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

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

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J-GLOBAL ID：201202223134711570 Reference number：12A1527467

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

MYH9異常の14歳男児における一過性半側不全麻痺

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Material：
Volume： 96 Issue： 3 Page： 376-379 Publication year： Sep. 2012
JST Material Number： F0888A ISSN： 0925-5710 CODEN： IJHEEY Document type： Article
Article type：原著論文 Country of issue： Germany, Federal Republic of (DEU) Language： ENGLISH (EN)

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Clinical hematology in general , Congenital diseases,deformities in general.

Reference (10)：

KUNISHIMA, S. Advances in the understanding of MYH9 disorders. Curr Opin Hematol. 2010, 17, 405-410
ANTONIO, G. Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian, Fechtner and Epstein syndromes). J Thromb Thrombolysis. 2011, 32, 474-477
HELLER, PG. Unexplained recurrent venous thrombosis in a patient with MYH9-related disease. Platelets. 2006, 17, 274-275
MCDUNN, S. Coronary thrombosis in a patient with May-Hegglin anomaly. Am J Clin Pathol. 1991, 95, 715-718
FABRIS, F. Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia. Thromb Haemost. 2010, 104, 858-859

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