Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Kritsada, Singha"'
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:
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:
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:
Chayada Soontornpanawet, Kritsada Singha, Hataichanok Srivorakun, Wanicha Tepakhan, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
PeerJ; May2023, p1-18, 18p
Publikováno v:
Annals of Hematology. 100:1953-1963
The δ-globin gene defects are clinically silent but interaction with β-thalassemia can lead to a misdiagnosis of β-thalassemia carrier. We report an extensive molecular characterization of δ-hemoglobinopathies in Thailand. Study was done on 32,10
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
Publikováno v:
International journal of laboratory hematology. 44(5)
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)
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. Methods A total
Publikováno v:
Journal of Clinical Pathology. 73:511-513
We describe a dominant β-thalassaemia caused by a deletion of G at nucleotide position 364 in exon 3 of the β-globin gene. The heterozygosity of this mutation was found in a 36-year-old Thai patient who had moderate hypochromic microcytic anaemia w