Export 4 results:[ Autore] Titolo Tipo Anno
Filtri: Autore è Pecci, Alessandro [Clear All Filters]
Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations. Blood 2010;116(26):5832-7..
MYH9: Structure, functions and role of non-muscle myosin IIA in human disease. Gene 2018;664:152-167..
MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations. Hum Mutat 2014;35(2):236-47..
Alteration of liver enzymes is a feature of the MYH9-related disease syndrome. PLoS One 2012;7(4):e35986..