Molecular basis of rare congenital bleeding disorders-Reference-Cited by-同舟云学术

Molecular basis of rare congenital bleeding disorders

Published:2023-05 Issue: Volume:59 Page:101029
ISSN:0268-960X
Container-title:Blood Reviews
language:en
Short-container-title:Blood Reviews

Author:

Dorgalaleh Akbar,Bahraini Mehran,Shams Mahmood,Parhizkari Fereshteh,Dabbagh Ali,Naderi Tohid,Fallah Aysan,Fazeli Alieh,Ahmadi Seyed Esmaeil,Samii Amir,Daneshi Maryam,Heydari Farshad,Tabibian Shadi,Tavasoli Behnaz,Noroozi-Aghideh Ali,Tabatabaei Tahere,Gholami Mohammad Saeed

Publisher

Elsevier BV

Subject

Oncology,Hematology

Reference151 articles.

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2. The use of prophylaxis in the treatment of rare bleeding disorders;Shapiro;Thromb Res,2020

3. A unique factor XIII mutation in southeastern Iran with an unexpectedly high prevalence: khash factor XIII;Dorgalaleh;Semin Thromb Hemost,2019

4. Gastrointestinal bleeding in congenital bleeding disorders;Samii;Semin Thromb Hemost,2022

5. Pharmacological management of rare coagulation factor deficiencies besides hemophilia;Dorgalaleh;Expert Rev Hematol,2020

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