Results 1 to 10 of about 593,389 (220)
Archives of Internal Medicine, 1955 BY THE USE of filter-paper electrophoresis, the hematologist has gained a relatively simple and accurate method of differentiating the various abnormal or atypical hemoglobins.* Thus, we may identify normal hemoglobin (A), sickle hemoglobin (S), the combination of these (S-A) and C-hemoglobin in its homozygous (C-C) and heterozygous (C-A, C-S) states ...
Wilson H. Hartz, Steven O. Schwartz
+5 more sources
Sickle Cell—Hemoglobin C Disease [PDF]
Blood, 1963 Abstract Quantitative determinations of iron kinetics and hemoglobin synthesis were made on five patients with sickle cell-hemoglobin C disease. The anemia was mild in all patients but one who had the hemoglobin of 10.1 Gm. per cent. All patients were in a steady state during the period of this study.
E.R. Movitt +2 more
openalex +2 more sources
Clinical and Necropsy Findings in Hemoglobin C Disease [PDF]
Blood, 1957 Abstract A patient with homozygous hemoglobin C disease was observed during a five month period of time. Estimates of the rates of red cell synthesis were made prior to and during the administration of compound E. The post mortem findings and results of paper electrophoresis of myoglobin are presented.
Wallace N. Jensen +2 more
openalex +3 more sources
The relationship between nutritional status and sleep quality in Parkinson’s disease: a single tertiary center study [PDF]
Frontiers in NeurologyObjectiveTo investigate the prevalence of malnutrition, sleep disturbances, and the relationship between nutritional status and sleep quality in patients with Parkinson’s disease (PD).MethodsThe study included 168 PD patients and 102 Healthy Controls ...
Tuanfeng Yang +5 more
doaj +2 more sources
Intraerythrocytic Hemoglobin Crystals in Sickle Cell-Hemoglobin C Disease [PDF]
Blood, 1965 Abstract On 70 per cent of the blood smears from 60 cases of electrophoretically proven sickle cell-hemoglobin C disease, there is observed a misshapen erythrocyte that contains condensed hemoglobin crystals which are dark-hued, homogeneous and elongated and which have parallel sides with one end terminating in a pyramid or rounded shape.
L. W. Diggs, Ann Bell
openalex +3 more sources
Medullary Microvascular Thrombosis and Injury in Sickle Hemoglobin C Disease. [PDF]
J Am Soc Nephrol, 2016 Bissonnette ML +4 more
europepmc +2 more sources
Atypical Overt Hemorrhagic Stroke in an Adult With Sickle Cell-Hemoglobin C Disease: A Report of a Rare Case [PDF]
CureusManjrekar N +3 more
europepmc +3 more sources
Sickle Cell Hemoglobin C Disease Patient Undergoing Coronary Artery Bypass Grafting with Complete Exchange Blood Transfusion during Cardiopulmonary Bypass. [PDF]
J Extra Corpor Technol, 2018 Mullins F, Ott S, Mister N, Travis J.
europepmc +3 more sources