A case of elevated liver enzymes with MYH9 disorder
Author:
Affiliation:
1. Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine
Publisher
Japan Society of Hepatology
Subject
Hepatology
Link
https://www.jstage.jst.go.jp/article/kanzo/57/9/57_475/_pdf
Reference10 articles.
1. 1) Hennes EM, Zeniya M, Czaja AJ, et al. Simplified criteria for the diagnosis of autoimmune hepatitis. Hepatology 2008; 48 (1): 169-176
2. 3) Kunishima S, Saito H. Advances in the understanding of MYH9 disorders. Curr Opin Hematol 2010; 17 (5): 405-410
3. 4) Seri M, Cusano R, Gangarossa S, et al. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. Nat Genet 2000; 26 (1): 103-105
4. 5) Balduini CL, Pecci A, Savoia A. Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias. Br J Haematol 2011; 154 (2): 161-174
5. 6) Althaus K, Greinacher A. MYH9-related platelet disorders. Semin Thromb Hemost 2009; 35 (2): 189-203
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