Results 41 to 50 of about 4,456 (190)
Revista Brasileira de Hematologia e Hemoterapia, 2007 Há vários tipos de hemoglobinopatias que são caracterizados por variantes das hemoglobinas anormais (ex: Hb S, Hb C, Hb Instáveis,etc) e por talassemias (ex: tal. alfa, tal.
Paulo Cesar Naoum +1 more
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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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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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THALASSEMIA RESEARCH AND ABNORMAL HEMOGLOBINS
Annals of the New York Academy of Sciences, 1969 H. Lehmann, R. G. Huntsman
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Abnormal hemoglobins in mauritius Island
American Journal of Hematology, 1995 Rolande Ducrocq +11 more
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THE MANIFESTATIONS OF ABNORMAL HEMOGLOBINS OF MAN: HEMOGLOBINS M *
Annals of the New York Academy of Sciences, 1974 Phillip D. Pulsinelli
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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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