Zobrazeno 1 - 5
of 5
pro vyhledávání: '"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
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
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...
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
Autor:
Sitthichai, Panyasai, Amphai, Phasit
Publikováno v:
Hemoglobin. 44(4)
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