REFERENCES
- Emond A. M., Holman R., Hayes R. J., Serjeant G. R. Priapism and Impotence in Homozygous Sickle Cell Disease. Arch. Inter. Med. 1980; 140: 1434–1437
- Fowler J. E., Koshy M., Strub M., Chinn K. Priapism Associated with the Sickle Cell Hemoglobinopathies: Prevalence, Natural History and Sequelae. J. Urol. 1991; 145: 65–68
- Mantadakis E., Cavender J. D., Rogers Z. R., Ewalt D. H., Buchanan G. R. Prevalence of Priapism in Children and Adolescents with Sickle Cell Anemia. J. Pediatr. Hematol. Oncol. 1999; 21(6)518–522
- Al-Awamy B., Taha S. A., Naeem M. A. Priapism in Association with Sickle Cell Anemia in Saudi Arabia. Acta Haematol 1985; 73: 181–182
- Waincoast J. S., Bell J. I., Thein S. L., Higgs D. R., Sergeant G. R., Peto T. E., Weatherall D. J. Multiple Origins of the Sickle Mutation: Evidence from βs Globin Gene Cluster Polymorphisms. Mol. Biol. Med. 1983; 1: 191–197
- Ségbena A. Y., Prehu C., Wajcman H., Bardakdjian-Michau J., Messie K., Ketefe L., Vovor A., David M., Feingold J., Galacteros F. Hemoglobins in Togolese Newborns: Hb S, Hb C, Hb Bart's, and α-Globin Gene Status. Am. J. Hematol. 1998; 59: 208–213
- Hamre M. R., Harmon E. P., Kirkpatrick D. V., Stern M. J., Humbert J. R. Priapism as a Complication of Sickle Cell Disease. J. Urol. 1991; 145: 1–5
- Kaplan E. L., Meier P. Nonparametric Estimation from Incomplete Observations. J. Am. Stat. Assoc. 1958; 53: 457–481
- Taha S. A., Sharayah A., Salem A., Knox-Macaulay H. Homozygous Sickle Cell Disease and Priapism in the Eastern Province of Saudi Arabia. Acta Haematol 1987; 77: 60–61
- Pohl J., Pott B., Kleinhans G. Priapism: A Three-Phase Concept of Management According to Aetiology and Prognosis. Br. J. Urol. 1986; 58: 113–118
- Winter C. C., McDowell G. Experience with 105 Patients with Priapism: Update Review of all Aspects. J. Urol. 1988; 140: 980–983