Inhibitor; An Uncommon But Vexing Challenge In North Indian Patients With Hemophilia A
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12288-022-01539-9.pdf
Reference16 articles.
1. Stonebraker JS, Bolton-Maggs PHB, Brooker M, Evatt B, Iorio A, Makris M et al (2020) The world federation of hemophilia annual global Survey 1999–2018. Haemophilia 26:591–600. https://doi.org/10.1111/hae.14012
2. Srivastava A, Santagostino E, Dougall A, Kitchen S, Sutherland M, Pipe SW et al (2020) WFH guidelines for the management of hemophilia, 3rd edition. Haemoph Off J World Fed Hemoph 26:1–158. https://doi.org/10.1111/hae.14046
3. Gunasekera D, Ettinger RA, Fletcher SN, James EA, Liu M, Barrett JC et al (2015) Factor VIII gene variants and inhibitor risk in African American hemophilia A patients. Blood 126:895–904. https://doi.org/10.1182/blood-2014-09-599365
4. Hay CRM (2006) The epidemiology of factor VIII inhibitors. Haemophilia 12:23–29. https://doi.org/10.1111/j.1365-2516.2006.01362.x
5. Pinto P, Shelar T, Nawadkar V, Mirgal D, Mukaddam A, Nair P et al (2014) The Epidemiology of FVIII Inhibitors in Indian Haemophilia A Patients. Indian J Hematol Blood Transfus 30:356–363. https://doi.org/10.1007/s12288-014-0342-z
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