BARZON, ISABELLA

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BARZON, ISABELLA

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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

Titolo	Data di pubblicazione	Autori	Rivista	Serie	Titolo libro
A NEW SUSPECTED CAUSE OF ERYTHROCYTOSIS: EPAS1 MUTATIONS ASSOCIATED WITH MUTATIONS IN OTHER GENES	2021	Andrea BenettiGiacomo BiagettiIrene BertozziIsabella BarzonGiulio CeolottoMaria Luigia Randi + -	-	-	48° Congress of the Italian Society of Hematology Milano, Italy, October 24-27, 2021 ABSTRACT BOOK
A novel germ-line mutation of c-mpl gene in a sporadic case of essential thrombocythemia	2017	LOMBARDI, ANNA-MARIAFERRARI, SILVIABARZON, ISABELLANavaglia, FilippoFABRIS, FABRIZIOVIANELLO, FABRIZIO + -	BLOOD CELLS, MOLECULES, & DISEASES	-	-
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.	ANNALS OF HEMATOLOGY	-	-
Correlation between ADAMTS13 activity and neurological impairment in acute thrombotic microangiopathy patients	2016	BERTI DE MARINIS, GIULIANOVELLO, STEFANOFERRARI, SILVIABARZON, ISABELLACORTELLA, IRENEBUSINARO, MARIA ANTONIETTAFABRIS, FABRIZIOLOMBARDI, ANNA-MARIA	JOURNAL OF THROMBOSIS AND THROMBOLYSIS	-	-
Spectrum of 5’UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected	2017	FERRARI, SILVIALOMBARDI, ANNA-MARIAPutti, Maria CaterinaBERTOMORO, ANTONELLACORTELLA, IRENEBARZON, ISABELLAGIROLAMI, ANTONIOFABRIS, FABRIZIO + -	PLATELETS	-	-