Suthat Fucharoen
Overview
Explore the profile of Suthat Fucharoen including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
261
Citations
3313
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Piriyapongsa J, Chumnumwat S, Kaewprommal P, Triparn K, Suvichapanich S, Udomsinprasert W, et al.
Sci Rep
. 2024 Dec;
14(1):30683.
PMID: 39730427
Inter-individual variability in drug responses is significantly influenced by genetic factors, underscoring the importance of population-specific pharmacogenomic studies to optimize clinical outcomes. In this study, we analyzed whole genome sequencing...
2.
Nonejuie P, Wilantho A, McDonald D, Htoo H, Chalerm J, Tripathi A, et al.
Sci Rep
. 2024 Oct;
14(1):23858.
PMID: 39394230
Recent research highlights the significant impact of the gut microbiota on health and disease. Thalassemia, a hereditary blood disorder, requires regular blood transfusions, leading to an accumulation of iron in...
3.
Fianza P, Pramono A, Ghozali M, Sihite T, Setiabudi D, Syamsunarno M, et al.
Rev Cardiovasc Med
. 2024 Jul;
23(8):267.
PMID: 39076648
Thalassemia major is the most common monogenetic disorder worldwide, manifested as chronic hemolytic anemia. This condition leads to the need for chronic blood transfusion to be monitored for an iron...
4.
Tong-Ngam P, Wongkummool W, Pongpaksupasin P, Rawara N, Kovanich D, Kitiyanant N, et al.
Stem Cell Res
. 2023 Oct;
73:103228.
PMID: 37890329
Hemoglobin E (HbE), a common variant in Southeast Asian populations, results from a G to A substitution at codon 26 of the HBB gene, causing abnormal Hb and mild β-thalassemia-like...
5.
Limwongse C, Rojnuckarin P, Kupatawintu P, Thongthaisin A, Permpikul P, Kitpoka P, et al.
Transfus Med
. 2023 Sep;
33(6):497-502.
PMID: 37775960
Background And Objective: The mainstay of management for thalassemia is regular blood transfusions. However, gaps and unmet needs of blood services for thalassemia are still not clearly identified and addressed...
6.
Chumchuen S, Sripichai O, Jearawiriyapaisarn N, Fucharoen S, Peerapittayamongkol C
PLoS One
. 2023 Mar;
18(3):e0281059.
PMID: 36888630
Imbalanced globin chain output contributes to thalassemia pathophysiology. Hence, induction of fetal hemoglobin in β-thalassemia and other β-hemoglobinopathies are of continuing interest for therapeutic approaches. Genome-wide association studies have identified...
7.
Sripetchwandee J, Khamseekaew J, Svasti S, Srichairatanakool S, Fucharoen S, Chattipakorn N, et al.
Life Sci
. 2023 Jan;
315:121401.
PMID: 36681579
No abstract available.
8.
Settakorn K, Kongkarnka S, Chompupoung A, Svasti S, Fucharoen S, Porter J, et al.
Front Physiol
. 2023 Jan;
13:1053060.
PMID: 36620219
β-Thalassemia is characterized by ineffective erythropoiesis leading to chronic anemia. Thus, increased iron absorption from the duodenum and via blood transfusions is required to maintain normal blood hemoglobin (Hb) levels...
9.
Wongkummool W, Tong-Ngam P, Munkongdee T, Tangprasittipap A, Paiboonsukwong K, Hongeng S, et al.
Stem Cell Res
. 2022 Nov;
65:102979.
PMID: 36427475
Hemoglobin Constant Spring (HbCS) is unstable hemoglobin resulting from a nucleotide substitution at the termination codon of the HBA2 gene (c.427 T > C). The homozygous state for HbCS is...
10.
Pimpakan T, Mungkalasut P, Tansakul P, Chanda M, Jugnam-Ang W, Charucharana S, et al.
BMC Pediatr
. 2022 Nov;
22(1):678.
PMID: 36419023
Background: Screening for G6PD deficiency in newborns can help prevent severe hemolysis, hyperbilirubinemia, and bilirubin encephalopathy, as recommended by the World Health Organization (WHO). It has been speculated that the...