Results 11 to 20 of about 6,788 (312)
Studies on Abnormal Hemoglobins [PDF]
Blood, 1952 Abstract 1. It could be demonstrated that of the three tested types of human hemoglobin—N (normal adult), S (sickle cell) and F (fetal)—only the reduced S compound shows tactoid and gel formation in sufficiently concentrated solutions. These physico-chemical phenomena may be used for the qualitative identification of S hemoglobin.
AMOZ I. CHERNOFF, KARL SINGER
openaire +1 more source
Cadernos de Saúde Pública, 2004 As hemoglobinopatias estão incluídas dentre as doenças hereditárias mais freqüentes nas populações humanas. Estudos realizados em diferentes regiões do Brasil têm demonstrado que as hemoglobinas anormais S e C são as mais prevalentes.
Maria Cristina Pignataro Emerenciano de Araújo +3 more
doaj +1 more source
Hematology, 2022 Hemoglobin Santa Ana [β88(F4)Leu→Pro (CTG > CCG) HBB: c.266T > C] is an unstable hemoglobin variant characterized by a substitution of the amino acid leucine by proline at the 88th position of the β-globin chain.
Li Du +8 more
doaj +1 more source
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.
core +1 more source
γA gene repeats polymorphism for the analysis of haplotypes of abnormal hemoglobins
Thalassemia Reports, 2014 Aim of this study was to analyze γ A gene repeat polymorphism for the analysis of haplotypes of hemoglobin (Hb) variants such as Hb S, Hb D-Punjab, Hb O-Arab. Sickle cell cases had mainly Benin and Arab/Indian haplotype.
Nejat Akar +3 more
doaj +1 more source
Technical and Legal Aspects of a German Pilot Study with 38,220 Participants [PDF]
, 2014 Sickle cell disease (SCD) does not occur in the indigenous German population, but with the increasing number of immigrants from countries at high risk for hemoglobinopathies, the question emerges whether or not a newborn screening program (NBS) for SCD ...
Blankenstein, Oliver +4 more
core +1 more source
CHRISMED Journal of Health and Research, 2019 Background: A significant percentage of women in India suffer from dysfunctional uterine bleeding (DUB), which has a negative impact on physical and social life.
Sayantan Sen +4 more
doaj +1 more source
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
core +1 more source
Determination of Beta Thalassemia trait and abnormal Hemoglobin variant frequency
Iberoamerican Journal of MedicineIntroduction: Hemoglobinopathies are among the most common hereditary disorders globally, classified into thalassemias and abnormal hemoglobins. Abnormal hemoglobins arise from genetic alterations like point mutations, insertions, or deletions, with Hb S,
Miraç Seher Helvacı +7 more
doaj +1 more source
Pediatric Blood &Cancer, EarlyView.ABSTRACT Introduction Pulmonary dysfunction and sleep abnormalities are common in children with sickle cell disease (SCD) and are associated with worse clinical outcomes. Whether spirometry abnormalities are associated with polysomnography (PSG) findings remains unclear.
Ammar Saadoon Alishlash +4 more
wiley +1 more source