Full text
PDF









Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BOWMAN R. L., TRANTHAM H. V., CAULFIELD P. A. An instrument and method for rapid, dependable determination of freezing point depression. J Lab Clin Med. 1954 Feb;43(2):310–315. [PubMed] [Google Scholar]
- BRUCK E. Renal function in anemia. AMA Am J Dis Child. 1953 Oct;86(4):511–512. [PubMed] [Google Scholar]
- CALCAGNO P. L., McLAVY J., KELLEY T. Glomerular filtration rate in children with sickle cell disease. Pediatrics. 1950 Jan;5(1):127–129. [PubMed] [Google Scholar]
- COOLEY J. C., PETERSON W. L., ENGEL C. E., JERNIGAN J. P. Clinical triad of massive splenic infarction, sicklemia trait, and high altitude flying. J Am Med Assoc. 1954 Jan 9;154(2):111–113. doi: 10.1001/jama.1954.02940360009003. [DOI] [PubMed] [Google Scholar]
- CROSBY W. H., MUNN J. I., FURTH F. W. Standardizing a method for clinical hemoglobinometry. U S Armed Forces Med J. 1954 May;5(5):693–703. [PubMed] [Google Scholar]
- ETTELDORF J. N., SMITH J. D., TUTTLE A. H., DIGGS L. W. Renal hemodynamic studies in adults with sickle cell anemia. Am J Med. 1955 Feb;18(2):243–248. doi: 10.1016/0002-9343(55)90239-4. [DOI] [PubMed] [Google Scholar]
- ETTELDORF J. N., TUTTLE A. W., CLAYTON G. W. Renal function studies in pediatrics. 1. Renal hemodynamics in children with sickle cell anemia. AMA Am J Dis Child. 1952 Feb;83(2):185–191. doi: 10.1001/archpedi.1952.02040060051005. [DOI] [PubMed] [Google Scholar]
- FINCH C. A., HEGSTED M., KINNEY T. D., THOMAS E. D., RATH C. E., HASKINS D., FINCH S., FLUHARTY R. G. Iron metabolism; the pathophysiology of iron storage. Blood. 1950 Nov;5(11):983–1008. [PubMed] [Google Scholar]
- GOODWIN W. E., ALSTON E. F., SEMANS J. H. Hematuria and sickle cell disease; unexplained, gross unilateral, renal hematuria in Negroes, coincident with the blood sickling trait. J Urol. 1950 Jan;63(1):79-96, illust. doi: 10.1016/S0022-5347(17)68735-4. [DOI] [PubMed] [Google Scholar]
- Hayman J. M., Shumway N. P., Dumke P., Miller M. EXPERIMENTAL HYPOSTHENURIA. J Clin Invest. 1939 Mar;18(2):195–212. doi: 10.1172/JCI101035. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KUNZ H. W., PRATT E. L., MELLIN G. W., CHEUNG M. W. Impairment of urinary concentration in sickle cell anemia. Pediatrics. 1954 Apr;13(4):352–356. [PubMed] [Google Scholar]
- McCRORY W. W., GOREN N., GORNFELD D. Demonstration of impairment of urinary concentration ability, or pitressin-resistance, in children with sickle-cell anemia. AMA Am J Dis Child. 1953 Oct;86(4):512–515. [PubMed] [Google Scholar]
- NEEL J. V. The inheritance of the sickling phenomenon, with particular reference to sickle cell disease. Blood. 1951 May;6(5):389–412. [PubMed] [Google Scholar]
- SINGER K., SINGER L. Studies on abnormal hemoglobins. VIII. The gelling phenomenon of sickle cell hemoglobin: its biologic and diagnostic significance. Blood. 1953 Nov;8(11):1008–1023. [PubMed] [Google Scholar]
- SULLIVAN B. H., Jr Danger of airplane flight to persons with sicklemia. Ann Intern Med. 1950 Feb;32(2):338–342. doi: 10.7326/0003-4819-32-2-338. [DOI] [PubMed] [Google Scholar]
- WELLS I. C., ITANO H. A. Ratio of sickle-cell anemia hemoglobin to normal hemoglobin in sicklemics. J Biol Chem. 1951 Jan;188(1):65–74. [PubMed] [Google Scholar]