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Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation

Journal of human genetics, 2020-03, Vol.65 (3), p.263-270

2020

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Correction to 'Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation'

Journal of human genetics, 2020-07, Vol.65 (7), p.635-635

2020

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Extended and stable gene expression via nucleofection of MIDGE construct into adult human marrow mesenchymal stromal cells

Cytotechnology (Dordrecht), 2012-03, Vol.64 (2), p.203-216

2012

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Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays

Human mutation, 2003-01, Vol.21 (1), p.101-101

2003

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Human mesenchymal stromal cells could deliver erythropoietin and migrate to the basal layer of hair shaft when subcutaneously implanted in a murine model

Tissue & cell, 2012-08, Vol.44 (4), p.249-256

2012

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Comparison of detection of glucose-6-phosphate dehydrogenase deficiency using fluorescent spot test, enzyme assay and molecular method for prediction of severe neonatal hyperbilirubinaemia

Singapore medical journal, 2009, Vol.50 (1), p.62-67

2009

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G6PD ENZYME ACTIVITY IN NORMAL TERM MALAYSIAN NEONATES AND ADULTS USING A OSMMR2000-D KIT WITH HB NORMALIZATION

Southeast Asian journal of tropical medicine and public health, 2010-07, Vol.41 (4), p.982-988

2010

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Prenatal diagnosis of aneuploidies in amniotic fluid by multiple ligation-dependent probe amplification (MLPA) analysis

Malaysian journal of pathology, 2014-12, Vol.36 (3), p.163-168

2014

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Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice

Malaysian journal of pathology, 2011-12, Vol.33 (2), p.95-100

2011

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Prevalence of iron deficiency anaemia and thalassaemia trait among undergraduate medical students

Clinica terapeutica, 2012-07, Vol.163 (4), p.287

2012

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A study of JAK2 (V617F) gene mutation in patients with chronic myeloproliferative disorders

Clinica terapeutica, 2012, Vol.163 (2), p.109

2012

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Juvenile myelomonocytic leukaemia: a case series

Malaysian journal of pathology, 2009-12, Vol.31 (2), p.121-128

2009

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Assessment of P-gp and MRP1 activities using MultiDrugQuant Assay Kit: a preliminary study of correlation between protein expressions and its functional activities in newly diagnosed acute leukaemia patients

Malaysian journal of pathology, 2008-12, Vol.30 (2), p.87-93

2008

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Semiquantitative screening test for G6PD deficiency detects severe deficiency but misses a substantial proportion of partially-deficient females

Southeast Asian journal of tropical medicine and public health, 2003-06, Vol.34 (2), p.405-414

2003

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Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Chinese

Human mutation, 1999-10, Vol.14 (4), p.352-352

1999

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Detection of Haemoglobin S using Multiplex Ligation-Dependent Probe Amplification and Flow-through Hybridization Techniques: Experience in a Tertiary Hospital

Medicine & health (Kuala Lumpur, Malaysia), 2020-06, Vol.15 (1), p.106-118

Alauddin, Hafiza

2020

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G6PD deficiency with hemolytic anemia due to a rare gene deletion-A report of the first case in Malaysia

Hematology (Luxembourg), 2006-04, Vol.11 (2), p.113-118

2006

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Expression of multidrug resistance (MDR) proteins and in vitro drug resistance in acute leukemias

Hematology (Luxembourg), 2007-02, Vol.12 (1), p.33-37

2007

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Assessing donor chimerism using flow cytometry in paroxysmal nocturnal haemoglobinuria after stem cell transplantation--a case report

Malaysian journal of pathology, 2006-12, Vol.28 (2), p.107-112

2006

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Glucose‐6‐phosphate dehydrogenase (G6PD) variants in Malaysian Malays

Human mutation, 2003-01, Vol.21 (1), p.101-101

2003

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Allogeneic haemopoietic stem cell transplantation using non-myeloablative conditioning--a local experience

Medical journal of Malaysia, 2003-06, Vol.58 (2), p.229-235

2003

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G6PD enzyme activity in normal term neonates and adults using OSMMR-D kit with HB normalisation

Pathology, 2009-01, Vol.41, p.75-75

2009

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Newborn screening of G6PD variants using long term storage of dried blood spot

Pathology, 2009-01, Vol.41, p.83-83

2009

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Prevalence of UGT1A1 mutations in malay neonates with severe jaundice

Pathology, 2009-01, Vol.41, p.68-68

2009

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Flow cytometric analysis of intracellular myeloperoxidase distinguishes lymphocytes, monocytes and granulocytes

Malaysian journal of pathology, 1998-12, Vol.20 (2), p.91-94

1998

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Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation

Correction to 'Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation'

Extended and stable gene expression via nucleofection of MIDGE construct into adult human marrow mesenchymal stromal cells

Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays

Human mesenchymal stromal cells could deliver erythropoietin and migrate to the basal layer of hair shaft when subcutaneously implanted in a murine model

Comparison of detection of glucose-6-phosphate dehydrogenase deficiency using fluorescent spot test, enzyme assay and molecular method for prediction of severe neonatal hyperbilirubinaemia

G6PD ENZYME ACTIVITY IN NORMAL TERM MALAYSIAN NEONATES AND ADULTS USING A OSMMR2000-D KIT WITH HB NORMALIZATION

Prenatal diagnosis of aneuploidies in amniotic fluid by multiple ligation-dependent probe amplification (MLPA) analysis

Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice

Prevalence of iron deficiency anaemia and thalassaemia trait among undergraduate medical students

A study of JAK2 (V617F) gene mutation in patients with chronic myeloproliferative disorders

Juvenile myelomonocytic leukaemia: a case series

Assessment of P-gp and MRP1 activities using MultiDrugQuant Assay Kit: a preliminary study of correlation between protein expressions and its functional activities in newly diagnosed acute leukaemia patients

Semiquantitative screening test for G6PD deficiency detects severe deficiency but misses a substantial proportion of partially-deficient females

Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Chinese

Detection of Haemoglobin S using Multiplex Ligation-Dependent Probe Amplification and Flow-through Hybridization Techniques: Experience in a Tertiary Hospital

G6PD deficiency with hemolytic anemia due to a rare gene deletion-A report of the first case in Malaysia

Expression of multidrug resistance (MDR) proteins and in vitro drug resistance in acute leukemias

Assessing donor chimerism using flow cytometry in paroxysmal nocturnal haemoglobinuria after stem cell transplantation--a case report

Glucose‐6‐phosphate dehydrogenase (G6PD) variants in Malaysian Malays

Allogeneic haemopoietic stem cell transplantation using non-myeloablative conditioning--a local experience

G6PD enzyme activity in normal term neonates and adults using OSMMR-D kit with HB normalisation

Newborn screening of G6PD variants using long term storage of dried blood spot

Prevalence of UGT1A1 mutations in malay neonates with severe jaundice

Flow cytometric analysis of intracellular myeloperoxidase distinguishes lymphocytes, monocytes and granulocytes

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