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Clinicopathological study of dentigerous cysts in Singapore and Malaysia.
This was a retrospective study of dentigerous cysts in people from the Singapore-Malaysian region. The purpose of this study was to present the clinicopathologic features of dentigerous cysts in theExpand
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Seroprevalence of hepatitis C virus infection among blood donors in a teaching hospital in northeastern Malaysia.
The aim of this study was to determine the prevalence of HCV infection and the signal/cutoff (S/CO) value for false reactive, false positive, indeterminate and true positive HCV infection amongExpand
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Detection of Common Deletional Alpha-Thalassemia Spectrum by Molecular Technique in Kelantan, Northeastern Malaysia
Thalassemia is a hereditary blood disorder that results from genetic defects causing deficient synthesis of hemoglobin polypeptide chains. Although thalassemia mostly affects developing countries,Expand
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Exophytic Verrucous Hyperplasia of the Oral Cavity – Application of Standardized Criteria for Diagnosis from a Consensus Report
Verruco-papillary lesions (VPLs) of the oral cavity described in the literature involve a spectrum of conditions including squamous papilloma, verruca vulgaris, focal epithelial hyperplasia,Expand
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An Audit on Near-Miss Events in Transfusion Medicine: The Experience of the Teaching Hospital in Northeastern Malaysia
The rate of near misses in transfusion is important as it indicates situations with the potential of adverse outcome. The aim of this study was to assess the frequency of mislabeled and miscollectedExpand
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Immunoglobulin Heavy Chain Gene Rearrangement in Non B-cell Haematological Malignancies.
OBJECTIVE Clonality detection through amplifying immunoglobulin heavy chain (IGH) gene rearrangements by polymerase chain reaction (PCR) is a useful tool in diagnosis of various B-lymphoidExpand
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The Level of Natural Anticoagulants in Transfusion Dependent Thalassemia Patients in Kelantan, Northeastern Malaysia
The association of the severe form of thalassemia with complications of blood transfusion, iron overload, bony deformity and gall stone is well described. Currently, due to improvement in the way ofExpand
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Acquired haemophilia a in a postpartum patient: diagnosis and management
Acquired haemophilia A is a potentially life threatening haemorrhagic disorder caused by spontaneous occurrence of autoantibodies directed against coagulation factor VIII. It has a mortality rate ofExpand
Detection of CommonDeletional Alpha-Thalassemia Spectrum byMolecular Technique in Kelantan , NortheasternMalaysia
Thalassemia is a hereditary blood disorder that results from genetic defects causing deficient synthesis of hemoglobin polypeptide chains. Although thalassemia mostly affects developing countries,Expand
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