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Azlin Ithnin
Azlin Ithnin
Lecturer and Head of Haematology Unit, University Kebangsaan Malaysia
Verified email at ppukm.ukm.edu.my
Title
Cited by
Cited by
Year
Glucose-6-phosphate dehydrogenase deficiency and neonatal hyperbilirubinemia: insights on pathophysiology, diagnosis, and gene variants in disease heterogeneity
HY Lee, A Ithnin, RZ Azma, A Othman, A Salvador, FC Cheah
Frontiers in pediatrics 10, 875877, 2022
902022
CD64 and group II secretory phospholipase A2 (sPLA2-IIA) as biomarkers for distinguishing adult sepsis and bacterial infections in the emergency department
TL Tan, NS Ahmad, DN Nasuruddin, A Ithnin, K Tajul Arifin, IZ Zaini, ...
PloS one 11 (3), e0152065, 2016
442016
Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM Medical Centre
RZ Azma, O Ainoon, A Hafiza, I Azlin, AR Noor Farisah, S Nor Hidayati, ...
Malays J Pathol 36 (1), 27-32, 2014
392014
Immature reticulocyte fraction is an early predictor of bone marrow recovery post chemotherapy in patients with acute leukemia
RZ Raja-Sabudin, A Othman, KA Ahmed-Mohamed, A Ithnin, H Alauddin, ...
Saudi Med J 35 (4), 346-9, 2014
262014
HbA2 levels in normal,-thalassaemia and haemoglobin E carriers by capillary electrophoresis
H Alauddin, MM Yusoff, RDA Khirotdin, A Ithnin, RZ Azma, MCK Thong, ...
Malays. j. pathol, 161-164, 2012
262012
Increased basal oxidation of peroxiredoxin 2 and limited peroxiredoxin recycling in glucose‐6‐phosphate dehydrogenase‐deficient erythrocytes from newborn infants
FC Cheah, AV Peskin, FL Wong, A Ithnin, A Othman, CC Winterbourn
The FASEB Journal 28 (7), 3205-3210, 2014
242014
Prevalence of iron deficiency anaemia and thalassaemia trait among undergraduate medical students
A Ithnin, RZ Azma
La Clinica terapeutica, 2012
242012
A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] With Other α-Thalassemias …
H Alauddin, NA Jaapar, RZ Azma, A Ithnin, NFA Razak, CK Loh, H Alias, ...
Hemoglobin 38 (4), 277-281, 2014
212014
Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice
I Azlin, FL Wong, M Ezham, A Hafiza, O Ainoon
Malays J Pathol 33 (2), 95-100, 2011
202011
Population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review
MAH Zailani, RZA Raja Sabudin, A Ithnin, H Alauddin, SA Sulaiman, ...
Frontiers in Genetics 14, 1098828, 2023
182023
Evaluation of glucose-6-phosphate dehydrogenase stability in stored blood samples
N Jalil, RZ Azma, E Mohamed, A Ithnin, H Alauddin, SN Baya, A Othman
EXCLI journal 15, 155, 2016
152016
Co-inheritance of compound heterozygous Hb Constant Spring and a single --α3.7 gene deletion with heterozygous δβ thalassaemia: A diagnostic challenge.
RZ Azma, A Othman, N Azman, H Alauddin, A Ithnin, N Yusof, NF Razak, ...
Malaysian Journal of Pathology 34 (1), 2012
152012
Genetic modifiers of fetal haemoglobin (HbF) and phenotypic severity in β-thalassemia patients
SAA Razak, NAA Murad, F Masra, DLS Chong, N Abdullah, N Jalil, ...
Current Molecular Medicine 18 (5), 295-305, 2018
122018
Glucose‐6‐phosphate dehydrogenase (G6PD)‐deficient infants: enzyme activity and gene variants as risk factors for phototherapy in the first week of life
FL Wong, A Ithnin, A Othman, FC Cheah
Journal of Paediatrics and Child Health 53 (7), 705-710, 2017
112017
Detection of α-thalassaemia in neonates on cord blood and dried blood spot samples by capillary electrophoresis
MP Hafiza Alauddin MBBS, MP Mustafa Langa MBBS, ...
The Malaysian journal of pathology 39 (1), 17, 2017
102017
Comparison of sPLA2IIA performance with high-sensitive CRP neutrophil percentage PCT and lactate to identify bacterial infection
TL Tan, CW Kang, KS Ooi, ST Tan, NS Ahmad, DN Nasuruddin, A Ithnin, ...
Scientific Reports 11 (1), 11369, 2021
92021
FISH versus real-time quantitative PCR for monitoring of minimal residual disease in chronic myeloid leukaemia patients on tyrosine kinase inhibitor therapy
AM Haidary, RZ Azma, A Ithnin, H Alauddin, NR Tumian, AM Tamil, ...
The Malaysian Journal of Pathology 41 (2), 149-160, 2019
92019
Detection of Partial G6PD Deficiency using OSMMR2000-D Kit with Hb Normalization.
A RZ, NF AR
Medicine & Health (Universiti Kebangsaan Malaysia) 9 (1), 2014
92014
Microcytic to hypochromic ratio as a discriminant index of thalassaemia trait in subjects with hypochromic anaemia
WEE Shiang Yui, SSM Said, RZAR Sabudin, H Alauddin, A Ithnin
Malays J Pathol 42 (2), 195-2011, 2020
82020
Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation
MF Alina, RZ Azma, J Norunaluwar, I Azlin, AJ Darnina, FC Cheah, ...
Journal of Human Genetics 65 (3), 263-270, 2020
82020
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Articles 1–20