STUDIES ON ABNORMAL HEMOGLOBIN
Nihon Naika Gakkai Zasshi, 1967 本邦では1957年ごろより異常血色素の本格的検索がはじめられたが,著者は戦後わが国に残された混血児達により,従来本邦に存在しなかつた異常血色素の遺伝因子が導入される可能性を考え,その実態を明らかにせんとして混血児179名について異常血色素の検索を行ない,また同時に東京,神奈川在住本邦人3000余名についても異常血色素の検索を行なつた.その結果,本邦人3000余名中よりは1例も異常血色素を確認できなかつたが,混血児179名中よりは2例に異常血色素を確認した.この比率は約1.1%である.
H Mamiya
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"Pseudo-Abnormal" Hemoglobins [PDF]
Blood, 1961 Abstract Three examples of artefactual "pseudo-abnormal" hemoglobins were observed in the course of starch block electrophoresis analysis of over 400 specimens. In fresh samples from the same patients, these components were no longer demonstrable.
Sanford L. Leikin +2 more
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In vitro determination of hemoglobin A1c for diabetes diagnosis and management: technology update [PDF]
, 2014 It is fascinating to consider the analytical improvements that have occurred since glycated hemoglobin was first used in routine clinical laboratories for diabetes monitoring around 1977; at that time methods displayed poor precision, there were no ...
English, Emma +2 more
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Severe Hemolytic Anemia due to De novo Hemoglobin Sabine in an argentinian newborn: first case in South America [PDF]
, 2015 Hemoglobin (Hb) Sabine is an unstable Hb variant that causes hemolytic anemia in heterozygous state, with inclusion bodies in the red blood cells (RBC). This hemoglobin is the result of a point mutation at codon 91(CTG)(CCG) of the beta-globin gene.
Acosta, Irma +9 more
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Validation and determination of a reference interval for Canine HbA1c using an immunoturbidimetric assay [PDF]
, 2017 Background: Hemoglobin A1c (HbA1c) provides a reliable measure of glycemic control over 2–3 months in human diabetes mellitus. In dogs, presence of HbA1c has been demonstrated, but there are no validated commercial assays. Objective: The purpose
Goemans, Anne F. +2 more
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Chemical Characterization and Subunit Hybridization of Human Hemoglobin H and Associated Compounds [PDF]
, 1963 Two abnormal hemoglobin components have been detected in association with thalassemiahemoglobin H disease. These components, as well as the major hemoglobin component, have been chemically characterized by determination of the amino acid composition, N ...
Jones, Richard T., Schroeder, W. A.
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Spleen histology in children with sickle cell disease and hereditary spherocytosis: Hints on the disease pathophysiology [PDF]
, 2016 open2Hereditary spherocytosis (HS) and sickle cell disease (SCD) are associated with splenomegaly and spleen dysfunction in pediatric patients. Scant data exist on possible correlations between spleen morphology and function in HS and SCD.
Alaggio Rita +10 more
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Evidence for multiple structural genes for the γ chain of human fetal hemoglobin [PDF]
, 1968 A sequence with a specific residue at each position was proposed for the γ chain of human fetal hemoglobin by Schroeder et al. (1) after a study in which hemoglobin from a number of individual infants was used.
Dozy, Andrée M. +6 more
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Laboratory Diagnosis of β-Thalassemia and HbE [PDF]
, 2020 β-Thalassemia and HbE, each, is a syndrome resulted from quantitative and qualitative defects of β-globin chain, respectively. In addition to history retrieve and physical examination, diagnosis of these disorders requires laboratory information ...
Tatu, Thanusak
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Studies on the Hemoglobin of Cooley's Anemia and Cooley's Trait [PDF]
, 1952 The diseases sickle cell anemia and Cooley's anemia (also known as thalassemia or Mediterranean anemia) have associated with them "minor" or "trait" forms of the disease in which the symptomatology is minimal, and the abnormalities in the red cells are ...
Rich, Alexander
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