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1979 2
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Priapism and Sickle Cell Disease: Special Considerations in Etiology, Management, and Prevention.
Ahuja G, Ibecheozor C, Okorie NC, Jain AJ, Coleman PW, Metwalli AR, Tonkin JB. Ahuja G, et al. Urology. 2021 Oct;156:e40-e47. doi: 10.1016/j.urology.2021.06.010. Epub 2021 Jun 26. Urology. 2021. PMID: 34181970 Review.
SCD priapism is caused by sickled erythrocytes obstructing venous outflow and can lead to permanent erectile dysfunction. This article reviews the pathology, physiology, and management of SCD priapism, including potential novel therapeutic agents....
SCD priapism is caused by sickled erythrocytes obstructing venous outflow and can lead to permanent erectile dysfunction. This …
Sickled erythrocytes, hyphema, and secondary glaucoma: I. The diagnosis and treatment of sickled erythrocytes in human hyphemas.
Goldberg MF. Goldberg MF. Ophthalmic Surg. 1979 Apr;10(4):17-31. Ophthalmic Surg. 1979. PMID: 460814
Four patients with sickle cell hemoglobinopathies (one SC, three AS) and hyphemas were found to have more erythrocytes sickled in their anterior chambers than in their circulating venous blood. ...
Four patients with sickle cell hemoglobinopathies (one SC, three AS) and hyphemas were found to have more erythrocytes sickled
The diagnosis and treatment of secondary glaucoma after hyphema in sickle cell patients.
Goldberg MF. Goldberg MF. Am J Ophthalmol. 1979 Jan;87(1):43-9. doi: 10.1016/0002-9394(79)90190-9. Am J Ophthalmol. 1979. PMID: 434052
Four patients with sickle cell hemoglobinopathies (one sickle cell hemoglobin C disease (SC); three sickle cell trait (AS)) and hyphemas had a higher percentage of erythrocytes sickled in their anterior chambers than in their circulating venous blood. ...
Four patients with sickle cell hemoglobinopathies (one sickle cell hemoglobin C disease (SC); three sickle cell trait (AS)) and hyphemas had …
The management of hematuria associated with sickle hemoglobinopathies.
McInnes BK 3rd. McInnes BK 3rd. J Urol. 1980 Aug;124(2):171-4. doi: 10.1016/s0022-5347(17)55360-4. J Urol. 1980. PMID: 7401225
Hematuria secondary to sickle cell hemoglobinopathy was first reported by Abel and Brown in 1948. They noted sickled erythrocytes in a kidney removed for suspected tumor. Since then there have been numerous reports attributing hematuria to the abnormal hemoglobins t …
Hematuria secondary to sickle cell hemoglobinopathy was first reported by Abel and Brown in 1948. They noted sickled erythrocytes