Publications by authors named "Giovanni Barbon"

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Acquired von Willebrand Syndrome Hiding Inherited von Willebrand Disease Can Explain Severe Bleeding in Patients With Aortic Stenosis.
Alessandra Casonato, Eva Galletta, Giuseppe Cella, Giovanni Barbon, Viviana Daidone

Arterioscler Thromb Vasc Biol· September 2020

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Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention.
Birke Bausch, Francesca Schiavi, Ying Ni, Jenny Welander, Attila Patocs, Giovanni Barbon

JAMA Oncol· September 2017

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The p.R1819_C1948delinsS mutation makes von Willebrand factor ADAMTS13-resistant and reduces its collagen-binding capacity.
Viviana Daidone, Giorgia Saga, Giovanni Barbon, Elena Pontara, Maria G Cattini

Br J Haematol· August 2015

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Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease.
Elena Pontara, Paolo Gresele, Maria Grazia Cattini, Viviana Daidone, Giovanni Barbon

Blood Coagul Fibrinolysis· June 2014

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A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy.
Alessandra Casonato, Viviana Daidone, Giovanni Barbon, Elena Pontara, Irene Di Pasquale

Haematologica· January 2013

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The homozygous ganglioside-induced differentiation-associated protein 1 mutation c.373C > T causes a very early-onset neuropathy: case report and literature review.
Carlo Fusco, Valentina Ucchino, Giovanni Barbon, Elena Bonini, Maria Luisa Mostacciuolo

J Child Neurol· January 2011

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Novel mutations in the L1CAM gene support the complexity of L1 syndrome.
Cinzia Bertolin, Francesca Boaretto, Giovanni Barbon, Leonardo Salviati, Elisabetta Lapi

J Neurol Sci· July 2010

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