Bibliography
Allison, Anthony C. 1954. Protection afforded by sicklecell trait against subtertian malarial infection. British Medical Journal 1: 290—4.
Angel, J. Lawrence. 1975. Paleoecology, paleodemography and health.
In Population, ecology and social evolution, World Anthropology Series, 167-90. Chicago.1977. Anemias of antiquity: Eastern Mediterranean. In Porotic hyperostosis: An enquiry, ed. E. Cockburn, Paleopathology Associates Monograph No. 2,1-5. Detroit.
Ascenzi, A., and P. Balistreri. 1977. Porotic hyperostosis and the problem of the origin of thalassemia in Italy. In Porotic hyperostosis: An enquiry, ed. E. Cockbum. Paleopathology Associates Monograph No. 2, 5-9. Detroit.
Beet, E. A. 1946. Sickle cell disease in the Balovale district of Northern Rhodesia. EastAfrican Medical Journal 23: 75-86.
Beutler, E. 1980. The red cell: A tiny dynamo. In Blood pure and eloquent, ed. M. W. Wintrobe, 141—68. New York.
Brain, P. 1952. Sickle cell anemia in Africa. British Medical Journal 2: 880.
Carson, Paul E., et al. 1956. Enzymatic deficiency in primaquin-sensitive erthrocytes. Science 124: 484—5.
Castle, W. B. 1980. The conquest of pernicious anemia. In Blood pure and eloquent, ed. M. W. Wintrobe, 171— 208. New York.
Conley, C. Lockhart. 1980. Sickle-cell anemia. In Blood pure and eloquent, ed. M. W. Wintrobe, 319-71. New York.
. Davidson, S., and R. Passmore. 1969. Human nutrition and dietetics. Baltimore.
Dern, R. C., et al. 1954. The hemolytic effect of primaquin. I. The localization of the drug-induced hemolytic defect in primaquin-sensitive individuals. Journal of Laboratory and Clinical Medicine 43: 303-9.
Doniach D., I. M. Roitt, and K. B. Taylor. 1963. Autoimmune phenomena in pernicious anemia: Serologic overlap with thyroiditis, thyrotoxicosis and systemic lupus erythematosus. British Medical Journal 1:1374-9.
El-Najjar, M. Y., and A. Robertson. 1976. Spongy bones in prehistoric America. Science 193: 141-3.
Evans, R. W. 1943-4. The sickling phenomenon in the blood of West African natives. Transactions of the Royal Society of Tropical Medicine and Hygiene 37: 281-6.
Guthrie, C. G., and J. G. Huck. 1923. On the existence of more than four isoagglutinin groups in human blood. Bulletin of the Johns Hopkins Hospital 34: 37—48.
Hart, Gerald D. 1980. Ancient diseases of the blood. In Blood pure and eloquent, ed. M. W. Wintrobe, 33-56. New York.
Herrick, J. B. 1910. Peculiar elongated and sickle-shaped red blood corpuscles in a case of severe anemia. Archives oflnternal Medicine 6: 517—21.
Keller, Dan. 1871. G-6-PD deficiency. Cleveland.
Lambotte-Legrand, J., and C. Lambotte-Legrand. 1955. Le Prognostic de Fanemie drapanocytaire au Congo Beige (A propos de cas de 150 decides). Annales de la Societe Belgique de Medecine Tropicale 35: 53—7.
Lanzkowsky, Philip. 1968. Radiological features of iron deficiency anemia. American Journal of Diseases of Children 116: 16—29.
Lehmann, Hermann, and R. G. Huntsman. 1974. Man’s hemoglobin. Oxford.
London, Irving. 1980. Iron and heme: Crucial carriers and catalysts. In Blood pure and eloquent, ed. M. W Wintrobe, 171-208. New York.
Mackey, J. P., and F. Vivarelli. 1954. Sickle cell anemia. British Medical Journal 1: 276.
Mason, Veme, R. 1922. Sickle cell anemia. Journal of the American Medical Association 29: 1318-20.
Pauling, Linus H., et al. 1949. Sickle cell anemia, a molecular disease. Science 110: 543-8.
Sidenstricker, Virgil P., W. A. Mulherin, and R. W. Houseal. 1923. Sickle cell anemia. Report of 2 cases in children with necropsy in one case. American Journal OfDiseases of Children 26: 132—54.
Trowell, H. C. 1945. Sickle cell anemia. East African Medical Journal 22: 34—45.
Whipple, George H., and F. S. Robsheit-Robbins. 1925. Blood regeneration in severe anemia. II. Favorable influence of liver, heart and skeletal muscle in diet. American Journal of Physiology 72: 408—18.
Wintrobe, M. W. 1985. Hematology, the blossoming of a science. Philadelphia.