Giuseppe Loffredo
Naples, Italy
Last Updated: 09/26/2026
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Found 8 publications
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene.
Journal: British journal of haematology
Published: May 04, 2017
Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.
Journal: Haematologica
Published: April 26, 2014
MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.
Journal: Human mutation
Published: June 03, 2013
Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study.
Journal: British journal of haematology
Published: January 05, 2013
Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes.
Journal: Molecular cytogenetics
Published: August 01, 2012
Alteration of liver enzymes is a feature of the MYH9-related disease syndrome.
Journal: PloS one
Published: December 12, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026