Výsledky vyhledávání - "Amphai Phasit"

Akademický článek

Effective screening of hemoglobin Constant Spring and hemoglobin Paksé with several forms of α- and β-thalassemia in an area with a high prevalence and heterogeneity of thalassemia using capillary electrophoresis

Autor: Sitthichai Panyasai, Surada Satthakarn, Amphai Phasit

Publikováno v: Heliyon, Vol 9, Iss 8, Pp e19116- (2023)

Background and aims: We aimed to evaluate the efficiency of identification and quantification of hemoglobin (Hb) Constant Spring (CS) and Hb Paksé by capillary electrophoresis (CE). Materials and methods: Blood samples collected from 2057 patients w

Externí odkaz: https://doaj.org/article/80de1ea391eb4a799b3457fb2a002b84

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Phenotypic Expression of Known and Novel Hemoglobin A2-Variants, Hemoglobin A2-Mae Phrik [Delta 52(D3) Asp > Gly, HBD:c.158A > G], Associated with Hemoglobin E [Beta 26(B8) Glu > Lys, HBB:c.79G > A] in Thailand

Autor: Amphai Phasit, Sitthichai Panyasai, Monthon Mayoon, Niphawan Jettawan, Surada Satthakarn

Publikováno v: Genes; Volume 13; Issue 6; Pages: 959

The interactions of δ-globin variants with α- and β-thalassemia or other hemoglobinopathies cause complex thalassemic syndromes and potential diagnostic problems. Understanding the molecular basis and phenotypic expression is crucial. Four unrelat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b314b0245739738f057fc30a5906e6bd

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Association of Hb Shenyang [α26(B7)Ala→Glu, GCG>GAG, HBA2: c.80C>A (or HBA1)] with Several Types of α-Thalassemia in Thailand

Autor: Sitthichai Panyasai, Kanyakan Kongthai, Amphai Phasit

Publikováno v: Hemoglobin. 44:354-360

Hb Shenyang [α26(B7)Ala→Glu, HBA2: c.80C>A (or HBA1)] is a rare α chain variant. Its genotype-phenotype relationship and origin have not been described in Thailand before. Three Thai subjects (P1–P...

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::79c915eca1996111a357acd0267d5ce3
https://doi.org/10.1080/03630269.2020.1828096

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α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [– –SEA (Southeast Asian)] Deletion in Thailand

Autor: Amphai Phasit, Sitthichai Panyasai

Publikováno v: Hemoglobin. 44:264-271

The clinical consequences of many abnormal hemoglobins (Hbs) interacting with α- or β-thalassemia (α- or β-thal) or other hemoglobinopathies have not been described. We evaluated a 75-year-old Thai woman and her 45-year-old daughter. Hematologica

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::24bcb418afa85cf4ac3c905b69e9f3a6
https://doi.org/10.1080/03630269.2020.1797773

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