Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Sitthichai Panyasai"'
Publikováno v:
Libyan Journal of Medicine, Vol 19, Iss 1 (2024)
To determine the molecular basis, genotype – phenotype relationship, and genetic origin of Hemoglobin (Hb) Hekinan associated with several forms of α-thalassemia and other hemoglobinopathies for a better understanding of its diverse clinical pheno
Externí odkaz:
https://doaj.org/article/c1e3f8f63edf4f10aeda1528b760696b
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 16, p 8578 (2024)
Hemoglobin Shaare Zedek (Hb SZ) is a rare structural α-Hb variant. Characterizing its genotype–phenotype relationship and genetic origin enhances diagnostic and clinical management insights. We studied a proband and six family members using high-p
Externí odkaz:
https://doaj.org/article/a8cdab5ae92442eb9221daffc71b61a3
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract α-thalassemia is an inherited blood disorder that is most frequently found in Southeast Asian populations. In Thailand, molecular characterization can diagnose most patients with α-thalassemia; however, several atypical patients are also o
Externí odkaz:
https://doaj.org/article/448416539ab94f028f87d0d713a4cb4e
Publikováno v:
Annals of Medicine, Vol 55, Iss 2 (2023)
AbstractBackground Low HbF expression in HbE-β+-thalassemia may lead to misdiagnosis of HbE heterozygosity. We aimed to characterize the β- and α-globin genes and the modifying factors related to HbF expression in patients with an Hb phenotype sim
Externí odkaz:
https://doaj.org/article/bb8a87cf2fcb4700be98a88e721ea02d
Publikováno v:
Annals of Medicine, Vol 55, Iss 2 (2023)
AbstractBackground An increasing number of α-hemoglobin (Hb) variants is causing various clinical symptoms; therefore, accurate identification of these Hb variants is important.Objective This study aimed to describe the molecular and hematological c
Externí odkaz:
https://doaj.org/article/85c3e19553d64ea4bbea3ee0f2832066
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
Autor:
Sarayot Rareongjai, Sitthichai Panyasai, Santipap Sooncharoen, Soraya Mol-ar, Orathai Pongtussanahem
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 37, Iss 1, Pp 25-34 (2019)
Objective: To evaluate the efficiencies of the standard α thalassemia screening regimen in human immunodeficiency virus (HIV) infected patients and improve the efficiencies of this screening regimen using new cutoff values. Material and Methods: A s
Externí odkaz:
https://doaj.org/article/5221bde4d8ed47dda762ea55808b354a
Publikováno v:
Asian Journal of Transfusion Science, Vol 11, Iss 2, Pp 199-202 (2017)
Hemoglobin (Hb) D-Punjab [β 121(GH4) Glu→ln; HBB: C.364G>C] and β0-thalassemia 3.4 kb deletion are very rare in the Thai population. For the first time, the coinheritance of HbD-Punjab with β0-thalassemia 3.4 kb deletion was reported in a 7-year
Externí odkaz:
https://doaj.org/article/3629c87b85f146f6a6aa9a5c653b01b7
Autor:
Sitthichai Panyasai
Publikováno v:
Journal of Associated Medical Sciences, Vol 45, Iss 1, Pp 49-49 (2012)
There are high prevalence of β-thalassemia and α-thalassemia in the upper Northern Thailand. Thus, the interaction between β-thalassemia and α-thalassemia can be occurred. The aim of this study was to analyze the incidence of gene interaction bet
Externí odkaz:
https://doaj.org/article/f26dcd6cf9014e2baabff2ae884b237f
Publikováno v:
Journal of Associated Medical Sciences, Vol 41, Iss 2, Pp 94-94 (2008)
At present, one-tube osmotic fragility test (OFT) is used to screen severe thalassemia carriers. This study was aimed to study of stability of blood used in the osmotic fragility test (OFT). One hundred and fourteen EDTA blood samples were recruited,
Externí odkaz:
https://doaj.org/article/8a3fbecc155f44f387bd721309fd77e8