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, 2014 Thalassemia is one of the most common hereditary disorders in Turkey, especially in the Mediterranean region of the country. The purpose of this study was to determine the frequency of the beta-thalassemia (beta-thal) trait and abnormal hemoglobins (Hbs)
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Balkan Journal of Medical Genetics, 2016 The prevalence of β-thalassemia (β-thal) carriers in Turkey varies according to region but in general it is 2.0%. Çanakkale is a city in the Aegean region of Turkey but no study about β-thal frequency in Çanakkale has been published to date.
Uludağ A +7 more
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A Sensitive Method for Detecting Sudunit Dissociation of Abnormal Hemoglabin [PDF]
, 1983 Dissociation of abnormal hemoglobin (HbA) by gel permeation employing Sephadex G-75 column. Equimolar solutions(5чM)of Hb A and an abnolmal hemoglobin in 0.01 M phosphate buffer, 7.00 containing 0.09 M NaCl and a trace amount of KCM, are introduced into ...
Miyaji, Takaoki +2 more
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Recombinant hemoglobins with low oxygen affinity and high cooperativity.
, 2018 By introducing an additional H-bond in the alpha(1)beta(2) subunit interface or altering the charge properties of the amino acid residues in the alpha(1)beta(1) subunit interface of the hemoglobin molecule, we have designed and expressed recombinant ...
Ching-Hsuan Tsai (5067752) +1 more
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α-Thalassemia impairs the cytoadherence of Plasmodium falciparum-infected erythrocytes. [PDF]
PLoS ONE, 2012 α-Thalassemia results from decreased production of α-globin chains that make up part of hemoglobin tetramers (Hb; α(2)β(2)) and affects up to 50% of individuals in some regions of sub-Saharan Africa.
Michael A Krause +10 more
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Abnormal hemoglobin phenotypes in carriers of mild anemia in Latin America.
, 2010 We looked for abnormal hemoglobins in blood samples sent for diagnosis of anemia. Identification of the hemoglobins was made using electrophoretic, chromatographic and molecular procedures.
Zamaro, P. J., Bonini-Domingos, C. R.
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Coexistence of Relapsing Polychondritis and Sickle Cell Disease in a Child
Case Reports in Rheumatology, 2021 Relapsing polychondritis (RP) is a rare, severe connective tissue disease of unknown etiology affecting cartilaginous and proteoglycan-rich structures in an episodic and inflammatory manner.
Bernard Ofoe Tetteh +3 more
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Revista Brasileira de Hematologia e Hemoterapia, 2015 Background: Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While screenings for beta-globin mutations are far more common, alterations affecting alpha-globin genes are usually more silent and less well known.
Elza Miyuki Kimura +9 more
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Hb Andrew-Minneapolis Variant in a Turkish Family
Turkish Journal of Hematology, 2023 Hamza Sümter +3 more
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BMC Pregnancy and Childbirth, 2022 The present study aimed at estimating the prevalence of structural hemoglobinopathies in newborn and describing the hematological and biochemical characteristics between postpartum women (PW) and their respective newborns (NB) at a public maternity ...
Roberta da Silva Brito +12 more
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