Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Wan Suriana, Wan Ab Rahman"'
Autor:
Marini Ramli, Nik Fatma Fairuz Nik Mohd Hasan, Majdan Ramli, Wan Suriana Wan Ab Rahman, Mohd Nazri Hassan, Noor Haslina Mohd Noor, Shafini Mohamed Yusoff, Salfarina Iberahim, Rosnah Bahar, Zefarina Zulkafli
Publikováno v:
Oman Medical Journal, Vol 38, Iss 3, Pp e507-e507 (2023)
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 genotypes and to estimate the range for Zone 2 peak
Externí odkaz:
https://doaj.org/article/d99d5d9ebfbf477fb99b4170560ba5e5
Autor:
Gokulakannan Venkatesan, Wan Suriana Wan Ab Rahman, Wan Nazatul Shima Shahidan, Salfarina Iberahim
Publikováno v:
Frontiers in Microbiology, Vol 14 (2023)
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. In recent years, various bioma
Externí odkaz:
https://doaj.org/article/c49b1dc180d644739ddb94cd9f0e0778
Autor:
Nazihah, Mohd Nasiruddin Dhamirah1, Wan Suriana, Wan Ab Rahman2 suriana@usm.my, Arbaeyah, Hussain Faezahtul3, Azlan, Husin4, Syazwani, Saidin Nur Ilyia1, Nazri, Hassan Mohd1, Zefarina, Zulkafli1, Shafini, Mohamed Yusof1, Salfarina, Iberahim1, Haslina, Mohd Noor Noor1
Publikováno v:
Bangladesh Journal of Medical Science. Oct2023, Vol. 22 Issue 4, p937-941. 5p.
Autor:
Divashini Vijian, Wan Suriana Wan Ab Rahman, Kannan Thirumulu Ponnuraj, Zefarina Zulkafli, Rosnah Bahar, Norafiza Yasin, Syahzuwan Hassan, Ezalia Esa
Publikováno v:
Diagnostics, Vol 13, Iss 5, p 894 (2023)
(1) Background: Alpha (α)-thalassaemia is a genetic disorder that affects 5% of the world population. Deletional or nondeletional mutations of one or both HBA1 and HBA2 on chromosome 16 will result in reduced production of α-globin chains, a compon
Externí odkaz:
https://doaj.org/article/ad5c9b5808104310ad78efb95ab36be8
Autor:
Zefarina Zulkafli, Theeba Janaveloo, Wan Suriana Wan Ab Rahman, Mohd Nazri Hassan, Wan Zaidah Abdullah
Publikováno v:
Oman Medical Journal, Vol 34, Iss 4, Pp 336-340 (2019)
Thrombocytosis in children as well as in adult is defined as platelet count ≥ 450 × 109/L, and it is usually a reactive feature to various medical disorders. However, extreme thrombocytosis (platelet count ≥ 1000 × 109/L) is an uncommon finding
Externí odkaz:
https://doaj.org/article/0028f1954a904151a6375472ea22c0ce
Autor:
Siti Nur Nabeela A’ifah Mohammad, Salfarina Iberahim, Wan Suriana Wan Ab Rahman, Mohd Nazri Hassan, Hisham Atan Edinur, Maryam Azlan, Zefarina Zulkafli
Publikováno v:
Diagnostics, Vol 12, Iss 6, p 1374 (2022)
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 organs. Those afflicted with this condition may feel lethargic a
Externí odkaz:
https://doaj.org/article/61fc07b9b82443398ed94ac35ba90775
Autor:
Che Faridah Che Wanik, Mohd Nazri Hassan, Noor Haslina Mohd Noor, Marini Ramli, Salfarina Iberahim, Zefarina Zulkafli, Wan Suriana Wan Ab Rahman, Shafini Mohamed Yusoff, Rosnah Bahar
Publikováno v:
Bangladesh Journal of Medical Science. 22:379-384
Background: Alloimmunization is a known complication following repeated red blood cell transfusions. However, the associated factors of RBC alloimmunization are different among blood recipient groups. This study aimed to determine the associated fact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d60da2d1e7e1124af13b0fe2b2f9c4e
https://doi.org/10.3329/bjms.v22i2.64999
https://doi.org/10.3329/bjms.v22i2.64999
Autor:
Mohd Nazri Hassan, Noor Haslina Mohd Noor, Marini Ramli, Wan Suriana Wan Ab Rahman, Zefarina Zulkafli, Rosnah Bahar, Shafini Mohamed Yusoff, Salfarina Iberahim, Marne Abdullah
Publikováno v:
Asian Journal of Medicine and Biomedicine. 6:132-138
Clinical demand for blood transfusion is endless, and patients are exposed to the risk of transfusion error at any point along the transfusion chain which lead to incorrect blood component transfused (IBCT) if the standard transfusion practices have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28ca6942688bd1e0ae919c813cb5b5dc
https://doi.org/10.37231/ajmb.2022.6.2.484
https://doi.org/10.37231/ajmb.2022.6.2.484
Publikováno v:
Malaysian Journal of Medicine and Health Sciences. 18:190-199
Alpha (α)-thalassaemia is a common genetic disorder worldwide caused by the deletion and rarely non-deletional mutations of the α-globin gene. Nearly 70 types of non-deletional mutations have been reported worldwide, and this review focuses on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dae45d26b4a12506ea4c80f0cbb05e30
https://doi.org/10.47836/mjmhs.18.5.26
https://doi.org/10.47836/mjmhs.18.5.26
Autor:
Siti Nazihahasma Hassan, Suharni Mohamad, Rosline Hassan, Shuangshi Wei, Noor Haslina Mohd Noor, Wan Suriana Wan Ab Rahman
Publikováno v:
Bangladesh Journal of Medical Science. 21:432-437
Background:MNS glycophorin variants such as glycoprotein (GP.) Mur, GP.Hop, GP.Bun, GP.HF, GP.Hut, and GP.Vw are known to carry multiple antigens, including Mia (MNS7). In East and Southeast Asians, an antibody to Mia is not only commonly found, but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02e2889e2cc901f83390886187db88d7
https://doi.org/10.3329/bjms.v21i2.58078
https://doi.org/10.3329/bjms.v21i2.58078