B. Bianchi

Inner ear abnormalities in four patients with dRTA and SNHL: clinical and genetic heterogeneity

M. Genuardi, S. Giglio, M. Mortilla, 2009, Pediatric Nephrology.

Prognostic significance of cyclooxygenase-2 pathway and angiogenesis in head and neck squamous cell carcinoma.

E. Masini, A. Franchi, M. Paglierani, 2002, Human pathology.

RNA‐seq is a valuable complement of conventional diagnostic tools in newly diagnosed AML patients

M. Fumagalli, C. Gambacorti-Passerini, R. Piazza, 2015, American journal of hematology.

Profound hypokalemia and hypochloremic metabolic alkalosis during thiazide therapy in a child with Pendred syndrome.

I. Pela, B. Bianchi, M. Bigozzi, 2008, Clinical nephrology.

MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome

F. Torricelli, U. Menchini, I. Passerini, 2014, Molecular vision.

Identification of autoantibodies against inner ear antigens in a cohort of children with idiopathic sensorineural hearing loss

R. Cimaz, C. Lunardi, A. Puccetti, 2013, Autoimmunity.

The Epidemiology of Moebius Syndrome

Roberta Farci, G. Calzetti, Mara Casalini, 2020 .