Karl Singer, M.D.
Affiliations: | Hematologic Research | Michael Reese Hospital, Chicago, IL, United States |
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"Karl Singer"Mean distance: 17.86 (cluster 32)
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Publications
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| Singer K, Ramot B. (1956) Pseudohemophilia Type B: Hereditary Hemorrhagic Diathesis Characterized by Prolonged Bleeding Time and Decrease in Antihemophilic Factor Jama Internal Medicine. 97: 715-725 |
| Ramot B, Singer K, Heller P, et al. (1956) Hageman factor (HF) deficiency. Blood. 11: 745-752 |
| Ramot B, Angelopoulos B, Singer K. (1955) Plasma thromboplastin antecedent deficiency. Jama Internal Medicine. 95: 705-712 |
| Singer K, Singer L, Goldberg SR. (1955) Studies on abnormal hemoglobins. XI. Sickle cell-thalassemia disease in the Negro; the significance of the S+A+F and S+A patterns obtained by hemoglobin analysis. Blood. 10: 405-415 |
| Singer K, Angelopoulos B, Ramot B. (1955) Studies on human myoglobin. I. Myoglobin in sickle cell disease. Blood. 10: 979-986 |
| MOTULSKY AG, SINGER K, CROSBY WH, et al. (1954) The life span of the elliptocyte; hereditary elliptocytosis and its relationship to other familial hemolytic diseases. Blood. 9: 57-72 |
| Singer K, Fisher B. (1953) Studies on abnormal hemoglobins. VII. The composition of the non-S hemoglobin fraction in sickle-cell anemia bloods; a comparative quantitative study by the methods of electrophoresis and alkali denaturation. Journal of Laboratory and Clinical Medicine. 42: 193-204 |
| SINGER K, FISHER B. (1953) Studies on Abnormal Hemoglobins Blood. 8: 270-275 |
| Singer K, Singer L. (1953) Studies on Abnormal Hemoglobins VIII. The Gelling Phenomenon of Sickle Cell Hemoglobin: Its Biologic and Diagnostic Significance Blood. 8: 1008-1023 |
| Singer K, Fisher B, Perlstein MA. (1952) Acanthrocytosis; a genetic erythrocytic malformation. Blood. 7: 577-591 |