Pharmacogenomics of Drug Response in Type 2 Diabetes: Toward the Definition of Tailored Therapies?

di Pollastro, Carla, Ziviello, Carmela, Costa, Valerio, Ciccodicola, Alfredo
Pubblicato in PPAR Res (2015)

Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes

di Costa, Valerio, Federico, Antonio, Pollastro, Carla, Ziviello, Carmela, Cataldi, Simona, Formisano, Pietro, Ciccodicola, Alfredo
Pubblicato in Int J Mol Sci (2016)

A Homozygous Missense Mutation in the IRBP Gene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa

di den Hollander, Anneke I., McGee, Terri L., Ziviello, Carmela, Banfi, Sandro, Dryja, Thaddeus P., Gonzalez-Fernandez, Federico, Ghosh, Debashis, Berson, Eliot L.
Pubblicazione 2008

New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma

di Costa, Valerio, Esposito, Roberta, Ziviello, Carmela, Sepe, Romina, Bim, Larissa Valdemarin, Cacciola, Nunzio Antonio, Decaussin-Petrucci, Myriam, Pallante, Pierlorenzo, Fusco, Alfredo, Ciccodicola, Alfredo
Pubblicato in Oncotarget (2015)

Molecular epidemiology of Usher syndrome in Italy

di Vozzi, Diego, Aaspõllu, Anu, Athanasakis, Emmanouil, Berto, Anna, Fabretto, Antonella, Licastro, Danilo, Külm, Maigi, Testa, Francesco, Trevisi, Patrizia, Vahter, Marju, Ziviello, Carmela, Martini, Alessandro, Simonelli, Francesca, Banfi, Sandro, Gasparini, Paolo
Pubblicazione 2011

The <it>ADAMTS18 </it>gene is responsible for autosomal recessive early onset severe retinal dystrophy

di Peluso Ivana, Conte Ivan, Testa Francesco, Dharmalingam Gopuraja, Pizzo Mariateresa, Collin Rob WJ, Meola Nicola, Barbato Sara, Mutarelli Margherita, Ziviello Carmela, Barbarulo Anna Maria, Nigro Vincenzo, Melone Mariarosa AB, Simonelli Francesca, Banfi Sandro
Pubblicazione 2013-01-01

The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy

di Peluso, Ivana, Conte, Ivan, Testa, Francesco, Dharmalingam, Gopuraja, Pizzo, Mariateresa, Collin, Rob WJ, Meola, Nicola, Barbato, Sara, Mutarelli, Margherita, Ziviello, Carmela, Barbarulo, Anna Maria, Nigro, Vincenzo, Melone, Mariarosa AB, Simonelli, Francesca, Banfi, Sandro
Pubblicazione 2013

Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures

di Licastro, Danilo, Mutarelli, Margherita, Peluso, Ivana, Neveling, Kornelia, Wieskamp, Nienke, Rispoli, Rossella, Vozzi, Diego, Athanasakis, Emmanouil, D'Eustacchio, Angela, Pizzo, Mariateresa, D'Amico, Francesca, Ziviello, Carmela, Simonelli, Francesca, Fabretto, Antonella, Scheffer, Hans, Gasparini, Paolo, Banfi, Sandro, Nigro, Vincenzo
Pubblicazione 2012

Gene Therapy for Leber's Congenital Amaurosis is Safe and Effective Through 1.5 Years After Vector Administration

di Simonelli, Francesca, Maguire, Albert M, Testa, Francesco, Pierce, Eric A, Mingozzi, Federico, Bennicelli, Jeannette L, Rossi, Settimio, Marshall, Kathleen, Banfi, Sandro, Surace, Enrico M, Sun, Junwei, Redmond, T Michael, Zhu, Xiaosong, Shindler, Kenneth S, Ying, Gui-Shuang, Ziviello, Carmela, Acerra, Carmela, Wright, J Fraser, McDonnell, Jennifer Wellman, High, Katherine A, Bennett, Jean, Auricchio, Alberto
Pubblicazione 2009