Ion-exchange high-performance liquid chromatography was employed as a screening method for abnormal hemoglobins in the newborn period. Samples of cord blood collected in EDTA tubes were used for this analysis. Hemolysates were injected onto 4.1 x 100-mm Synchropak ion-exchange columns using an automatic injector. Hemoglobin separation was carried out by means of a sodium acetate gradient. A total of 415 samples was analyzed. Hemoglobins A, F, and Bart's, as well as C or S when present, were separately eluted and quantitated using a 35-min gradient program. Four individuals with sickle cell disease, 26 with S or C trait, one with SC disease, and two others with alpha-chain variants were diagnosed with this method. The proportion of Bart's ...
BACKGROUND: Neonatal screening programs for sickle cell disease are now widespread in North American...
Background The birth prevalence of severe haemoglobinopathies such as sickle cell disease (SCD) in t...
Prenatal or antenatal diagnosis of sickle hemoglobinopathies is now feasible, hut it is still regard...
Ion-exchange high-performance liquid chromatography was employed as a screening method for abnormal ...
We evaluated the use of an HPLC method for screening hemoglobins in cord blood. We studied the genot...
We evaluated the use of an HPLC method for screening hemoglobins in cord blood. We studied the genot...
The use of a recently developed cation-exchange HPLC packing material for the separation of hemoglob...
Background: Newborn cord blood screening identifies infants with underlying haemoglobinopathies befo...
Hemoglobin electrophoresis of cord blood from 4,499 newborns was performed as part of a sickle cell ...
Detection and quantification of Hb subtypes of human blood is integral to presumptive identification...
Detection and quantification of Hb subtypes of human blood is integral to presumptive identification...
Sickle cell disease (SCD) and other hemoglobinopathies are a major health concern with a high burden...
We describe a method of electrophoresis of hemo-globin on cellulose acetate plates impregnated with ...
Background: Thalassemia and hemoglobinopathies are inherited red blood cell disorders found worldwid...
During routine hemoglobinopathy screening in our clinical laboratory via cation-exchange high-perfor...
BACKGROUND: Neonatal screening programs for sickle cell disease are now widespread in North American...
Background The birth prevalence of severe haemoglobinopathies such as sickle cell disease (SCD) in t...
Prenatal or antenatal diagnosis of sickle hemoglobinopathies is now feasible, hut it is still regard...
Ion-exchange high-performance liquid chromatography was employed as a screening method for abnormal ...
We evaluated the use of an HPLC method for screening hemoglobins in cord blood. We studied the genot...
We evaluated the use of an HPLC method for screening hemoglobins in cord blood. We studied the genot...
The use of a recently developed cation-exchange HPLC packing material for the separation of hemoglob...
Background: Newborn cord blood screening identifies infants with underlying haemoglobinopathies befo...
Hemoglobin electrophoresis of cord blood from 4,499 newborns was performed as part of a sickle cell ...
Detection and quantification of Hb subtypes of human blood is integral to presumptive identification...
Detection and quantification of Hb subtypes of human blood is integral to presumptive identification...
Sickle cell disease (SCD) and other hemoglobinopathies are a major health concern with a high burden...
We describe a method of electrophoresis of hemo-globin on cellulose acetate plates impregnated with ...
Background: Thalassemia and hemoglobinopathies are inherited red blood cell disorders found worldwid...
During routine hemoglobinopathy screening in our clinical laboratory via cation-exchange high-perfor...
BACKGROUND: Neonatal screening programs for sickle cell disease are now widespread in North American...
Background The birth prevalence of severe haemoglobinopathies such as sickle cell disease (SCD) in t...
Prenatal or antenatal diagnosis of sickle hemoglobinopathies is now feasible, hut it is still regard...