Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia-Reference-Cited by-同舟云学术

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Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia

Published:2010 Issue:10 Volume:104 Page:858-859
ISSN:0340-6245
Container-title:Thrombosis and Haemostasis
language:en
Short-container-title:Thromb Haemost

Author:

Scandellari Raffaella,Vettore Silvia,Scapin Margherita,Bizzaro Nicola,Randi Maria,Fabris Fabrizio

Publisher

Georg Thieme Verlag KG

Subject

Hematology

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH10-01-0041.pdf

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Why thromboembolism occurs in some patients with thrombocytopenia and treatment strategies;Thrombosis Research;2020-12

2. Occurrence of thrombosis in congenital thrombocytopenic disorders;Blood Coagulation & Fibrinolysis;2013-01

3. Transient hemiparesis in a 14-year-old boy with MYH9 disorders;International Journal of Hematology;2012-07-22

4. Short-term eltrombopag for surgical preparation of a patient with inherited thrombocytopenia deriving from MYH9 mutation;Thrombosis and Haemostasis;2012

5. Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May–Hegglin, Sebastian, Fechtner and Epstein syndromes);Journal of Thrombosis and Thrombolysis;2011-08-13

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