IZZI, Claudia

IZZI, Claudia  

Dipartimento di Medicina Molecolare e Traslazionale  

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Titolo Data di pubblicazione Autore(i) File
[ADPKD: predictors of Renal Disease progression] 1-gen-2016 Scolari, Francesco; Dallera, Nadia; Saletti, Arianna; Terlizzi, Vincenzo; Izzi, Claudia
[Clinical diagnosis of Autosomal Dominant Polycystic Kidney Disease] 1-gen-2016 Magistroni, R; Izzi, C; Scolari, F.
[Genetics and genetic counseling] 1-gen-2016 Izzi, C; Liut, F; Dallera, N; Mazza, C; Magistroni, R; Savoldi, G; Scolari, F.
[Molecular diagnosis of ADPKD] 1-gen-2016 Scolari, Francesco; Savoldi, Gianfranco; Mazza, Cinzia; Izzi, Claudia
A new case report of severe mucopolysaccharidosis type VII: diagnosis, treatment with haematopoietic cell transplantation and prenatal diagnosis in a second pregnancy 1-gen-2018 Francesca, Furlan; Attilio, Rovelli; Miriam, Rigoldi; Mirella, Filocamo; Barbara, Tappino; Douglas, Friday; Gasperini, Serena; Silvana, Mariani; Izzi, Claudia; Bondioni, Maria Pia; Gellera, Cinzia; Anna, Venerando; Nicoletta, Villa; Maria del Carmen Rodriguez Perez, ; Fabio, Pavan; Andrea Biondi Rossella Parini,
A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13. 1-gen-2009 Weng, Pl; Sanna Cherchi, S; Hensle, T; Shapiro, E; Werzberger, A; Caridi, G; Izzi, C; Konka, A; Reese, Ac; Cheng, R; Werzberger, S; Schlussel, Rn; Burk, Rd; Lee, Jh; Ravazzolo, R; Scolari, Francesco; Ghiggeri, Gm; Glassberg, K; Gharavi, A. G.
Abdominal wall defects 1-gen-2013 Prefumo, F; Izzi, C
ADPKD and Heart 1-gen-2017 Liut, Francesca; Izzi, Claudia; Dallera, Nadia; Scolari, Francesco
Alport syndrome and leiomyomatosis: the first deletion extending beyond COL4A6 intron 2 1-gen-2011 Uliana, V; Marcocci, E; Mucciolo, M; Meloni, I; Izzi, C; Manno, C; Bruttini, M; Mari, F; Scolari, Francesco; Renieri, A; Salviati, L.
Chromosomal Microarray and Fetal Growth Restriction 1-gen-2017 Prefumo, Federico; Fichera, Anna; Fratelli, Nicola; Izzi, Claudia
Clinical Significance of the Cystic Phenotype in Alport Syndrome 1-gen-2024 Zeni, L.; Mescia, F.; Toso, D.; Dordoni, C.; Mazza, C.; Savoldi, G.; Econimo, L.; Cortinovis, R.; Fisogni, S.; Alberici, F.; Scolari, F.; Izzi, C.
Comparative X-ray morphometry of prenatal osteogenesis imperfecta type 2 and thanatophoric dysplasia: a contribution to prenatal differential diagnosis. 1-gen-2017 Bondioni, Mp; Pazzaglia, U; Izzi, C; Di Gaetano, G; Laffranchi, F; Baldi, M; Prefumo, F.
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations 1-gen-2013 Migliore, C; Athanasakis, E; Dahoun, S; Wonkam, A; Lees, M; Calabrese, O; Connell, F; Lynch, Sa; Izzi, C; Pompilii, E; Thakur, S; van Maarle, M; Wilson, Lc; Meroni, G.
Copy number disorders are a Common Cause of Congenital Kidney Malformations 1-gen-2012 Simone Sanna Cherchi, ; Kiryluk, Krzysztof; Burgess, Katelyn E.; Bodria, Monica; Sampson, Matthew G.; Hadley, Dexter; Nees, Shannon N.; Sterken, Roel; Verbitsky, Miguel; Lozanovski, Vladimir J.; Anna Materna Kiryluk, ; Barlassina, Cristina; Corbani, Valentina; Carrea, Alba; Perry, Brittany J.; Somenzi, Danio; Murtas, Corrado; Nadica Ristoska Bojkovska, ; Izzi, Claudia; Bianco, Beatrice; Zaniew, Marcin; Flogelova, Hana; Weng, Patricia L.; Kacak, Nilgun; Giberti, Stefania; Gigante, Maddalena; Arapovic, Adela; Drnasin, Kristina; Caridi, Gianluca; Curioni, Simona; Ammenti, Anita; Ferretti, Stefania; Goj, Vinicio; Jobanputra, Vaidehi; Chung, Wendy; Lifton, Richard P.; Clark, Lorraine N.; Saraga, Marijan; Padmanabhan, Sandosh; Dominiczak, Anna F.; Gesualdo, Loreto; Gucev, Zoran; Allegri, Landino; Anna Latos Bielenska, ; Cusi, Daniele; Scolari, Francesco; Tasics, Velibor; Hakonarson, Hakon; Gian Marco Ghiggeri, ; Gharavi, Ali G.
