BARBON, GIOVANNI

BARBON, GIOVANNI  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
ARMC5 mutation analysis in patients with primary aldosteronism and bilateral adrenal lesions 2016 SCHIAVI, FRANCESCABARBON, GIOVANNIOPOCHER, GIUSEPPEFALLO, FRANCESCO + JOURNAL OF HUMAN HYPERTENSION - -
Loss of cysteine 584 impairs the storage and release, but not the synthesis of von Willebrand factor 2014 DAIDONE, VIVIANABARBON, GIOVANNIPONTARA, ELENAZAMPESE, ENRICOPIZZO, PAOLACASONATO, SANDRA + THROMBOSIS AND HAEMOSTASIS - -
Severe, recessive type 1 is a discrete form of von Willebrand disease: The lesson learned from the c.1534-3C>A von Willebrand factor mutation 2015 CASONATO, SANDRAPELOSO CATTINI, MARIA GRAZIABARBON, GIOVANNIDAIDONE, VIVIANAPONTARA, ELENA THROMBOSIS RESEARCH - -
Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease. 2014 PONTARA, ELENAGRESELE, PAOLOPELOSO CATTINI, MARIA GRAZIADAIDONE, VIVIANABARBON, GIOVANNIGIROLAMI, ANTONIOZANONATO, ELISACASONATO, SANDRA BLOOD COAGULATION & FIBRINOLYSIS - -
The p.R1819_C1948delinsS mutation makes von Willebrand factor ADAMTS13-resistant and reduces its collagen-binding capacity 2015 DAIDONE, VIVIANASAGA, GIORGIABARBON, GIOVANNIPONTARA, ELENAPELOSO CATTINI, MARIA GRAZIAMORPURGO, MARGHERITAZANOTTI, GIUSEPPECASONATO, SANDRA BRITISH JOURNAL OF HAEMATOLOGY - -
Usefulness of the Total Thrombus-Formation Analysis System (T-TAS) in the diagnosis and characterization of von Willebrand disease 2016 DAIDONE, VIVIANABARBON, GIOVANNIPELOSO CATTINI, MARIA GRAZIAPONTARA, ELENAROMUALDI, CHIARADI PASQUALE, IRENECASONATO, SANDRA + HAEMOPHILIA - -