REFERENCES
- Selwyn, J. G. and Dacie, J. V.: Autohemolysis and other changes resulting from the incubation in vitro of red cells from patients with congenital hemolytic anemia. Blood 9: 414, 1954.
- de Gruchy, G. G, Crawford, H. and Morton, D.: Atypical (nonspherocytic) congenital hemolytic anaemia. VII Congressu Societatis Internationalis Haematologiae, 1958, p. 425.
- Zinkham, W. H. and Lenhard, R. E.: Metabolic abnormalities of erythrocytes of patients with congenital nonspherocytic hemolytic anemia. J Pediat 55: 319, 1959.
- Valentine, W. N., Tanaka, K. R. and Miwa, S.: A specific erythrocyte glycolytic enzyme defect (pyruvate kinase) in three subjects with congenital non-spherocytic hemolytic anemia. Trans Ass Amer Physicians 74: 100, 1961.
- LÖhr, G. W. and Waller, H. D.: Eine neue enzymopenishe hamolytische Anämie mit Glutathion- reduktase-Mangel. Med Klin 57: 1521, 1962.
- Bowdler, A. J. and Prankerd, T. A. J.: Studies in congenital nonspherocytic haemolytic anaemias with special enzyme defects. Acta Haemat 31: 65, 1964.
- Schneider, A. S., Valentine, W. N., Hattori, M. and Heins, H. L.: Hereditary hemolytic anemia with triosephosphate isomerase deficiency. New Eng J Med 272: 229, 1965.
- Zinkham, W. H., Lenhard, R. E and Childs, B.: A deficiency of glucose-6-phosphate dehydrogenase activity in erythrocytes from patients with favism. Bull Hopkins Hosp 102: 169, 1958.
- Bucher, T. and Pfleiderer, G.: Pyruvate-kinase from muscle. In Colowick, S. P. and Kaplan, N. O. (Editors): Methods in Enzymology. New York, Academic Press Inc., 1955, vol. 1, p. 435.
- Tarlov, A. R., Brewer, G. J., Carson, P. E. and Alving, A. S.: Primaquine sensitivity. Arch Intern Med 109: 209, 1962.
- Gross, R. T.: Clinical applications of some recent studies of erythrocyte enzymes. Bull NY Acad Med 39: 90, 1963.
- Lindenbaum, J. and Klipstein, F. A.: Folic acid deficiency in sickle-cell anemia. New Eng J Med 269: 875, 1963.
- Shahidi, N. T. and Diamond, L. K.: Enzyme deficiency in erythrocytes in congenital nonspherocytic hemolytic anemia. Pediatrics 24: 245, 1959
- Kirkman, H. N. and Riley, H. D.: Congenital nonspherocytic hemolytic anemia. Amer J Dis Child 102: 313, 1961.
- Tanaka, K. R., Valentine, W. N. and Miwa, S.: Pyruvate kinase (PK) deficiency hereditary non-spherocytic hemolytic anemia. Blood 19: 267, 1962.
- Oski, F. A. and Diamond, L. K.: Erythrocyte pyruvate kinase deficiency resulting in congenital nonspherocytic hemolytic anemia. Ibid.,12 p. 763
- Beutler, E.: The hemolytic effect of primaquine and related compounds: A review. Blood 14: 103, 1959.
- Doxiadis, S. A., Fessas, P., Valaes, T. and Mastrokalos, N.: Glucose-6-phosphate dehydrogenase deficiency, a new aetiological factor of severe neonatal jaundice. Lancet 1: 297, 1961.