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Medicine|October 24, 2014
Cortical metabolic arrangement during olfactory processing: proposal for a 18F FDG PET/CT methodological approachAlessandro Micarelli, Marco Pagani, Agostino Chiaravalloti, et al.Plos One|March 19, 2013
Early and phasic cortical metabolic changes in vestibular neuritis onsetMarco Alessandrini, Marco Pagani, Bianca Napolitano, et al.American Journal of Otolaryngology|January 16, 2013
Intra-parotid facial nerve schwannoma with intra-temporal extension; a case report. Is there a role for stereotactic radiotherapy?Gianluca Ingrosso, Elisabetta Ponti, Daniela di Cristino, et al.Journal of Neurology|August 2, 2014
Cerebellar metabolic involvement and its correlations with clinical parameters in vestibular neuritisMarco Alessandrini, Alessandro Micarelli, Agostino Chiaravalloti, et al.Brain Topography|October 7, 2015
Involvement of Subcortical Brain Structures During Olfactory Stimulation in Multiple Chemical SensitivityMarco Alessandrini, Alessandro Micarelli, Agostino Chiaravalloti, et al.Anales Otorrinolaringologicos Ibero-Americanos|December 3, 2003
A novel method for diagnosing chronic rhinosinusitis based on an electronic noseEhab I Mohamed, Ernesto Bruno, Roland Linder, et al.Biochemical and Biophysical Research Communications|March 17, 2010
Connexin 26 (GJB2) mutations, causing KID Syndrome, are associated with cell death due to calcium gating deregulationAlessandro Terrinoni, Andrea Codispoti, Valeria Serra, et al.International Journal of Molecular Sciences|September 28, 2023
Partial Loss of Function ABCA12 Mutations Generate Reduced Deposition of Glucosyl-Ceramide, Leading to Patchy Ichthyosis and Erythrodermia Resembling Erythrokeratodermia Variabilis et Progressiva (EKVP)Alessandro Terrinoni, Gabriele Sala, Ernesto Bruno, et al.Biochemical and Biophysical Research Communications|March 24, 2010
Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing lossAlessandro Terrinoni, Andrea Codispoti, Valeria Serra, et al.Proceedings of the National Academy of Sciences of the United States of America|April 17, 2013
Role of p63 and the Notch pathway in cochlea development and sensorineural deafnessAlessandro Terrinoni, Valeria Serra, Ernesto Bruno, et al.Pageof 4