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Items for "thalassemia"

Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions

Background: α-Thalassemia is a worldwide disease and considered to be a major public health problem in countries within the so-called thalassemia belt...

Keywords: -globin, genotyping, reverse hybridization, thalassemia

05/2007 | Clinical Chemical Laboratory Medicine, Walter de Gruyter

Evaluation of the Bio-Rad VARIANT? II HbA ₂/HbA _1C Dual Program for measurement of hemoglobin concentrations and detection of variants

In this work data obtained on the VARIANT? II hemoglobin analyzer using the Dual Kit elution system were compared to those obtained with the ?-Thalassemia Short Program...

Keywords: hemoglobin A 2, hemoglobin F, sickle cell disease, thalassemia

04/2005 | Clinical Chemical Laboratory Medicine, Walter de Gruyter

Evaluation of a new Sebia kit for analysis of hemoglobin fractions and variants on the Capillarys^® system

We evaluated the analytical performances of the new Sebia kit for quantification of hemoglobin fractions (HbA, HbF and HbA₂) and structural hemoglobin variants on the Capillarys^® system...

Keywords: Capillarys®, capillary zone electrophoresis, hemoglobinopathies, thalassemia

03/2006 | Clinical Chemical Laboratory Medicine, Walter de Gruyter

The reduction of cholesteryl linoleate in lipoproteins: an index of clinical severity in ?-thalassemia/Hb E

Background: Oxidative modification of lipoproteins has been reported in ?-thalassemia and has been suggested to relate to atherogenesis-risk...

Keywords: cholesteryl linoleate, hypocholesterolemia, non-transferrin bound iron, oxidative stress, thalassemia

05/2006 | Clinical Chemical Laboratory Medicine, Walter de Gruyter

External quality assessment of hemoglobin A₂ measurement: data from an Italian pilot study with fresh whole blood samples and commercial HPLC systems

Background: To evaluate the extent of interlaboratory variation and accuracy in hemoglobin A₂ (HbA₂) assays, a pilot study of external quality assessment was organized among 48 Italian laboratories routinely measuring HbA₂...

Keywords: external quality assessment scheme (EQAS), hemoglobin A2, HPLC, Quality Control, thalassemia

01/2007 | Clinical Chemical Laboratory Medicine, Walter de Gruyter

A family with multiple mutations and sequence variations in the ?- and ?-globin gene clusters

Background: Usually, laboratory diagnostics of hereditary hemoglobin disorders is fairly straightforward...

Keywords: counseling, hemoglobin C, hemoglobinopathy, hereditary persistence of fetal hemoglobin, molecular diagnostics, thalassemia

09/2007 | Clinical Chemical Laboratory Medicine, Walter de Gruyter

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