Introduction The standard screening method for alpha thalassaemia is the examination of HbH preparation. It is labour intensive and poorly standardized. The development of a rapid strip immunochromatographic test (ICT) for haemoglobin Barts offers a fast, user friendly and cost‐effective alternative screening tool. Method A total of 180 subjects with results of the thalassaemia screen and genetic testing were included. Results of the ICT and HbH preparation were correlated with genetic results to determine the performance characteristics of the tests and the effect of mean sample age on results. Results Of 180 subjects, 111 carried alpha thalassaemia mutations and 69 participants had normal genetic results. The ICT had a sensitivit...
The coupling of Thermogravimetry (TG) in conjuction with chemometrics was investigated for the first...
Objective: To evaluate sensitivity, specificity, and positive and negative predictive value of mean ...
Background: Beta-thalassemia is a common autosomal recessive hereditary disease in the Meditertanean...
In a retrospective study of 36 cases of alpha-thalassaemia trait, 43 cases of beta-thalassaemia trai...
Beta-thalassaemia is characterized by a decrease ( +) or absence ( 0) in the synthesis of -globin ch...
Alpha-thalassemia comprises a group of inherited disorders in which alpha-hemoglobin chain productio...
α0-Thalassemia is an inherited hematological disorder caused by the deletion of α-globin genes. The ...
The α and β-thalassaemias (thal) are common genetic disorders of globin chain synthesis where the ca...
Objective: To determine the utility of the mean corpuscular hemoglobin (MCH) as a screening modality...
Aims - To compare the haemoglobin (Hb) H inclusion test with immunocytochemical detection of embryon...
Aim - To compare the haemoglobin (Hb) H inclusion test with a polymerase chain reaction CPCR) test i...
In this paper the authors report the evolution of a new automatic HPLC analyser for screening haemog...
the cause of up to 80 % of fetal hydrops in Southeast Asia, is encountered in many other countries. ...
Introduction: The aim of thalassaemia screening is to reduce thalassaemia syndromes with significant...
Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hyp...
The coupling of Thermogravimetry (TG) in conjuction with chemometrics was investigated for the first...
Objective: To evaluate sensitivity, specificity, and positive and negative predictive value of mean ...
Background: Beta-thalassemia is a common autosomal recessive hereditary disease in the Meditertanean...
In a retrospective study of 36 cases of alpha-thalassaemia trait, 43 cases of beta-thalassaemia trai...
Beta-thalassaemia is characterized by a decrease ( +) or absence ( 0) in the synthesis of -globin ch...
Alpha-thalassemia comprises a group of inherited disorders in which alpha-hemoglobin chain productio...
α0-Thalassemia is an inherited hematological disorder caused by the deletion of α-globin genes. The ...
The α and β-thalassaemias (thal) are common genetic disorders of globin chain synthesis where the ca...
Objective: To determine the utility of the mean corpuscular hemoglobin (MCH) as a screening modality...
Aims - To compare the haemoglobin (Hb) H inclusion test with immunocytochemical detection of embryon...
Aim - To compare the haemoglobin (Hb) H inclusion test with a polymerase chain reaction CPCR) test i...
In this paper the authors report the evolution of a new automatic HPLC analyser for screening haemog...
the cause of up to 80 % of fetal hydrops in Southeast Asia, is encountered in many other countries. ...
Introduction: The aim of thalassaemia screening is to reduce thalassaemia syndromes with significant...
Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hyp...
The coupling of Thermogravimetry (TG) in conjuction with chemometrics was investigated for the first...
Objective: To evaluate sensitivity, specificity, and positive and negative predictive value of mean ...
Background: Beta-thalassemia is a common autosomal recessive hereditary disease in the Meditertanean...