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Prevalence and molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Senoi Malaysian Orang Asli population

PloS one, 2023-12, Vol.18 (12), p.e0294891-e0294891

2023

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Population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review

Frontiers in genetics, 2023-06, Vol.14, p.1098828-1098828

2023

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Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity

Frontiers in pediatrics, 2022-05, Vol.10, p.875877-875877

2022

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Increased basal oxidation of peroxiredoxin 2 and limited peroxiredoxin recycling in glucose‐6‐phosphate dehydrogenase‐deficient erythrocytes from newborn infants

The FASEB journal, 2014-07, Vol.28 (7), p.3205-3210

2014

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Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia

Pediatrics international, 2009-08, Vol.51 (4), p.488-493

2009

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Prevalence and molecular heterogeneity of glucose-6-phosphate dehydrogenase

PloS one, 2023-12, Vol.18 (12), p.e0294891

2023

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The incorporation of the Halal Management System (HMS) by the pharmaceutical industry

GaBI Journal, 2023-09, Vol.12 (3), p.1

2023

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Molecular Characterisation of α‐ and β‐Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia

Annals of human genetics, 2017-09, Vol.81 (5), p.205-212

2017

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The incorporation of the Halal Management System (HMS) by the pharmaceutical industry

GaBI Journal, 2023-01, Vol.12 (3), p.87-94

2023

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Siriraj I G (A δβ)0-thalassaemia causing severe thalassaemia intermedia in compound heterozygous state with IVS1-1(G-T) mutation

Malaysian journal of pathology, 2021-04, Vol.43 (1), p.95-100

2021

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Updates on Laboratory Tests for Diagnosis of Glucose-6-Phosphate Dehydrogenase Deficiency in Malaysia

Hemoglobin, 2019-11, Vol.43 (6), p.312-312

2019

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HPLC Tosoh HLC-723 G8 Analyzer Performance in Detection of β-Thalassemia and Hb E Traits

Hemoglobin, 2019-11, Vol.43 (6), p.355-355

2019

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Application of Molecular Diagnostics in Detection of β-Thalassemia and Hemoglobin Variants at Hospital Canselor Tuanku Muhriz UKM, Kuala Lumpur, Malaysia

Hemoglobin, 2019-11, Vol.43 (6), p.351-351

2019

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Glucose‐6‐phosphate dehydrogenase (G6PD)‐deficient infants: Enzyme activity and gene variants as risk factors for phototherapy in the first week of life

Journal of paediatrics and child health, 2017-07, Vol.53 (7), p.705-710

2017

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Evaluation of quantitative point-of-care test for measurement of glucose-6-phosphate dehydrogenase enzyme activity in Malaysia

Malaysian journal of pathology, 2023-04, Vol.45 (1), p.31-41

2023

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Molecular Characterisation of [alpha]- and [beta]-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia

Annals of human genetics, 2017-09, Vol.81 (5), p.205

2017

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Team-Based Learning: Benefits on Learning and Students’ Perception

Education in medicine journal, 2019-12, Vol.14 (4), p.61-69

2019

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Multiplex STR panel for assessment of chimerism following hematopoietic stem cell transplantation (HSCT)

Annals of hematology, 2019-05, Vol.98 (5), p.1279-1291

2019

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Importance of extended blood group genotyping in multiply transfused patients

Transfusion and apheresis science, 2017-06, Vol.56 (3), p.410-416

2017

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Evaluation of Glucose-6-Phosphate Dehydrogenase stability in stored blood samples

EXCLI journal, 2016-01, Vol.15, p.155-162

2016

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A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia

Hemoglobin, 2018-07, Vol.42 (4), p.247-251

2018

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Risk Factors Associated with Unconjugated Neonatal Hyperbilirubinemia in Malaysian Neonates

Journal of tropical pediatrics (1980), 2013-08, Vol.59 (4), p.280-285

2013

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Phoenix dactylifera (date fruits) administration to animal models of neurological diseases: A systematic review of health benefits

Current topics in nutraceuticals research, 2016-08, Vol.14 (3), p.181

2016

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Ex vivo expanded SSEA-4+ human limbal stromal cells are multipotent and do not express other embryonic stem cell markers

Molecular vision, 2012-05, Vol.18, p.1289-1300

2012

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Hemoglobinopathies and thalassemia screening among Senoi Orang Asli in Peninsular Malaysia

AIP Conference Proceedings, 2015, Vol.1678 (1)

2015

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Prevalence and molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Senoi Malaysian Orang Asli population

Population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review

Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity

Increased basal oxidation of peroxiredoxin 2 and limited peroxiredoxin recycling in glucose‐6‐phosphate dehydrogenase‐deficient erythrocytes from newborn infants

Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia

Prevalence and molecular heterogeneity of glucose-6-phosphate dehydrogenase

The incorporation of the Halal Management System (HMS) by the pharmaceutical industry

Molecular Characterisation of α‐ and β‐Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia

The incorporation of the Halal Management System (HMS) by the pharmaceutical industry

Siriraj I G (A δβ)0-thalassaemia causing severe thalassaemia intermedia in compound heterozygous state with IVS1-1(G-T) mutation

Updates on Laboratory Tests for Diagnosis of Glucose-6-Phosphate Dehydrogenase Deficiency in Malaysia

HPLC Tosoh HLC-723 G8 Analyzer Performance in Detection of β-Thalassemia and Hb E Traits

Application of Molecular Diagnostics in Detection of β-Thalassemia and Hemoglobin Variants at Hospital Canselor Tuanku Muhriz UKM, Kuala Lumpur, Malaysia

Glucose‐6‐phosphate dehydrogenase (G6PD)‐deficient infants: Enzyme activity and gene variants as risk factors for phototherapy in the first week of life

Evaluation of quantitative point-of-care test for measurement of glucose-6-phosphate dehydrogenase enzyme activity in Malaysia

Molecular Characterisation of [alpha]- and [beta]-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia

Team-Based Learning: Benefits on Learning and Students’ Perception

Multiplex STR panel for assessment of chimerism following hematopoietic stem cell transplantation (HSCT)

Importance of extended blood group genotyping in multiply transfused patients

Evaluation of Glucose-6-Phosphate Dehydrogenase stability in stored blood samples

A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia

Risk Factors Associated with Unconjugated Neonatal Hyperbilirubinemia in Malaysian Neonates

Phoenix dactylifera (date fruits) administration to animal models of neurological diseases: A systematic review of health benefits

Ex vivo expanded SSEA-4+ human limbal stromal cells are multipotent and do not express other embryonic stem cell markers

Hemoglobinopathies and thalassemia screening among Senoi Orang Asli in Peninsular Malaysia

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