Oral tranexamic acid as a novel treatment option for persistent haematuria in patients with sickle cell disease-Reference-Cited by-同舟云学术

Oral tranexamic acid as a novel treatment option for persistent haematuria in patients with sickle cell disease

Published:2010-04-01 Issue:11 Volume:89 Page:1179-1180
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Davis Niall F.,McGuire Barry B.,Lawlor Leo,O’Gorman Peter,O’Malley Kiaran J.,Fitzpatrick John M.

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00277-010-0936-y.pdf

Reference8 articles.

1. Bennett MA, Heslop RW, Meynell MJ (1967) Massive haematuria associated with sickle-cell trait. Br Med J 1:677–679

2. Mostofi FK, Vorder Brueege CF, Diggs LW (1957) Lesions in kidneys removed for unilateral hematuria in sickle-cell disease. AMA Arch Pathol 63:336–351

3. Lucas WM, Bullock WH (1960) Hematuria in sickle cell disease. J Urol 83:733–741

4. Harrow BR, Sloane JA, Liebman NC (1963) Roentgenologic demonstration of renal papillary necrosis in sickle-cell trait. N Engl J Med 268:969–976

5. Immergut MA, Stevenson T (1965) The use of epsilon amino caproic acid in the control of hematuria associated with hemoglobinopathies. J Urol 93:110–111

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