Pranee Sutcharitchan
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Explore the profile of Pranee Sutcharitchan including associated specialties, affiliations and a list of published articles.
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33
Citations
258
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Recent Articles
1.
Suksusut A, Jaitheang J, Prapphal M, Sutcharitchan P, Rojnuckarin P, Uaprasert N
Hematology
. 2025 Jan;
30(1):2456679.
PMID: 39878036
Background: Hemoglobin (Hb) Hekinan is a prevalent α-globin variant frequently missed in thalassemia screening centers using high-performance liquid chromatography (HPLC) or capillary electrophoresis. This study aims to investigate the hematological...
2.
Songdej D, Teawtrakul N, Laoaroon N, Komvilaisak P, Sripornsawan P, Surapolchai P, et al.
Br J Haematol
. 2024 Oct;
206(2):703-712.
PMID: 39478290
Haemoglobin (Hb) H disease and HbH disease with co-inherited HbE mutation are the most prevalent forms of α-thalassaemia in Southeast Asia. Data were limited when comparing clinical phenotypes between these...
3.
Songdej D, Surapolchai P, Komwilaisak P, Sripornsawan P, Lauhasurayotin S, Teawtrakul N, et al.
Ann Hematol
. 2023 Dec;
103(2):395.
PMID: 38040861
No abstract available.
4.
Songdej D, Surapolchai P, Komwilaisak P, Sripornsawan P, Lauhasurayotin S, Teawtrakul N, et al.
Ann Hematol
. 2023 Nov;
103(2):385-393.
PMID: 37996759
Red blood cell (RBC) membrane disorders represent a significant category of hereditary hemolytic anemia; however, information from Southeast Asia is limited. We established a national registry aiming to characterize RBC...
5.
Thavonlun S, Houngngam N, Kingpetch K, Numkarunarunrote N, Santisitthanon P, Buranasupkajorn P, et al.
Sci Rep
. 2023 Sep;
13(1):16413.
PMID: 37775530
Patients with transfusion-dependent thalassemia (TDT) have an increased risk of osteoporosis and fractures. They also have several potential factors associated with sarcopenia. There has been currently no study on sarcopenia...
6.
Surapolchai P, Songdej D, Hantaweepant C, Tantiworawit A, Charoenkwan P, Lauhasurayotin S, et al.
Pediatr Blood Cancer
. 2023 Jul;
70(10):e30599.
PMID: 37488065
Introduction: Management of transfusion-dependent thalassemia (TDT) can be challenging due to numerous potential disease-related complications and comorbidities in particular age groups. The objective of this study was to report thalassemia-related...
7.
Deferiprone, an iron chelator, alleviates platelet hyperactivity in patients with β-thalassaemia/HbE
Tran N, Sutcharitchan P, Janprasit J, Rojnuckarin P, Morales N, Luechapudiporn R
Drugs Context
. 2022 Dec;
11.
PMID: 36544626
Background: Hyperfunctional platelets play important roles in thromboembolism in patients with β-thalassaemia/ haemoglobin E (β-thal/HbE). Our previous study revealed ex vivo inhibitory effects of deferiprone on normal platelets. Herein, we...
8.
Jaitheang J, Suksusut A, Settapiboon R, Amornsiriwat S, Sutcharitchan P, Uaprasert N, et al.
Lab Med
. 2022 Oct;
54(3):e91-e94.
PMID: 36282478
Objective: Hemoglobin Constant Spring (HbCS) is often missed by routine hemoglobin analysis. The aim of this research was to study HbCS stability as identified by capillary electrophoresis (CE) to determine...
9.
Teawtrakul N, Songdej D, Hantaweepant C, Tantiworawit A, Lauhasurayotin S, Torcharus K, et al.
Transfusion
. 2022 Aug;
62(10):2039-2047.
PMID: 35986658
Background: Thalassemia is a common genetic disease in Southeast Asia. Red blood cell (RBC) transfusion is an essential treatment for severe forms of thalassemia. We performed a study to demonstrate...
10.
Cappellini M, Kattamis A, Viprakasit V, Sutcharitchan P, Pariseau J, Laadem A, et al.
Am J Hematol
. 2019 Jul;
94(10):E261-E264.
PMID: 31321793
No abstract available.