Elisa Fermo

Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics

Paola Bianchi, Elisa Fermo, Cristina Vercellati et al. · Haematologica · 2011 · 174 citations · Full text

Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the<i>SEC23B</i>gene

Paola Bianchi, Elisa Fermo, Cristina Vercellati et al. · Human Mutation · 2009 · 174 citations

Red Blood Cell, Genetic Disorder, Genetics +13

Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect

Marcello Mariani, Wilma Barcellini, Cristina Vercellati et al. · Haematologica · 2008 · 161 citations · Full text

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study

Rachael F. Grace, Paola Bianchi, Eduard J. van Beers et al. · Blood · 2018 · 161 citations · Full text

<i>RAS</i> Mutations Contribute to Evolution of Chronic Myelomonocytic Leukemia to the Proliferative Variant

Clara Ricci, Elisa Fermo, Stefania Corti et al. · Clinical Cancer Research · 2010 · 136 citations · Full text