Results 31 to 40 of about 6,312 (138)
Tractional Retinal Detachment Related to Hemoglobin C Trait Retinopathy: A Case Report
Türk Oftalmoloji Dergisi, 2023 Hemoglobin C (HbC) disease is an uncommon disease that is generally considered benign, causing only occasionally painless hematuria, osteomyelitis, and dental abnormalities. Ocular manifestations have rarely been described in these patients.
Xavier Garrell-Salat +5 more
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Hemoglobin C/Korle-Bu Identified In A Patient With A Previous Diagnosis Of Hemoglobin S/C Disease [PDF]
American Journal of Clinical Pathology, 2020 Abstract Casestudy Hemoglobin Korle-Bu (Hb-KB) is an uncommon Hb variant that can be mistaken for Hb-S on electrophoretic screening. While Hb-KB alone has no clinical manifestations, there are only limited case studies describing KB in combination with other Hb variants.
Henry M. Rinder +3 more
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Revista Cubana de Investigaciones Biomédicas, 1998 Se ensayó una nueva técnica macrocromatográfica en carboximetilcelulosa y amortiguador imidazol-HCl-KCN-NaCl a pH 6,7. La técnica es confiable y exacta para la separación y cuantificación de hemoglobina A2 en individuos portadores de hemoglobina AC, Cb ...
Jorge Cabrera Llano +2 more
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Low proportions of glycosylated hemoglobin associated with hemoglobin S and hemoglobin C.
Clinical Chemistry, 1979 Abstract Using a cation-exchange chromatographic method, we found normal or subnormal values for glycosylated hemoglobin in a few diabetic patients with persistent hyperglycemia. Subsequent investigations revealed that these unexpected results had originated from black patients with diabetes.
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Some Characteristic Properties of Hemoglobin C [PDF]
Blood, 1955 Abstract 1. The present paper describes an apparently white family in which a few members suffered from homozygous and heterozygous hemoglobin C disease. Since the paternal great grandfather and the maternal grandfather of the patients examined were in a family relation of the first order, it is surmised that the hemoglobin C was derived
P. C. Van Der Schaaf +2 more
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Revista Brasileira de Hematologia e Hemoterapia, 2009 A hemoglobina C (Hb C) é originária do oeste da África e é detectada por migração lenta na eletroforese alcalina em acetato de celulose. Consiste na mutação do gene da globina beta no códon 6 (GAG-AAG), resultando na substituição do sexto aminoácido da ...
Ivan L. Angulo, Sandra B. R. Picado
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Revista Brasileira de Hematologia e Hemoterapia, 2013 OBJECTIVE: To characterize alpha-chain variant hemoglobins with electric mobility similar to that of hemoglobin S in a newborn screening program. METHODS: βS allele and alpha-thalassemia deletions were investigated in 14 children who had undefined ...
Marcilene Rezende Silva +4 more
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BMC Research Notes, 2018 Objectives Sickle cell anemia is due to a mutations on the betaglobin gene, inducing abnormal hemoglobin. In West Africa the main mutations lead to S or C types of hemoglobin.
Stephane Koui Tossea +8 more
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Associated Effect of SLC40A1 and TMPRSS6 Polymorphisms on Iron Overload
Metabolites, 2022 Mutations in the ferroportin (FPN) gene SLC40A1 alter iron recycling and cause disturbances in iron homeostasis. The variants of TMPRSS6 contribute to the development of iron deficiencies.
Lorena Duca +5 more
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Hemoglobin Levels and Nutrients Intake on Young Soccer Athletes in Yogyakarta
Active: journal of physical education, sport, health and recreation, 2019 The purpose of this study was to know the relationship of nutrients intake and hemoglobin levels in young soccer athletes. This research was an analytical descriptive research with cross-sectional approach.
Yuni Afriani, Desty Ervira Puspaningtyas
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