Fcγ-receptor 3B ( FCGR3B ) copy number variations in patients with eosinophilic granulomatosis with polyangiitis von Martorana, Davide, PhD, Bonatti, Francesco, PhD, Alberici, Federico, MD, Gioffredi, Andrea, MD, Reina, Michele, PhD, Urban, Maria L., MD, Maritati, Federica, MD, Adorni, Alessia, PhD, Radice, Antonella, PhD, Pizzolato, Silvia, MD, Gregorini, Gina, MD, Jeannin, Guido, MD, Guida, Giuseppe, MD, PhD, Boita, Monica, PhD, Pesci, Alberto, MD, Moroni, Gabriella, MD, Neri, Tauro M., MD, Sinico, Renato A., MD, Vaglio, Augusto, MD, PhD

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PTPN22 R620W polymorphism in the ANCA-associated vasculitides von MARTORANA, Davide, MARITATI, Federica, FRATICELLI, Paolo, GUIDA, Giuseppe, GREGORINI, Gina, POSSENTI, Stefano, MORONI, Gabriella, LEONI, Antonio, PAVONE, Laura, PESCI, Alberto, SINICO, Renato A, TOMA, Lucafrancesco Di, MALERBA, Giovanni, D'AMICO, Marco, TUMIATI, Bruno, D'IPPOLITO, Raffaele, BUZIO, Carlo, NERI, Tauro M, VAGLIO, Augusto, BONATTI, Francesco, ALBERICI, Federico, OLIVA, Elena, SEBASTIO, Paola, MANENTI, Lucio, BRUGNANO, Rachele, CATANOSO, Maria G

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BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study von Musolino, Antonino, Bella, Maria A, Bortesi, Beatrice, Michiara, Maria, Naldi, Nadia, Zanelli, Paola, Capelletti, Marzia, Pezzuolo, Debora, Camisa, Roberta, Savi, Mario, Neri, Tauro M, Ardizzoni, Andrea

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Cryptic 13q34 and 4q35.2 Deletions in an Italian Family von Riccardi, Federica, Rivolta, Gianna F., Uliana, Vera, Grati, Francesca R., La Starza, Roberta, Marcato, Livia, Di Perna, Caterina, Quintavalle, Gabriele, Garavelli, Livia, Rosato, Simonetta, Sammarelli, Gabriella, Neri, Tauro M., Tagliaferri, Annarita, Martorana, Davide

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HLA–DRB4 as a genetic risk factor for Churg‐Strauss syndrome von Vaglio, Augusto, Martorana, Davide, Maggiore, Umberto, Grasselli, Chiara, Zanetti, Adele, Pesci, Alberto, Garini, Giovanni, Manganelli, Paolo, Bottero, Paolo, Tumiati, Bruno, Sinico, Renato A., Savi, Mario, Buzio, Carlo, Neri, Tauro M.

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Chronic periaortitis and HLA–DRB103: Another clue to an autoimmune origin von Martorana, Davide, Vaglio, Augusto, Greco, Paolo, Zanetti, Adele, Moroni, Gabriella, Salvarani, Carlo, Savi, Mario, Buzio, Carlo, Neri, Tauro M.

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A breast cancer patient from Italy with germline mutations in both the BRCA1 and BRCA2 genes von MUSOLINO, Antonino, NALDI, Nadia, MICHIARA, Maria, BELLA, Maria A, ZANELLI, Paola, BORTESI, Beatrice, CAPELLETTI, Marzia, SAVI, Mario, NERI, Tauro M, ARDIZZONI, Andrea

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Alterations of Type IV Collagen α Chains in Patients with Chronic Acquired Glomerulopathies: mRNA Levels, Protein Expression and Urinary Loss von Sanna-Cherchi, Simone, Carnevali, Maria Luisa, Martorana, Davide, Cravedi, Paolo, Maggiore, Umberto, Alinovi, Rossella, Bovino, Achiropita, Mattei, Silvia, Orlandini, Guido, Gatti, Rita, Savi, Mario, Sado, Yoshikazu, Neri, Tauro M., Allegri, Landino

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Molecular profile and clinical variables in BRCA1-positive breast cancers. A population-based study von Musolino, Antonino, Michiara, Maria, Bella, Maria A, Naldi, Nadia, Zanelli, Paola, Bortesi, Beatrice, Capelletti, Marzia, Soldani, Linda, Camisa, Roberta, Martella, Eugenia, Franciosi, Vittorio, Savi, Mario, Neri, Tauro M, Ardizzoni, Andrea, Cascinu, Stefano

