A new feature of the MYH9-related syndrome: Chronic transaminase elevation
Author:
Publisher
Wiley
Subject
Hepatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/hep.25913/fullpdf
Reference6 articles.
1. Mutation in MYH9 result in the May-Hegglin anomaly, and Fetchner and Sebastian syndromes. The May Hegglin/Fetchner Syndrome Consortium;Seri;Nat Genet,2000
2. Recent advances in the understanding and management of MYH9 related inherited thrombocytopenia;Balduini;Br J Haem,2011
3. The spectrum of MYH9 associated nephropathy;Bostrom;Clin J Am Soc Nephrol,2010
4. Distinct roles for non muscle myosin II isoforms in mouse hepatic stellate cells;Liu;J Hepatol,2011
5. Alteration of liver enzymes is a feature of the Myh9-related disease syndrome;Pecci;Plos One,2012
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1. Measurement of immature platelet fraction is useful in the differential diagnosis of MYH9 disorders;International Journal of Laboratory Hematology;2023-06-16
2. MYH9 ‐related disease mutations cause abnormal red blood cell morphology through increased myosin‐actin binding at the membrane;American Journal of Hematology;2019-04-17
3. A case of elevated liver enzymes with MYH9 disorder;Kanzo;2016
4. Progress in understanding the diagnosis and molecular genetics of macrothrombocytopenias;British Journal of Haematology;2015-05-05
5. R705H mutation ofMYH9is associated withMYH9-related disease and not only with non-syndromic deafness DFNA17;Clinical Genetics;2014-07-26
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