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux 1-gen-2021 Verbitsky, M; Krithivasan, P; Batourina, E; Khan, A; Graham, Se; Marasà, M; Kim, H; Lim, Ty; Weng, Pl; Sánchez-Rodríguez, E; Mitrotti, A; Ahram, Df; Zanoni, F; Fasel, Da; Westland, R; Sampson, Mg; Zhang, Jy; Bodria, M; Kil, Bh; Shril, S; Gesualdo, L; Torri, F; Scolari, F; Izzi, C; van Wijk, Jae; Saraga, M; Santoro, D; Conti, G; Barton, De; Dobson, Mg; Puri, P; Furth, Sl; Warady, Ba; Pisani, I; Fiaccadori, E; Allegri, L; Degl'Innocenti, Ml; Piaggio, G; Alam, S; Gigante, M; Zaza, G; Esposito, P; Lin, F; Simões-E-Silva, Ac; Brodkiewicz, A; Drozdz, D; Zachwieja, K; Miklaszewska, M; Szczepanska, M; Adamczyk, P; Tkaczyk, M; Tomczyk, D; Sikora, P; Mizerska-Wasiak, M; Krzemien, G; Szmigielska, A; Zaniew, M; Lozanovski, Vj; Gucev, Z; Ionita-Laza, I; Stanaway, Ib; Crosslin, Dr; Wong, Cs; Hildebrandt, F; Barasch, J; Kenny, Ee; Loos, Rjf; Levy, B; Ghiggeri, Gm; Hakonarson, H; Latos-Bieleńska, A; Materna-Kiryluk, A; Darlow, Jm; Tasic, V; Willer, C; Kiryluk, K; Sanna-Cherchi, S; Mendelsohn, Cl; Gharavi, Ag
Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD) 1-gen-2016 Carrera, Paola; Calzavara, Silvia; Magistroni, Riccardo; Den Dunnen, Johan T.; Rigo, Francesca; Stenirri, Stefania; Testa, Francesca; Messa, Piergiorgio; Cerutti, Roberta; Scolari, Francesco; Izzi, Claudia; Edefonti, Alberto; Negrisolo, Susanna; Benetti, Elisa; Alibrandi, Maria Teresa Sciarrone; Manunta, Paolo; Boletta, Alessandra; Ferrari, Maurizio
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens 1-gen-2014 Kiryluk, K; Li, Y; Scolari, Francesco; Sanna Cherchi, S; Choi, M; Verbitsky, M; Fasel, D; Lata, S; Prakash, S; Shapiro, S; Fischman, C; Snyder, Hj; Appel, G; Izzi, C; Viola, Bf; Dallera, N; Del Vecchio, L; Barlassina, C; Salvi, E; Bertinetto, Fe; Amoroso, A; Savoldi, S; Rocchietti, M; Amore, A; Peruzzi, L; Coppo, R; Salvadori, M; Ravani, P; Magistroni, R; Ghiggeri, Gm; Caridi, G; Bodria, M; Lugani, F; Allegri, L; Delsante, M; Maiorana, M; Magnano, A; Frasca, G; Boer, E; Boscutti, G; Ponticelli, C; Mignani, R; Marcantoni, C; Di Landro, D; Santoro, D; Pani, A; Polci, R; Feriozzi, S; Chicca, S; Galliani, M; Gigante, M; Gesualdo, L; Zamboli, P; Battaglia, Gg; Garozzo, M; Maixnerová, D; Tesar, V; Eitner, F; Rauen, T; Floege, J; Kovacs, T; Nagy, J; Mucha, K; Pączek, L; Zaniew, M; Mizerska Wasiak, M; Roszkowska Blaim, M; Pawlaczyk, K; Gale, D; Barratt, J; Thibaudin, L; Berthoux, F; Canaud, G; Boland, A; Metzger, M; Panzer, U; Suzuki, H; Goto, S; Narita, I; Caliskan, Y; Xie, J; Hou, P; Chen, N; Zhang, H; Wyatt, Rj; Novak, J; Julian, Ba; Feehally, J; Stengel, B; Cusi, D; Lifton, Rp; Gharavi, Ag
Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes 1-gen-2019 Mackay, Djg; Bliek, J; Lombardi, Mp; Russo, S; Calzari, L; Guzzetti, S; Izzi, C; Selicorni, A; Melis, D; Temple, K; Maher, E; Brioude, F; Netchine, I; Eggermann, T
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations 1-gen-2017 Sanna-Cherchi, Simone; Khan, Kamal; Westland, Rik; Krithivasan, Priya; Fievet, Lorraine; Rasouly, Hila Milo; Ionita-Laza, Iuliana; Capone, Valentina P.; Fasel, David A.; Kiryluk, Krzysztof; Kamalakaran, Sitharthan; Bodria, Monica; Otto, Edgar A.; Sampson, Matthew G.; Gillies, Christopher E.; Vega-Warner, Virginia; Vukojevic, Katarina; Pediaditakis, Igor; Makar, Gabriel S.; Mitrotti, Adele; Verbitsky, Miguel; Martino, Jeremiah; Liu, Qingxue; Na, Young-Ji; Goj, Vinicio; Ardissino, Gianluigi; Gigante, Maddalena; Gesualdo, Loreto; Janezcko, Magdalena; Zaniew, Marcin; Mendelsohn, Cathy Lee; Shril, Shirlee; Hildebrandt, Friedhelm; van Wijk, Joanna A E; Arapovic, Adela; Saraga, Marijan; Allegri, Landino; Izzi, Claudia; Scolari, Francesco; Tasic, Velibor; Ghiggeri, Gian Marco; Latos-Bielenska, Anna; Kiryluk, Anna-Materna; Mane, Shrikant; Goldstein, David B.; Lifton, Richard P.; Katsanis, Nicholas; Davis, Erica E.; Gharavi, Ali G.
Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literature 1-gen-2018 Agostini, A; Marchetti, D; Izzi, C; Cocco, I; Pinelli, L; Accorsi, P; Iascone Maria, R; Giordano, L