Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristicsPaola Bianchi, Andréa Zanella, Elisa Fermo et al.|Haematologica|2011Cited by 183
‘Gardos Channelopathy’: a variant of hereditary Stomatocytosis with complex molecular regulationElisa Fermo, Paola Bianchi, Pascal Hänggi et al.|Scientific Reports|2017Cited by 84
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 PatientsAnna Zaninoni, Paola Bianchi, Elisa Fermo et al.|Frontiers in Physiology|2018Cited by 80
A new variant of phosphoglycerate kinase deficiency (p.I371K) with multiple tissue involvement: Molecular and functional characterizationElisa Fermo, Alberto Zanella, Paola Bianchi et al.|Molecular Genetics and Metabolism|2012Cited by 32
Hereditary Xerocytosis due to Mutations in<i>PIEZO1</i>Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated FamiliesElisa Fermo, Paola Bianchi, Cristina Vercellati et al.|Case Reports in Hematology|2017Cited by 28