A large case series on surgical outcomes in congenital factor XIII deficiency patients in Iran
Author:
Affiliation:
1. Genetics of Non Communicable Disease Research Center; Zahedan University of Medical Sciences; Zahedan Iran
2. Hematology Research Center; Shiraz University of Medical Sciences; Shiraz Iran
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.13872/fullpdf
Reference27 articles.
1. The rare coagulation disorders-review with guidelines for management from the United Kingdom Haemophilia Centre Doctors’ Organisation;Bolton-Maggs;Haemophilia,2004
2. Novel aspects of factor XIII deficiency;Muszbek;Curr Opin Hematol,2011
3. Delayed umbilical bleeding-a presenting feature for factor XIII deficiency: clinical features, genetics, and management;Anwar;Pediatrics,2002
4. International registry on factor XIII deficiency: a basis formed mostly on European data;Ivaskevicius;Thromb Haemost,2007
5. Factor XIII deficiency;Karimi;Semin Thromb Hemost,2009
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1. Synchronous duodenal neuroendocrine neoplasm and congenital factor XIII deficiency: case report and review of the literature;Annals of Translational Medicine;2022-08
2. The use of prophylaxis in the treatment of rare bleeding disorders;Thrombosis Research;2020-12
3. Factor XIII deficiency leading to preseptal haematoma post-strabismus surgery;BMJ Case Reports;2019-11
4. A Unique Factor XIII Mutation in Southeastern Iran with an Unexpectedly High Prevalence: Khash Factor XIII;Seminars in Thrombosis and Hemostasis;2019-01-10
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