Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Rosnah Bahar"'
Autor:
Rosnah Bahar, Vasuhi Kalimuthu, Muhammad Farid Johan, Siti Zubaidah Mustapha, Zefarina Zulkafli
Publikováno v:
Liaquat National Journal of Primary Care, Vol 6, Iss 3, Pp 232-239 (2024)
Background: To date, more than 70 variants of non-deletional mutations associated with α-thalassaemia have been recognized and recorded, showcasing the diverse genetic manifestations of the condition. Objective: This study is to provide data on th
Externí odkaz:
https://doaj.org/article/27c141626c3a46919d0d28d5fed63840
Autor:
Sarah Abdul Halim, Rosnah Bahar, Wan Zaidah Abdullah, Erinna Mohamad Zon, Shafini Mohamed Yusoff
Publikováno v:
Oman Medical Journal, Vol 38, Iss 4, Pp e524-e524 (2023)
Objectives: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymopathy worldwide. The fluorescent spot test (FST) is the conventional method for screening neonates for G6PD. However, it has limitations and quantitative assays
Externí odkaz:
https://doaj.org/article/96c975c4543c476a922c2f6a661df67c
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:
Salfarina Iberahim, Noor Haslina Mohd Noor, Mohd Nazri Hassan, Rosnah Bahar, Shafini Mohdmed Yusoff, Marini Ramli, Wan Suriana Wan Abdul Rahman, Zefarina Zulkafli, Marne Abdullah, Ho Sook Fong, Tengku Muzaffar Tengku Mohamed Shihabudin, Hisham Atan Edinur, Norul Hajar Che Ghazali
Publikováno v:
Asian Journal of Transfusion Science, Vol 16, Iss 2, Pp 276-279 (2022)
The Diego (Di) blood group system comprises 22 antigens located on the band 3 protein, most of which are low-prevalence antigens. The majority of antibodies to Diego system antigens were of clinically insignificant; however anti-Dia, -Dib, -Wra, -ELO
Externí odkaz:
https://doaj.org/article/1a48b57f90a941ae9ac52923c9ea758f
Autor:
Wan Nor Fazila Hafizan Wan Nik, Noorazliyana Shafii, Noor Azlin Azraini Che Soh1 and, Rosnah Bahar
Publikováno v:
Oman Medical Journal, Vol 37, Iss 4, Pp e393-e393 (2022)
Glycated hemoglobin (HbA1c) is used to monitor the long-term management of diabetes and reflects the average blood glucose level over the past three months. Hb J is an alpha-globin gene variant that occurs less commonly but can interfere with the HbA
Externí odkaz:
https://doaj.org/article/8734cbf2d4454698b4531c2824019ec5
Autor:
Nur Atikah Zakaria, Rosnah Bahar, Wan Zaidah Abdullah, Abdul Aziz Mohamed Yusoff, Shaharum Shamsuddin, Ridhwan Abdul Wahab, Muhammad Farid Johan
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Thalassemias are monogenic hematologic diseases that are classified as α- or β-thalassemia according to its quantitative abnormalities of adult α- or β-globin chains. β-thalassemia has widely spread throughout the world especially in Mediterrane
Externí odkaz:
https://doaj.org/article/4abf11e7cb924a9cbb0f7c3358ee8115
Autor:
Razan Hayati Zulkeflee, Rosnah Bahar, Marne Abdullah, Muhammad Amiro Rasheeq Mohd Radzi, Alina Md Fauzi, Rosline Hassan
Publikováno v:
Diagnostics, Vol 13, Iss 8, p 1379 (2023)
Thalassemia is identified as a prevalent disease in Malaysia, known to be one of the developing countries. Fourteen patients with confirmed cases of thalassemia were recruited from the Hematology Laboratory. The molecular genotypes of these patients
Externí odkaz:
https://doaj.org/article/24ac5acfb10a4928ba00b1a9760015de
Autor:
Zefarina Zulkafli, Mohd Nazri Hassan, Shafini Mohd Yusoff, Noor Haslina Mohd Noor, Suryati Hussin, Nor Khairina Mohamed Kamarudin, Yuslina Mat Yusoff, Rosnah Bahar
Publikováno v:
Oman Medical Journal, Vol 37, Iss 1, Pp e331-e331 (2022)
Patients with heterozygous β-thalassemia are generally asymptomatic. However, the intermediate phenotype is uncommon, and patients require further investigation to confirm the diagnosis. We describe a 32-year-old woman (gravida 3, para 2) with heter
Externí odkaz:
https://doaj.org/article/d20ed595cca344018ad4f5286732155e
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:
Syahzuwan Hassan, Rosnah Bahar, Muhammad Farid Johan, Ezzeddin Kamil Mohamed Hashim, Wan Zaidah Abdullah, Ezalia Esa, Faidatul Syazlin Abdul Hamid, Zefarina Zulkafli
Publikováno v:
Diagnostics, Vol 13, Iss 3, p 373 (2023)
Thalassemia is one of the most heterogeneous diseases, with more than a thousand mutation types recorded worldwide. Molecular diagnosis of thalassemia by conventional PCR-based DNA analysis is time- and resource-consuming owing to the phenotype varia
Externí odkaz:
https://doaj.org/article/15a4501740da4bf7b2782277d15d0e65