Miniaturized Bio-and Chemical-Sensors for Point-of-Care Monitoring of Chronic Kidney Diseases

Por Antonio Tricoli, Giovanni Neri
Publicado em 2018-03-01

Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome

Por Elisabetta Tabolacci, Federica Palumbo, Veronica Nobile, Giovanni Neri
Publicado em 2016-08-01

Estudio clínico y molecular del síndrome de Noonan.

Por Francisco Cammarata-Scalisi, Giovanni Neri, Maria Grazia Pomponi, Giorgia Mancano, Gloria Da Silva, Andrea Avendaño, María Angelina Lacruz-Rengel, Frances Stock, Angel Sosa
Publicado no Investigación Clínica (2012)

Guideline recommendations for diagnosis and clinical management of Ring14 syndrome—first report of an ad hoc task force

Por Berardo Rinaldi, Alessandro Vaisfeld, Sergio Amarri, Chiara Baldo, Giuseppe Gobbi, Pamela Magini, Erto Melli, Giovanni Neri, Francesca Novara, Tommaso Pippucci, Romana Rizzi, Annarosa Soresina, Laura Zampini, Orsetta Zuffardi, Marco Crimi
Publicado em 2017-04-01

DNA Methylation in the Diagnosis of Monogenic Diseases

Por Flavia Cerrato, Angela Sparago, Francesca Ariani, Fulvia Brugnoletti, Luciano Calzari, Fabio Coppedè, Alessandro De Luca, Cristina Gervasini, Emiliano Giardina, Fiorella Gurrieri, Cristiana Lo Nigro, Giuseppe Merla, Monica Miozzo, Silvia Russo, Eugenio Sangiorgi, Silvia M Sirchia, Gabriella Maria Squeo, Silvia Tabano, Elisabetta Tabolacci, Isabella Torrente, Maurizio Genuardi, Giovanni Neri, Andrea Riccio
Publicado em 2020-03-01