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Wan Suriana Wan Ab Rahman

Explore the profile of Wan Suriana Wan Ab Rahman including associated specialties, affiliations and a list of published articles. Areas
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Articles 15
Citations 24
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Recent Articles
1.
Kochuthakidiyel Suresh P, Sekar G, Mallady K, Wan Ab Rahman W, Shima Shahidan W, Venkatesan G
JMIR Bioinform Biotechnol . 2024 Jun; 4:e37306. PMID: 38935956
Background: Dengue fever can progress to dengue hemorrhagic fever (DHF), a more serious and occasionally fatal form of the disease. Indicators of serious disease arise about the time the fever...
2.
Iberahim S, Muhamat Yusoff R, Noor N, Hassan R, Ramli N, Bahar R, et al.
Cureus . 2024 Feb; 16(1):e51483. PMID: 38304638
Background Prolonged immobilization is widely recognized as a risk factor for thromboembolism. In this prospective study, we investigated the changes in clot waveform analysis (CWA) parameters in prolonged immobilized patients...
3.
Hassan S, Mohamad S, Kannan T, Hassan R, Wei S, Wan Ab Rahman W
Asian J Transfus Sci . 2024 Jan; 17(2):169-174. PMID: 38274953
Background And Objective: A number of glycophorin variant phenotypes or hybrid glycophorin variants of the MNS blood group system bear multiple immunogenic antigens such as Mi, Mur, and MUT. In...
4.
Mohd Shukri N, Wan Mohamad W, Wan Ab Rahman W
Cureus . 2023 Nov; 15(11):e49205. PMID: 38024034
Childhood-onset systemic lupus erythematosus is a rare disease that is more prevalent in Southeast Asian children than in Western children. It is characterised by a peripubertal onset and a female...
5.
Ramli M, Nik Mohd Hasan N, Ramli M, Wan Ab Rahman W, Hassan M, Noor N, et al.
Oman Med J . 2023 Jun; 38(3):e507. PMID: 37351377
Objectives: Hemoglobin constant spring (Hb CS) is a point mutational defect associated with α thalassemia. The aims of this study were to compare the hematological profiles between different Hb CS...
6.
Habib Dzulkarnain S, Hashim I, Zainudeen Z, Taib F, Mohamad N, Nasir A, et al.
J Clin Immunol . 2023 Jun; 43(7):1623-1639. PMID: 37328647
Purine nucleoside phosphorylase deficient severe combined immunodeficiency (PNP SCID) is one of the rare autosomal recessive primary immunodeficiency disease, and the data on epidemiology and outcome are limited. We report...
7.
Venkatesan G, Wan Ab Rahman W, Shima Shahidan W, Iberahim S, Muhd Besari Hashim A
Front Microbiol . 2023 May; 14:1097173. PMID: 37125151
Early disease diagnosis is critical for better management and treatment outcome of patients. Therefore, diagnostic methods should ideally be accurate, consistent, easy to perform at low cost and preferably non-invasive....
8.
Vijian D, Wan Ab Rahman W, Ponnuraj K, Zulkafli Z, Bahar R, Yasin N, et al.
Diagnostics (Basel) . 2023 Mar; 13(5). PMID: 36900038
(1) Background: Alpha (α)-thalassaemia is a genetic disorder that affects 5% of the world population. Deletional or nondeletional mutations of one or both and on chromosome 16 will result in...
9.
Zulkeflee R, Hassan M, Hassan R, Saidin N, Zulkafli Z, Ramli M, et al.
Transfus Apher Sci . 2023 Feb; 62(3):103658. PMID: 36805153
Acute hemolytic transfusion reaction following ABO-incompatible platelet transfusion: two case reports An ideal platelet transfusion should provide ABO identical platelet concentrate, and cross match compatibility is not routinely performed in...
10.
Mohammad S, Iberahim S, Wan Ab Rahman W, Hassan M, Edinur H, Azlan M, et al.
Diagnostics (Basel) . 2022 Jun; 12(6). PMID: 35741184
Anemia is a condition in which red blood cells and/or hemoglobin (Hb) concentrations are decreased below the normal range, resulting in a lack of oxygen being transported to tissues and...