Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus

Por De Bonis, Patrizia, Laborante, Antonio, Pizzicoli, Costantina, Stallone, Raffaella, Barbano, Raffaela, Longo, Costanza, Mazzilli, Emilio, Zelante, Leopoldo, Bisceglia, Luigi
Publicado em 2011

Identification and Clinical Characterization of Adult Patients with Multigenerational Diabetes Mellitus

Por Ludovico, Ornella, Carella, Massimo, Bisceglia, Luigi, Basile, Giorgio, Mastroianno, Sandra, Palena, Antonio, De Cosmo, Salvatore, Copetti, Massimiliano, Prudente, Sabrina, Trischitta, Vincenzo
Publicado no PLoS One (2015)

Clinical utility gene card for: Cystinuria

Por Eggermann, Thomas, Zerres, Klaus, Nunes, Virginia, Font-Llitjós, Mariona, Bisceglia, Luigi, Chatzikyriakidou, Anthoula, Strologo, Luca dello, Pras, Elon, Creemers, John, Palacin, Manuel
Publicado em 2012

MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

Por Melchionda, Salvatore, Ahituv, Nadav, Bisceglia, Luigi, Sobe, Tama, Glaser, Fabian, Rabionet, Raquel, Arbones, Maria Lourdes, Notarangelo, Angelo, Di Iorio, Enzo, Carella, Massimo, Zelante, Leopoldo, Estivill, Xavier, Avraham, Karen B., Gasparini, Paolo
Publicado em 2001

Molecular Genetics of Cystinuria: Identification of Four New Mutations and Seven Polymorphisms, and Evidence for Genetic Heterogeneity

Por Gasparini, Paolo, Calonge, Maria Julia, Bisceglia, Luigi, Purroy, Jesus, Dianzani, Irma, Notarangelo, Angelo, Rousaud, Ferran, Gallucci, Michele, Testar, Xavier, Ponzone, Alberto, Estivill, Xavier, Zorzano, Antonio, Palacin, Manuel, Nunes, Virginia, Zelante, Leopoldo
Publicado em 1995

A new locus on 3p23–p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H

Por Bisceglia, Luigi, Zoccolella, Stefano, Torraco, Alessandra, Piemontese, Maria Rosaria, Dell'Aglio, Rosa, Amati, Angela, De Bonis, Patrizia, Artuso, Lucia, Copetti, Massimiliano, Santorelli, Filippo Maria, Serlenga, Luigi, Zelante, Leopoldo, Bertini, Enrico, Petruzzella, Vittoria
Publicado em 2010

The IgA nephropathy Biobank. An important starting point for the genetic dissection of a complex trait

Por Schena, Francesco P, Cerullo, Giuseppina, Torres, Diletta D, Scolari, Francesco, Foramitti, Marina, Amoroso, Antonio, Pirulli, Doroti, Floege, Jürgen, Mertens, Peter R, Zerres, Klaus, Alexopoulos, Efstathios, Kirmizis, Dimitrios, Zelante, Leopoldo, Bisceglia, Luigi, Ghiggeri, Gian M, Frascà, Giovanni M
Publicado em 2005

Genetic Heterogeneity in Italian Families with IgA Nephropathy: Suggestive Linkage for Two Novel IgA Nephropathy Loci

Por Bisceglia, Luigi , Cerullo, Giuseppina , Forabosco, Paola , Torres, Diletta Domenica , Scolari, Francesco , Di Perna, Michele , Foramitti, Marina , Amoroso, Antonio , Bertok, Sara , Floege, Jürgen , Mertens, Peter Rene , Zerres, Klaus , Alexopoulos, Efstathios , Kirmizis, Dimitrios , Ermelinda, Mazzucco , Zelante, Leopoldo , Schena, Francesco Paolo 
Publicado em 2006