Pranee Winichagoon
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Explore the profile of Pranee Winichagoon including associated specialties, affiliations and a list of published articles.
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Citations
499
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Recent Articles
1.
Chaichompoo P, Nithipongvanitch R, Kheansaard W, Tubsuwan A, Srinoun K, Vadolas J, et al.
Sci Rep
. 2022 Nov;
12(1):18628.
PMID: 36329049
β-Thalassaemia results from defects in β-globin chain production, leading to ineffective erythropoiesis and subsequently to severe anaemia and other complications. Apoptosis and autophagy are the main pathways that regulate the...
2.
Paiboonsukwong K, Jopang Y, Winichagoon P, Fucharoen S
Hemoglobin
. 2022 Aug;
46(1):53-57.
PMID: 35950590
Thailand has a population of 66.2 million with 30.0-40.0% of them carrying thalassemia genes. Interaction of these thalassemia genes lead to more than 60 genotypes with a wide spectrum of...
3.
Suriyun T, Winichagoon P, Fucharoen S, Sripichai O
J Clin Med
. 2022 Apr;
11(7).
PMID: 35407362
Anemia in β-thalassemia is associated with ineffective erythropoiesis and a shortened lifespan of erythroid cells. The limited differentiation of β-thalassemic erythroblasts has been documented, but the characteristic feature of terminal...
4.
Munkongdee T, Nualkaew T, Buasuwan N, Hinna N, Paiboonsukwong K, Sripichai O, et al.
Int J Lab Hematol
. 2020 Jul;
42(6):727-733.
PMID: 32706939
Introduction: Several DNA-based approaches including a reverse dot-blot hybridization (RDB) have been established for detection of β-thalassemia genotypes to provide accurate genetic counseling and prenatal diagnosis for prevention and control...
5.
Munkongdee T, Chen P, Winichagoon P, Fucharoen S, Paiboonsukwong K
Front Mol Biosci
. 2020 Jul;
7:74.
PMID: 32671092
Alpha- and β-thalassemias and abnormal hemoglobin (Hb) are common in tropical countries. These abnormal globin genes in different combinations lead to many thalassemic diseases including three severe thalassemia diseases, i.e.,...
6.
Jintaridth P, Srisomsap C, Vichittumaros K, Kalpravidh R, Winichagoon P, Fucharoen S, et al.
Int J Hematol
. 2018 Jan;
83(5):408-414.
PMID: 29349701
Immunoglobulin Y (IgY) technology was used to generate anti-hemoglobin Bart's (Hb Bart's) IgY antibodies (Abs) for development into an enzyme-linked immunosorbent assay (ELISA) test for thalassemia diagnosis. Hb Bart's purified...
7.
Siwaponanan P, Fucharoen S, Sirankapracha P, Winichagoon P, Umemura T, Svasti S
Int J Hematol
. 2016 Jun;
104(3):338-43.
PMID: 27272941
Ineffective erythropoiesis in β-thalassemia patients is caused by the premature death of red blood cell precursors due to excess α-globin chains. As a consequence, patients develop chronic anemia and hypoxia....
8.
Munkongdee T, Tanakulmas J, Butthep P, Winichagoon P, Main B, Yiannakis M, et al.
Hemoglobin
. 2016 Apr;
40(3):163-7.
PMID: 27117566
Determining the magnitude of the thalassemia problem in a country is important for implementing a national prevention and control program. In order to acquire accurate thalassemia prevalence data, the gene...
9.
Winichagoon P, Kumbunlue R, Sirankapracha P, Boonmongkol P, Fucharoen S
Blood Cells Mol Dis
. 2015 Jan;
54(4):336-41.
PMID: 25633854
Decreased hemoglobinization of red cells resulting in hypochromia and microcytosis are the main features of thalassemia syndromes, and also of iron deficiency anemia (IDA). A simple and reliable method is...
10.
Chaichompoo P, Pattanapanyasat K, Winichagoon P, Fucharoen S, Svasti S
Blood Cells Mol Dis
. 2015 Jan;
55(2):173-9.
PMID: 25631622
β-Thalassemia/HbE disease is caused by a defective β-globin synthesis that leads to accumulation of excess unbound α-globins, and consequently oxidative stress, ineffective erythropoiesis and chronic anemia. Cell replication and oxidative...