BARZON, ISABELLA
BARZON, ISABELLA
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Risultati 1 - 5 di 5 (tempo di esecuzione: 0.008 secondi).
A NEW SUSPECTED CAUSE OF ERYTHROCYTOSIS: EPAS1 MUTATIONS ASSOCIATED WITH MUTATIONS IN OTHER GENES
2021 Benetti, Andrea; Biagetti, Giacomo; Bertozzi, Irene; Barzon, Isabella; Ceolotto, Giulio; Randi, MARIA LUIGIA
A novel germ-line mutation of c-mpl gene in a sporadic case of essential thrombocythemia
2017 Lombardi, ANNA-MARIA; Ferrari, Silvia; Barzon, Isabella; Navaglia, Filippo; Fabris, Fabrizio; Vianello, Fabrizio
Clinical effect of CALR allele burden in patients with essential thrombocythemia
2021 Bertozzi, I.; Biagetti, G.; Vezzaro, T.; Barzon, I.; Carraro, M.; Fabris, F.; Randi, M. L.
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
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