The Haemoglobin (Hb) genotypes of 1672 healthy blood donors at the university of Maiduguri Teaching hospital (UMTH) during the year 1999 were analysed. Hb AA, AS and SC were detected in 78.94%, 21% and 0.06% of the donor population respectively. There is the need for strict application of Hb electrophoresis on all donor blood in order to detect rare cases of mild forms of sickle cell disease who may present as donors. All blood banks should label their blood units with the appropriate tags to indicate the Hb genotype (Hb AA or Hb AS) status of the donor; and clinicians must indicate on transfusion request forms whenever the use of Hb AA rather than HbAS blood is specifically indicated as may be the case in the management of sickle cell dise...
O Brasil apresenta alta prevalência de hemoglobina S, com nítidas diferenças regionais marcadas pelo...
Thalassaemia screening programme has been conducted in Malaysia since 2004. The aim of the programme...
Sickle Cell disease is a generic term for a group of genetic disorders characterized by the predomin...
INTRODUCTION: The normal haemoglobin is an efficient transporter of oxygen to the tissues and carbon...
Background: Voluntary non-remunerated blood donation is a strategy adopted by World Health Organizat...
Background: Voluntary non-remunerated blood donation is a strategy adopted by World Health Organizat...
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud Universit...
We examined 510 healthy people aged, 2 years to 60 years, to ascertain the predominance of sickle ce...
Background. It is estimated that one out of every three Ghanaians has hemoglobin genotype mutation. ...
Blood donation from sickle cell trait (SCT) and glucose-6-phosphate dehydrogenase (G6PD)-deficient d...
Introduction: Reduction or complete absence of ?-globin chain production may result ?-thalassemia. A...
peer reviewedBackground Prevalence of sickle cell trait is high in the Democratic Republic of Congo...
Hemoglobinopathies are the most common genetic diseases and affect a great number of individuals in ...
Structural hemoglobin (Hb) variants typically are based on a point mutation in a globin gene that pr...
Detection and quantification of Hb subtypes of human blood is integral to presumptive identification...
O Brasil apresenta alta prevalência de hemoglobina S, com nítidas diferenças regionais marcadas pelo...
Thalassaemia screening programme has been conducted in Malaysia since 2004. The aim of the programme...
Sickle Cell disease is a generic term for a group of genetic disorders characterized by the predomin...
INTRODUCTION: The normal haemoglobin is an efficient transporter of oxygen to the tissues and carbon...
Background: Voluntary non-remunerated blood donation is a strategy adopted by World Health Organizat...
Background: Voluntary non-remunerated blood donation is a strategy adopted by World Health Organizat...
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud Universit...
We examined 510 healthy people aged, 2 years to 60 years, to ascertain the predominance of sickle ce...
Background. It is estimated that one out of every three Ghanaians has hemoglobin genotype mutation. ...
Blood donation from sickle cell trait (SCT) and glucose-6-phosphate dehydrogenase (G6PD)-deficient d...
Introduction: Reduction or complete absence of ?-globin chain production may result ?-thalassemia. A...
peer reviewedBackground Prevalence of sickle cell trait is high in the Democratic Republic of Congo...
Hemoglobinopathies are the most common genetic diseases and affect a great number of individuals in ...
Structural hemoglobin (Hb) variants typically are based on a point mutation in a globin gene that pr...
Detection and quantification of Hb subtypes of human blood is integral to presumptive identification...
O Brasil apresenta alta prevalência de hemoglobina S, com nítidas diferenças regionais marcadas pelo...
Thalassaemia screening programme has been conducted in Malaysia since 2004. The aim of the programme...
Sickle Cell disease is a generic term for a group of genetic disorders characterized by the predomin...