S. Ferasin

A Novel Mutation in the Upstream Open Reading Frame of the CDKN1B Gene Causes a MEN4 Phenotype

Gianluca Occhi, Daniela Regazzo, Giampaolo Trivellin et al. · PLoS Genetics · 2013 · 150 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Abnormalities of von Willebrand factor are also part of the prothrombotic state of Cushing??s syndrome

Alessandra Casonato, Elena Pontara, Marco Boscaro et al. · Blood Coagulation & Fibrinolysis · 1999 · 114 citations

Medicine, Hematology, Pathology +17

Performance of salivary cortisol in the diagnosis of Cushing's syndrome, adrenal incidentaloma, and adrenal insufficiency

Filippo Ceccato, Mattia Barbot, Marialuisa Zilio et al. · European Journal of Endocrinology · 2013 · 75 citations · Full text

Medicine, Endocrinology, Circadian Rhythms +16

The R304X mutation of the aryl hydrocarbon receptor interacting protein gene in familial isolated pituitary adenomas: Mutational hot-spot or founder effect?

Gianluca Occhi, Marie‐Lise Jaffrain‐Rea, Giampaolo Trivellin et al. · Journal of Endocrinological Investigation · 2010 · 51 citations

Medicine, Endocrinology, Genetics +17

The Glucose-Dependent Insulinotropic Polypeptide Receptor is Overexpressed Amongst GNAS1 Mutation-Negative Somatotropinomas and Drives Growth Hormone (GH)-Promoter Activity in GH3 Cells

Gianluca Occhi, Marco Losa, Nora Albiger et al. · Journal of Neuroendocrinology · 2011 · 50 citations · Full text

Life Sciences, Biochemistry, Endocrinology +17