CORTELLA, IRENE
CORTELLA, IRENE
Coexistence of multiple gene variants in some patients with erythrocytoses: Multiple gene variants in erythrocytosis
2024 Benetti, Andrea; Bertozzi, Irene; Ceolotto, Giulio; Cortella, Irene; Regazzo, Daniela; Biagetti, Giacomo; Cosi and Maria Luigia Randi, Elisabetta
Correlation between ADAMTS13 activity and neurological impairment in acute thrombotic microangiopathy patients
2016 BERTI DE MARINIS, Giulia; Novello, Stefano; Ferrari, Silvia; Barzon, Isabella; Cortella, Irene; Businaro, MARIA ANTONIETTA; Fabris, Fabrizio; Lombardi, ANNA-MARIA
Relapsing thrombotic thrombocytopenic purpura with low ADAMTS13 antigen levels: An indication for splenectomy?
2019 Lombardi, Anna Maria; Pasquale, Irene Di; Businaro, Maria Antonietta; Cortella, Irene; Fabris, Fabrizio; Vianello, Fabrizio
Spectrum of 5’UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected
2017 Ferrari, Silvia; Lombardi, ANNA-MARIA; Putti, Maria Caterina; Bertomoro, Antonella; Cortella, Irene; Barzon, Isabella; Girolami, Antonio; Fabris, Fabrizio
VLDL-Apo B 100 fractional synthesis rate (FSR) is decreased in type 2 diabetes mellitus patients with diabetic nephropathy and hypertriglyceridaemia: possible defect in VLDL-Apo B 100 removal
2013 Tessari, Paolo; Vettore, Monica; R., Barazzoni; Toffolo, GIANNA MARIA; Cortella, Irene; Manesso, Erica; Gabelli, Carlo; M., Zanetti