Giovanni Barbon

Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes <i>SDHA</i>, <i>TMEM127</i>, <i>MAX</i>, and <i>SDHAF2</i> for Gene-Informed Prevention

Birke Bausch, Francesca Schiavi, Ying Ni et al. · JAMA Oncology · 2017 · 194 citations · Full text

ARMC5 mutation analysis in patients with primary aldosteronism and bilateral adrenal lesions

Paolo Mulatero, Francesca Schiavi, Tracy Ann Williams et al. · Journal of Human Hypertension · 2015 · 47 citations

Adrenal Gland, Urology, Bilateral Adrenal Lesions +6

Usefulness of the Total Thrombus‐Formation Analysis System (T‐<scp>TAS</scp>) in the diagnosis and characterization of von Willebrand disease

Viviana Daidone, Giovanni Barbon, Maria Grazia Cattini et al. · Haemophilia · 2016 · 22 citations

Novel mutations in the L1CAM gene support the complexity of L1 syndrome

Cinzia Bertolin, Francesca Boaretto, Giovanni Barbon et al. · Journal of the Neurological Sciences · 2010 · 17 citations

Mendelian Disorder, Genetic Disorder, Genetics +10

Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease

Elena Pontara, Paolo Gresele, Maria Grazia Cattini et al. · Blood Coagulation & Fibrinolysis · 2014 · 11 citations

Vasculitis, Genetics, Immunology +20