Results 341 to 350 of about 19,761,729 (373)
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Vasoocclusion with Homozygous Hemoglobin-C Disease
Journal of Pediatric Hematology/Oncology, 1988Hemoglobin-CC is a relatively uncommon hemoglobinopathy, seen primarily in the black population. These patients usually have a mild clinical course, without significant risk of vasoocclusive crises. There are no routine recommendations for preparation prior to surgery.
J A, Fort, J R, Graham-Pole, J, Chopik
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Priapism Associated with Hemoglobin C Trait
Journal of Urology, 2002Priapism constitutes a urological emergency in which alterations to the normal physiological process leading to penile erection result in a prolonged painful erection. One hemoglobinopathy, sickle cell anemia, is linked with priapism in 11% of cases.1 Hemoglobin C is an abnormal hemoglobin distinct from hemoglobin S, which is found in sickle cell ...
Brent R, Gibson +2 more
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The Importance of Determining Irreversibly Glycosylated Hemoglobin in Diabetics
Diabetes, 1981P. Compagnucci +5 more
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Hemoglobin C in heterozygote carriers
American Journal of Hematology, 1984B F, Cameron, D B, Smith, B, Cody
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Cell-free hemoglobin limits nitric oxide bioavailability in sickle-cell disease
Nature Medicine, 2002C. Reiter +6 more
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Rheological evaluation of hemoglobin S and hemoglobin C hemoglobinopathies.
The Journal of laboratory and clinical medicine, 1977The concept of optimum hematocrit was used to compare the rheology of bloods from patients with various hemoglobin S and hemoglobin C hemoglobinopathies. The technique involved the utilization of cone and plate viscometric data to predict average flow rates under representative physiological-fluid mechanical conditions.
F, Self, L V, McIntire, B, Zanger
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