Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Arunee Phusua"'
Autor:
Sirichai Srichairatanakool, Chatree Chai-Adisaksopha, Adisak Tantiworawit, Arunee Phusua, Pimlak Charoenkwan
Publikováno v:
American Journal of Case Reports; 5/10/2024, Vol. 25, p1-5, 5p
Autor:
Vip Viprakasit, Pimlak Charoenkwan, Chupong Ittiwut, Vorasuk Shotelersuk, Wanna Chetruengchai, Arunee Phusua, Kanda Fanhchaksai, Monthana Juntharaniyom, Chureerat Phokaew, Tanu Tangsricharoen, Rungrote Natesirinilkul
Publikováno v:
British Journal of Haematology. 194:626-634
Mutations in the KLF1 gene, which encodes a transcription factor playing a role in erythropoiesis, have recently been demonstrated to be a rare cause of hereditary haemolytic anaemia. We described the genotypic and phenotypic spectra of four unrelate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7a60d7f4bad8a6e41b9281017fdcf78
https://doi.org/10.1111/bjh.17616
https://doi.org/10.1111/bjh.17616
Autor:
Pimlak Charoenkwan, Kuntharee Traisrisilp, Supatra Sirichotiyakul, Arunee Phusua, Torpong Sanguansermsri, Theera Tongsong
Publikováno v:
Fetal diagnosis and therapy.
Introduction: Prenatal diagnosis of thalassemia disease was usually based on invasive technique. Noninvasive diagnosis using cell-free fetal DNA (cff-DNA) was described with various laboratory techniques. The aim of this study was to identify the per
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b982d7c2bbd6bcab8658855e7fed2daf
https://pubmed.ncbi.nlm.nih.gov/36574763
https://pubmed.ncbi.nlm.nih.gov/36574763
Autor:
Phumin Chaweephisal, Arunee Phusua, Supatra Sirichotiyakul, Pimlak Charoenkwan, Kanda Fanhchaksai
Publikováno v:
Blood Cells, Molecules, and Diseases. 74:13-17
Introduction Identification of beta-thalassemia carrier in prenatal screening relies on the elevated Hb A2 level. Borderline Hb A2 levels pose a diagnostic challenge. We determined the HBB genotypes in subjects with borderline Hb A2 in northern Thail
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b493a0fae6a160c794e8d342813d9a92
https://doi.org/10.1016/j.bcmd.2018.10.002
https://doi.org/10.1016/j.bcmd.2018.10.002
Autor:
Pimlak Charoenkwan, Vorasuk Shotelersuk, Chupong Ittiwut, Chane Choed-Amphai, Kanya Suphapeetiporn, Arunee Phusua
Publikováno v:
Journal of pediatric hematology/oncology. 43(5)
Hemoglobin (Hb) H/Constant Spring disease is a common nondeletional Hb H disease, typically causing a more severe phenotype than the deletional Hb H disease counterpart. Hb Tak, resulting from a dinucleotide insertion (+AC) at codon 146 of beta-globi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f306d78ad4e6593e2db5b7eac551a0d2
https://pubmed.ncbi.nlm.nih.gov/32925409
https://pubmed.ncbi.nlm.nih.gov/32925409
Autor:
Rattika Saetung, Pimlak Charoenkwan, Sudjai Suanta, Kanda Fanhchaksai, Torpong Sanguansermsri, Arunee Phusua, Supatra Sirichotiyakul
Publikováno v:
International Journal of Hematology. 106:757-764
High-resolution melting (HRM) analysis is a rapid mutation analysis which assesses the pattern of reduction of fluorescence signal after subjecting the amplified PCR product with saturated fluorescence dye to an increasing temperature. We used HRM an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a67bbdc5e77cc24927c0c73824b8a11
https://doi.org/10.1007/s12185-017-2306-1
https://doi.org/10.1007/s12185-017-2306-1
Publikováno v:
Pediatric bloodcancerREFERENCES. 67(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09c94f1d2982ef03f2bd8e0021f68c52
https://pubmed.ncbi.nlm.nih.gov/31930713
https://pubmed.ncbi.nlm.nih.gov/31930713
Autor:
Pitipong Srisittipoj, Torpong Sanguansermsri, Arunee Phusua, Pimlak Charoenkwan, Sudjai Suanta, Kanittha Mankhemthong
Publikováno v:
International journal of hematology. 110(4)
Molecular analysis of globin genes is an essential process for prenatal diagnosis (PND) of severe thalassemia. This study aimed to describe the molecular characteristics of thalassemia and hemoglobin (Hb) variants in PND program in northern Thailand.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d991371d2b03b29c7bf2a7c56861375
https://pubmed.ncbi.nlm.nih.gov/31240559
https://pubmed.ncbi.nlm.nih.gov/31240559
Autor:
Phumin, Chaweephisal, Arunee, Phusua, Kanda, Fanhchaksai, Supatra, Sirichotiyakul, Pimlak, Charoenkwan
Publikováno v:
Blood cells, moleculesdiseases. 74
Identification of beta-thalassemia carrier in prenatal screening relies on the elevated Hb ABlood samples with Hb AHBB mutations were found in 298 (98.7%) of 302 samples with Hb AHBB mutations in northern Thais with borderline Hb A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22015ffb67f9df33b30bfc474efeb1a5
https://pubmed.ncbi.nlm.nih.gov/30309760
https://pubmed.ncbi.nlm.nih.gov/30309760
Autor:
Sasinee Hantrakool, Chatree Chai-Adisaksopha, Suree Lekawanvijit, Thanawat Rattanathammethee, Pimlak Charoenkwan, Noppamas Kumpunya, Adisak Tantiworawit, Ratchanoo Tongphung, Lalita Norasetthada, Arunee Phusua, Ornkamon Wongtagan, Ekarat Rattarittamrong
Publikováno v:
Hematology (Amsterdam, Netherlands). 23(9)
Objectives The primary objective was to determine the prevalence of calreticulin (CALR) mutation in patients with non-JAK2V617F mutated essential thrombocythemia (ET). The secondary objectives were to evaluate the accuracy of CALR mutation analysis b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::887082a8aa6d7a711cd455809077a4f3
https://pubmed.ncbi.nlm.nih.gov/29521158
https://pubmed.ncbi.nlm.nih.gov/29521158