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, Anna Bogdanova 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 case of complete adenylate kinase deficiency due to a nonsense mutation in <i>AK‐1</i> gene (Arg 107 → Stop, CGA → TGA) associated with chronic haemolytic anaemiaPaola Bianchi, Alberto Zanella, Fiorenza Barraco et al.|British Journal of Haematology|1999Cited by 34
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