Author/Creator: Barbon, G. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Barbon, G.

1. [PP.07.12] ARMC5 MUTATIONS IN PATIENTS WITH PRIMARY ALDOSTERONISM AND BILATERAL ADRENAL LESIONS. (September 2016)

Authors:: Mulatero, P.; Schiavi, F.; Williams, T.A.; Monticone, S.; Barbon, G.; Opocher, G.; Fallo, F.
Journal:: Journal of hypertension
Issue:: Volume 34:(2016) Supplement 2
Page Start:
Record Type:: Journal Article
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2. 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. Issue 3 (September 2015)

Authors:: Casonato, A.; Cattini, M.G.; Barbon, G.; Daidone, V.; Pontara, E.
Journal:: Thrombosis research
Issue:: Volume 136:Issue 3(2015)
Page Start:: 682
Record Type:: Journal Article
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3. Usefulness of the Total Thrombus‐Formation Analysis System (T‐TAS) in the diagnosis and characterization of von Willebrand disease. (13th June 2016)

Authors:: Daidone, V.; Barbon, G.; Cattini, M. G.; Pontara, E.; Romualdi, C.; Di Pasquale, I.; Hosokawa, K.; Casonato, A.
Journal:: Haemophilia
Issue:: Volume 22:Number 6(2016:Nov.)
Page Start:: 949
Record Type:: Journal Article
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