Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Rossarin Karnpean"'
Autor:
Rossarin Karnpean, Nawinda Vanichakulthada, Wanwisa Suwannaloet, Ruttiya Thongrung, Sanita Singsanan, Nattapol Prakobkaew, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Anemia is a major public health problem in many areas of Southeast Asia. Ascertaining anemia and defining its underlying causes is essential for providing appropriate care, management, and establishment of a control program. Limited studies
Externí odkaz:
https://doaj.org/article/0fec3cab22554e5d859e1d0ed63da5aa
Autor:
Sanita Singsanan, Supawadee Yamsri, Kanjana Pangjit, Phairo Saenwang, Rossarin Karnpean, Supan Fucharoen
Publikováno v:
Genetic testing and molecular biomarkers. 26(6)
Autor:
Rossarin Karnpean, Wanicha Tepakhan, Prame Suankul, Sitthikorn Thingphom, Apichaya Poonsawat, Naritthakarn Thanunchaikunlanun, Rotsakorn Ruangsanngamsiri, Wittaya Jomoui
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1384
Single nucleotide polymorphisms are informative for haplotype analysis associated with genetic background and clinical linkage studies of β-thalassemia mutations. Hence, the aim of this study was to investigate five polymorphisms (codon 2 (C/T), IVS
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
Autor:
Preawwalee Wintachai, Thanyaornwanya Charoenwijitkul, Phuthita Thepphitak, Kritsada Singha, Rossarin Karnpean, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Supan Fucharoen
Publikováno v:
Clinical Biochemistry. 71:31-37
Objective The 3.7 kb deletion (-α 3.7 ) is the most common form of α + -thalassemia found in multiple populations which can be classified into three subtypes. In order not to mis-identify it, the molecular information within each population is requ
Autor:
Roongnalin Bunthupanich, Nawinda Jiambunsri, Anuwat Pinyachat, Rossarin Karnpean, Nattapol Prakobkaew, Supan Fucharoen, Suthat Fucharoen, Naruwat Pakdee
Publikováno v:
Hemoglobin. 44(3)
Northeastern (NE) Thailand is one of the areas with a prevalence of thalassemias and hemoglobinopathies. Data on the prevalence of the diseases in minorities in the region has been limited. This study aimed to survey the thalassemias and hemoglobinop
Publikováno v:
Journal of clinical pathology. 73(8)
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
Publikováno v:
Hemoglobin. 43(4-5)
The α
Autor:
Duangrudee Changtrakul, Goonnapa Fucharoen, Anupong Pansuwan, Rossarin Karnpean, Supan Fucharoen
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 51:1265-1271
Background: No external quality assessment program for hemoglobin (Hb) analysis in the prevention and control of thalassemia has been established in Thailand. To improve the first line provisional diagnostics, the first proficiency testing (PT) progr
Publikováno v:
Clinical Biochemistry. 44:889-893
Background The effectiveness of the URIT-2900 Hematology Analyzer for screening of hemoglobinopathies commonly found in Southeast Asian populations was examined. Methods Appropriate cut-off values of MCV and MCH for screening of α 0 and β thalassem