Frequency of silent brain lesions and aspirin protection evaluation over 3 years follow-up in beta thalassemia patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00277-019-03765-0.pdf
Reference21 articles.
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2. Wong V, Yu Y, Liang R, Tso W, Li A, Chan T (1990) Cerebral thrombosis in beta-thalassemia/hemoglobin E disease. Stroke 21(5):812–816
3. Taher AT, Musallam KM, Karimi M, El-Beshlawy A, Belhoul K, Daar S, Saned M-S, El-Chafic A-H, Fasulo MR, Cappellini MD (2010) Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity: the OPTIMAL CARE study. Blood 115(10):1886–1892
4. Karimi M, Cohan N, De Sanctis V, Mallat NS, Taher A (2014) Guidelines for diagnosis and management of Beta-thalassemia intermedia. Pediatr Hematol Oncol 31(7):583–596
5. Eldor A, Rachmilewitz EA (2002) The hypercoagulable state in thalassemia. Blood 99(1):36–43
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