Cristina Vercellati

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 · 181 citations · Full text

Medicine, Hematology, Human Genetics +5

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 · 180 citations

Life Sciences, Genetics, Molecular Genetics +17

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 · 163 citations · Full text

Medicine, Hematology, Pathology +16

‘Gardos Channelopathy’: a variant of hereditary Stomatocytosis with complex molecular regulation

Elisa Fermo, Anna Bogdanova, Polina Petkova‐Kirova et al. · Scientific Reports · 2017 · 84 citations · Full text

Life Sciences, Genetics, Hematology +17

Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients

Anna Zaninoni, Elisa Fermo, Cristina Vercellati et al. · Frontiers in Physiology · 2018 · 79 citations · Full text

Medicine, Biochemistry, Hematology +17