Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Hafiza Alauddin"'
Autor:
Nur A’tiqah Haron, Mohamad Fikeri Ishak, Muhammad Dain Yazid, Ubashini Vijakumaran, Roszita Ibrahim, Raja Zahratul Azma Raja Sabudin, Hafiza Alauddin, Nur Ayub Md Ali, Hairulfaizi Haron, Muhammad Ishamuddin Ismail, Mohd Ramzisham Abdul Rahman, Nadiah Sulaiman
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 16, p 4774 (2024)
Coronary artery bypass grafting (CABG) utilizing saphenous vein grafts (SVGs) stands as a fundamental approach to surgically treating coronary artery disease. However, the long-term success of CABG is often compromised by the development of intimal h
Externí odkaz:
https://doaj.org/article/be1ccbacf3ab4a2688e8d55b8c087e9e
Autor:
Mohamed Afiq Hidayat Zailani, Raja Zahratul Azma Raja Sabudin, Azlin Ithnin, Hafiza Alauddin, Siti Aishah Sulaiman, Endom Ismail, Ainoon Othman
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked hereditary disorder and a global public health concern that is most prevalent in malaria-endemic regions including Asia, Africa, and the Mediterranean. G6PD-deficient indi
Externí odkaz:
https://doaj.org/article/ede23874844e4c2a97711305a5be3024
Autor:
Hamidah Alias, Woon Lee Yong, Farah Azima Abdul Muttlib, Ho Wai Koo, C-Khai Loh, Sie Chong Doris Lau, Hafiza Alauddin, Raja Zahratul Azma
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-8 (2018)
Abstract Background Acquired thrombotic thrombocytopenia purpura is very rarely encountered in children. It is often misdiagnosed initially when the condition is not inherited. Case presentation We describe a 3-year-old Malay boy who presented with s
Externí odkaz:
https://doaj.org/article/4f8802107e6a49a397ebf840726b7df5
Autor:
Norunaluwar Jalil, Raja Zahratul Azma Raja Sabudin, Sy Wee, Malisa My, Azlin Ithnin, Ainoon O, Hafiza Alauddin, Qistina Wn
Publikováno v:
Medicine & Health. 15:106-118
Haemoglobin S (HbS, α2β26GluVal) is a variant haemoglobin resulted from GAGGTG mutation on codon 6 of HBB gene. HbS haemoglobinopathy is uncommon in Malaysia and mainly seen in immigrants. However, Malaysian Indians and Malays are rarely affe
Autor:
Nor Azian Abdul Murad, Hafiza Alauddin, Rahman Jamal, Nur Azurah Abdul Ghani, Noor Hamidah Hussin, Tze Sean Khoo
Publikováno v:
Stem Cell Reviews and Reports. 16:251-261
The discovery of induced pluripotent stem (iPS) cells in 2006 marked a major breakthrough in regenerative medicine, enabling reversal of terminally differentiated somatic cells into pluripotent stem cells. The embryonic stem (ES) cells-like pluripote
Autor:
CL Wong, Nor Rafeah Tumian, Mardziah M, Salwati Shuib, Noraesah M, Azlin Ithnin, Noor Farisah Ar, Hafiza Alauddin, Raja Zahratul Azma Raja Sabudin
Publikováno v:
Medicine & Health. 14:145-156
Chronic myeloid leukemia (CML) patients who have BCR-ABL T315I mutation, usually present in the advance phase of the disease with overall survival (OS) shorter than those without the mutation. This study aimed to determine the prevalence of T315I mut
Autor:
Ainoon Othman, Hafiza Alauddin, S Fadilah S. Abdul Wahid, Noor Farisah Abdul Razak, Noor Hamidah Hussin, Wui Chuen Chia, Tze Sean Khoo, Roshida Hassan, Raja Zahratul Azma Raja Sabudin
Publikováno v:
Annals of Hematology. 98:1279-1291
Short tandem repeat (STR) analysis is used in chimerism monitoring after allogeneic hematopoietic stem cell transplantation (HSCT) for patients with various hematologic malignancies. Commercial forensic STR kits often contain loci with huge differenc
Autor:
Khairina Kamarudin, Hafiza Alauddin, Azma Rz, Noor-Farisah Razak, Loh C-Khai, Norunaluwar Jalil, Danny Koh-Xuan-Rong, Azlin Ithnin, Tang Yee Loong, Endom Ismail, Ainoon Othman, Hamidah Alias, Zarina Abdul Latiff
Publikováno v:
Hemoglobin. 42:247-251
Nondeletional α-globin mutations are known to cause more serious clinical effects than deletional ones. A rare IVS-I-1 (G>A) (HBA2: c.95+1G>A) donor splice site mutation interferes with normal splicing of pre mRNA and results in activation of a cryp
Autor:
Hamidah Alias, Ainoon Othman, Syahzuwan Hassan, Azlin Ithnin, Jalil Norunaluwar, Hafiza Alauddin, Malisa Mohd Yusoff, Zarina Abdul Latiff, Azma Rz, Nor Rafeah Tumian
Publikováno v:
Hemoglobin. 43:351-351
Autor:
Nurasyikin Yusof, Raja Zahratul Azma Raja Sabudin, Nor Rafeah Tumian, Qhasmira Abu Hazir, Norunaluwar Jalil, Hafiza Alauddin
Publikováno v:
Hemoglobin. 43:358-358
Fast-moving hemoglobins (Hbs) are a group of rare Hb variants that have a higher anodal electrophoretic mobility than Hb A on alkaline gel electrophoresis. Hb J-Bangkok (HBB: c.170G>A), a member of...