Sickle cell—hemoglobin C disease
- 1 September 1964
- journal article
- Published by Elsevier in American Journal of Obstetrics and Gynecology
- Vol. 90 (1), 136-142
- https://doi.org/10.1016/s0002-9378(16)34903-1
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
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- Effect of Normal Cells on Viscosity of Sickle-Cell BloodArchives of Internal Medicine, 1963
- HAEMOGLOBIN SC DISEASE AND MEGALOBLASTIC ANAEMIA OF PREGNANCYBJOG: An International Journal of Obstetrics and Gynaecology, 1962
- ABNORMAL HEMOGLOBINSThe American Journal of the Medical Sciences, 1961
- Pregnancy in sickle cell anemia, sickle cell-hemoglobin C disease, and variants thereofAmerican Journal of Obstetrics and Gynecology, 1959
- A Specific Chemical Difference Between the Globins of Normal Human and Sickle-Cell Anæmia HæmoglobinNature, 1956
- HYPOSTHENURIA IN SICKLE CELL ANEMIA: A REVERSIBLE RENAL DEFECTJournal of Clinical Investigation, 1956
- Studies on the Destruction of Red Blood Cells. VIII. Molecular Orientation in Sickle Cell Hemoglobin Solutions.Experimental Biology and Medicine, 1950
- A STUDY OF THE ERYTHROCYTES IN A CASE OF SEVERE ANEMIA WITH ELONGATED AND SICKLE-SHAPED RED BLOOD CORPUSCLESArchives of Internal Medicine, 1917
- PECULIAR ELONGATED AND SICKLE-SHAPED RED BLOOD CORPUSCLES IN A CASE OF SEVERE ANEMIAArchives of Internal Medicine, 1910