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Fc[gamma]-receptor 3B ( FCGR3B ) copy number variations in patients with eosinophilic granulomatosis with polyangiitis von Martorana, Davide, Bonatti, Francesco, Alberici, Federico, Gioffredi, Andrea, Reina, Michele, Urban, Maria L, Maritati, Federica, Adorni, Alessia, Radice, Antonella, Pizzolato, Silvia, Gregorini, Gina, Jeannin, Guido, Guida, Giuseppe, Boita, Monica, Pesci, Alberto, Moroni, Gabriella, Neri, Tauro M, Sinico, Renato A, Vaglio, Augusto

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Association of HLA-DRB10401 allele with chronic pancreatitis von CAVESTRO, Giulia M, FRULLONI, Luca, NERI, Tauro M, SEGHINI, Pietro, NOUVENNE, Antonio, ZANETTI, Adele, BOVO, Paolo, DI MARIO, Francesco, OKOLICSANYI, Lajos, CAVALLINI, Giorgio

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Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas von Ponti, Giovanni, Losi, Lorena, Martorana, Davide, Priola, Manuela, Boni, Elisa, Pollio, Annamaria, Neri, Tauro Maria, Seidenari, Stefania

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Multiple changes in thyroid function in patients with chronic active HCV hepatitis treated with recombinant interferon-alpha von Roti, Elio, Minelli, Roberta, Giuberti, Tiziana, Marchelli, Silvia, Schianchi, Claudia, Gardini, Eliana, Salvi, Mario, Fiaccadori, Franco, Ugolotti, Giorgio, Neri, Tauro M., Braverman, Lewis E.

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Alterations of Type IV Collagen [alpha] Chains in Patients with Chronic Acquired Glomerulopathies: mRNA Levels, Protein Expression and Urinary Loss von Sanna-Cherchi, Simone, Carnevali, Maria Luisa, Martorana, Davide, Cravedi, Paolo, Maggiore, Umberto, Alinovi, Rossella, Bovino, Achiropita, Mattei, Silvia, Orlandini, Guido, Gatti, Rita, Savi, Mario, Sado, Yoshikazu, Neri, Tauro M, Allegri, Landino

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The contribution of MHC region genes in the genetic predisposition to primary sclerosing cholangitis (PSC) von Cavestro, Giulia M., Neri, Tauro M., Seghini, Pietro, Zanelli, Paola F., Zanetti, Adele, Zuin, Massimo, Podda, Mauro, Bollani, Simona, BianchiPorro, Gabriele, Strazzabosco, Mario, Okolicsanyi, Lajos

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HLA-DRB1 and tumor necrosis factor a but not cystic fibrosis transmembrane conductance regulator genes contribute to the genetic susceptibility of primary sclerosing cholangitis von Cavestro, Giulia M., Seghini, Pletro, Neri, Tauro M., Zanelli, Paola F., Podda, Mauro, Selmi, Carlo, Bianchi-Porro, Gabriele, Floreanl, Anna R., Colombo, Massimo, Rosina, Floriano, Strazzabosco, Mario, Okolicsanyl, Lajos

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Fine specificity of the human T-cell response to the hepatitis B virus preS1 antigen von Ferrari, Carlo, Cavalli, Albertina, Penna, Amalia, Valli, Antonietta, Bertoletti, Antonio, Pedretti, Giovanni, Pilli, Massimo, Vitali, Piero, Neri, Tauro M., Giuberti, Tiziana, Fiaccadori, Franco

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T-cell receptor β-chain gene rearrangement and expression during human thymic ontogenesis von BONATI, A, ZANELLI, P, FERRARI, S, PLEBANI, A, STARCICH, B, SAVI, M, NERI, T. M

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The contribution of MHC region genes and the mutations of the CFTR gene in the genetic predisposition to primary sclerosing cholangitis (PSC) von Cavestro, Giulia M., Neri, Tauro M., Seghini, Pietro, Zanelli, Paola F., Zanetti, Adele, Zuin, Massimo, Selmi, Carlo, Podda, Mauro, Bollani, Simona, Bianchi-Porro, Gabriele, Floreani, Anna Rosa, Colombo, Massimo, Rosina, Floriano, Strazzabosco, Mario, Okolicsanyi, Lajos

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Missense mutations in the COL4A5 gene in patients with X-linked alport syndrome von Neri, Tauro M., Zanelli, Paola, De Palma, Giuseppe, Savi, Mario, Rossetti, Sandro, Turco, Alberto E., Pignatti, Gian Franco, Galli, Lucia, Bruttini, Mirella, Renieri, Alessandra, Mingarelli, Rita, Trivelli, Antonella, Pinciaroli, Angela Rosa, Ragaiolo, Mauro, Rizzoni, Gian Franco, De Marchi, Mario

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