Transient hemiparesis in a 14-year-old boy with MYH9 disorders-Reference-Cited by-同舟云学术

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Transient hemiparesis in a 14-year-old boy with MYH9 disorders

Published:2012-07-22 Issue:3 Volume:96 Page:376-379
ISSN:0925-5710
Container-title:International Journal of Hematology
language:en
Short-container-title:Int J Hematol

Author:

Kitamura Katsumasa,Kunishima Shinji,Tahara Mayu,Ogiwara Shigetoshi,Dobata Nana,Dobata Tomoyuki,Sugihara Akemi,Nakashima Taiji,Sasaki Yasushi,Nagumo Kiyoshi,Kubota Mitsuru,Kinugawa Yoshikazu,Ieko Masahiro,Kumaki Satoru

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Link

http://link.springer.com/content/pdf/10.1007/s12185-012-1149-z.pdf

Reference10 articles.

1. Kunishima S, Saito H. Advances in the understanding of MYH9 disorders. Curr Opin Hematol. 2010;17:405–10.

2. Antonio G, Silvia V, Emanuela B, Fabrizio F. Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian, Fechtner and Epstein syndromes). J Thromb Thrombolysis. 2011;32:474–7.

3. Heller PG, Pecci A, Glembotsky AC, Savoia A, Negro FD, Balduini CL, et al. Unexplained recurrent venous thrombosis in a patient with MYH9-related disease. Platelets. 2006;17:274–5.

4. McDunn S, Hartz W Jr, Ts’Ao C, Green D. Coronary thrombosis in a patient with May-Hegglin anomaly. Am J Clin Pathol. 1991;95:715–8.

5. Fabris F, Scandellari R, Vettore S, Scapin M, Bizzaro N, Randi ML. Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia. Thromb Haemost. 2010;104:858–9.

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