroundIdentification of α0-thalassemia (SEA and THAI deletions) is essential in preventing and controlling of severe thalassemia diseases. We have developed the LAMP colorimetric assays for the detection of these two thalassemia defects and vali
Externí odkaz:
https://doaj.org/article/b261a6dfc0ad4f018298f75e15af959b