Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cells
We describe three mutations of the red-cell anion exchanger band 3 (AE1, SLC4A1) gene
associated with distal renal tubular acidosis (dRTA) in families from Malaysia and Papua New …
associated with distal renal tubular acidosis (dRTA) in families from Malaysia and Papua New …
[HTML][HTML] Glucose-6-Phosphate dehydrogenase deficiency and neonatal hyperbilirubinemia: Insights on pathophysiology, diagnosis, and gene variants in disease …
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a prevalent condition worldwide
and is caused by loss-of-function mutations in the G6PD gene. Individuals with deficiency …
and is caused by loss-of-function mutations in the G6PD gene. Individuals with deficiency …
[PDF][PDF] Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM Medical Centre
Alpha (α) thalassaemia is the most common inherited disorder in Malaysia. The clinical
severity is dependant on the number of α genes involved. Full blood count (FBC) and …
severity is dependant on the number of α genes involved. Full blood count (FBC) and …
GIS based multi-criteria decision making for landslide hazard zonation
AN Othman, WM Naim, S Noraini - Procedia-Social and Behavioral …, 2012 - Elsevier
Growing population and expansion of settlements over hilly areas have largely increased
the impact of natural disasters such as landslide. This paper deals with the use of …
the impact of natural disasters such as landslide. This paper deals with the use of …
Complete molecular characterisation of glucose-6-phosphate dehydrogenase (G6PD) deficiency in a group of Malaysian Chinese neonates.
We performed DNA analysis on cord blood samples of 128 Chinese male neonates diagnosed
as G6PD deficiency in Hospital Universiti Kebangsaan Malaysia by a combination PCR-…
as G6PD deficiency in Hospital Universiti Kebangsaan Malaysia by a combination PCR-…
Population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review
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 …
hereditary disorder and a global public health concern that is most prevalent in malaria-endemic …
Importance of extended blood group genotyping in multiply transfused patients
Blood group antigen systems are not limited to the ABO blood groups. There is increasing
interest in the detection of extended blood group systems on the red cell surface. The …
interest in the detection of extended blood group systems on the red cell surface. The …
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 in …
Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] is a rare hemoglobin (Hb) variant due
to a mutation at codon 59 of the α2- or α1-globin gene resulting in a glycine to aspartic acid …
to a mutation at codon 59 of the α2- or α1-globin gene resulting in a glycine to aspartic acid …
Risk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates
Objective: To investigate the risk factors associated with neonatal hyperbilirubinemia in
Malaysian neonates. Methods: A prospective study was conducted to investigate the effects of …
Malaysian neonates. Methods: A prospective study was conducted to investigate the effects of …
Prevalence and molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Senoi Malaysian Orang Asli population
…, SNB Mohd Noor, N Zakaria, A Othman… - Plos one, 2023 - journals.plos.org
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder
characterized by reduced G6PD enzyme levels in the blood. This condition is common in …
characterized by reduced G6PD enzyme levels in the blood. This condition is common in …
