Browsing ODA Open Digital Archive by Author "Klingenberg, Olav"
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Hb Aalesund (HBA2: c.400_406delAGCACCG), an Unstable α-Globin Variant Found in a Norwegian Patient Causing Moderate Hemolytic Anemia and Falsely High Hb A1c Using Ion Exchange High Performance Liquid Chromatography.
Grimholt, Runa Marie; Fjeld, Bente; Selsås, Hilde; Schwettmann, Lutz; Klingenberg, Olav (Hemoglobin;Volume 43, Issue 2, Journal article; Peer reviewed, 2019-04-03)A new unstable hemoglobin (Hb) variant, named Hb Aalesund, was detected during Hb A1c measurement in a patient with a nearly compensated hemolytic anemia. Sequencing of the α-globin genes revealed a 7 bp deletion in exon ... -
Hemoglobinopathy gone astray—three novel forms of α-thalassemia in Norwegian patients characterized by quantitative real-time PCR and DNA sequencing
Grimholt, Runa Marie; Fjeld, Bente; Klingenberg, Olav (Scandinavian Journal of Clinical and Laboratory Investigation;Volume 81, 2021 - Issue 8, Peer reviewed; Journal article, 2021-11-18)α-thalassemia is one of the most common monogenic diseases worldwide and is caused by reduced or absent synthesis of α-globin chains, most commonly due to deletions of one or more of the α-globin genes. α-thalassemia occurs ...