IZZI, Claudia
IZZI, Claudia
Dipartimento di Medicina Molecolare e Traslazionale
[ADPKD and intracranial aneurysms: indications for screening, follow-up and clinical management]
2021-01-01 Econimo, Laura; Zeni, Letizia; Cortinovis, Roberta; Alberici, Federico; Izzi, Claudia; Scolari, Francesco
[ADPKD: predictors of Renal Disease progression]
2016-01-01 Scolari, Francesco; Dallera, Nadia; Saletti, Arianna; Terlizzi, Vincenzo; Izzi, Claudia
[Clinical diagnosis of Autosomal Dominant Polycystic Kidney Disease]
2016-01-01 Magistroni, R; Izzi, C; Scolari, F.
[Genetics and genetic counseling]
2016-01-01 Izzi, C; Liut, F; Dallera, N; Mazza, C; Magistroni, R; Savoldi, G; Scolari, F.
[Hyperuricemia and Gout]
2016-01-01 Delbarba, Elisa; Terlizzi, Vincenzo; Dallera, Nadia; Izzi, Claudia; Scolari, Francesco
[Molecular diagnosis of ADPKD]
2016-01-01 Scolari, Francesco; Savoldi, Gianfranco; Mazza, Cinzia; Izzi, Claudia
[The complex etiopathogenesis of focal segmental glomerulosclerosis]
2020-01-01 Tedesco, Martina; Delbarba, Elisa; Izzi, Claudia; Scolari, Francesco; Alberici, Federico
A new case report of severe mucopolysaccharidosis type VII: diagnosis, treatment with haematopoietic cell transplantation and prenatal diagnosis in a second pregnancy
2018-01-01 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.
2009-01-01 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
2013-01-01 Prefumo, F; Izzi, C
ADPKD and Heart
2017-01-01 Liut, Francesca; Izzi, Claudia; Dallera, Nadia; Scolari, Francesco
Aggregazione familiare di anomalie congenite del rene e delle vie urinarie in un isolato genetic della provincia di Brescia: Risultati dello studio clinico-epidemiologico e genealogico.
2007-01-01 Izzi, C; Jeannin, G; Viola, B; Prati, E; Foramitti, Marina; Rozzi, M; Sottini, Laura; Turina, Silvia; Venturelli, Chiara; Scolari, Francesco
Alport syndrome and leiomyomatosis: the first deletion extending beyond COL4A6 intron 2
2011-01-01 Uliana, V; Marcocci, E; Mucciolo, M; Meloni, I; Izzi, C; Manno, C; Bruttini, M; Mari, F; Scolari, Francesco; Renieri, A; Salviati, L.
Alström syndrome: a rare and usually ignored cause of hereditary tubulo-interstitial nephritis.
2008-01-01 Izzi, C; Marega, A; Maffei, P; Milan, G; Zulato, E; Scolari, Francesco
Alström Syndrome: A Rare Cause of Hereditary Tubulointerstitial Nephritis Due to Defects in the Primary Cilia.
2007-01-01 C., Izzi; A., Marega; R., Tardanico; Scolari, Francesco
An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes
2020-01-01 Živná, Martina; Kidd, Kendrah; Zaidan, Mohamad; Vyleťal, Petr; Barešová, Veronika; Hodaňová, Kateřina; Sovová, Jana; Hartmannová, Hana; Votruba, Miroslav; Trešlová, Helena; Jedličková, Ivana; Sikora, Jakub; Hůlková, Helena; Robins, Victoria; Hnízda, Aleš; Živný, Jan; Papagregoriou, Gregory; Mesnard, Laurent; Beck, Bodo B; Wenzel, Andrea; Tory, Kálmán; Häeffner, Karsten; Wolf, Matthias T F; Bleyer, Michael E; Sayer, John A; Ong, Albert C M; Balogh, Lídia; Jakubowska, Anna; Łaszkiewicz, Agnieszka; Clissold, Rhian; Shaw-Smith, Charles; Munshi, Raj; Haws, Robert M; Izzi, Claudia; Capelli, Irene; Santostefano, Marisa; Graziano, Claudio; Scolari, Francesco; Sussman, Amy; Trachtman, Howard; Decramer, Stephane; Matignon, Marie; Grimbert, Philippe; Shoemaker, Lawrence R; Stavrou, Christoforos; Abdelwahed, Mayssa; Belghith, Neila; Sinclair, Matthew; Claes, Kathleen; Kopel, Tal; Moe, Sharon; Deltas, Constantinos; Knebelmann, Bertrand; Rampoldi, Luca; Kmoch, Stanislav; Bleyer, Anthony J
Autosomal Dominant tubulointerstitial Kidney Disease with Adult onset due to a novel Renin Mutation Mapping in the Mature protein
2019-01-01 Schaeffer, Céline; Izzi, Claudia; Vettori, Andrea; Pasqualetto, Elena; Cittaro, Davide; Lazarevic, Dejan; Caridi, Gianluca; Gnutti, Barbara; Mazza, Cinzia; Jovine, Luca; Scolari, Francesco; Rampoldi, Luca
Autosomal Dominant Tubulointerstitial Kidney Disease: An Emerging Cause of Genetic CKD
2022-01-01 Econimo, L.; Schaeffer, C.; Zeni, L.; Cortinovis, R.; Alberici, F.; Rampoldi, L.; Scolari, F.; Izzi, C.
Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy.
2003-01-01 Izzi, C.; Barbon, Alessandro; Toliat, M. R.; Heils, A.; Becker, C.; Nurnberg, P.; Sander, T.; Barlati, Sergio
Chromosomal Microarray and Fetal Growth Restriction
2017-01-01 Prefumo, Federico; Fichera, Anna; Fratelli, Nicola; Izzi, Claudia
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| [ADPKD and intracranial aneurysms: indications for screening, follow-up and clinical management] | 1-gen-2021 | Econimo, Laura; Zeni, Letizia; Cortinovis, Roberta; Alberici, Federico; Izzi, Claudia; Scolari, Francesco | |
| [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. | |
| [Hyperuricemia and Gout] | 1-gen-2016 | Delbarba, Elisa; Terlizzi, Vincenzo; Dallera, Nadia; Izzi, Claudia; Scolari, Francesco | |
| [Molecular diagnosis of ADPKD] | 1-gen-2016 | Scolari, Francesco; Savoldi, Gianfranco; Mazza, Cinzia; Izzi, Claudia | |
| [The complex etiopathogenesis of focal segmental glomerulosclerosis] | 1-gen-2020 | Tedesco, Martina; Delbarba, Elisa; Izzi, Claudia; Scolari, Francesco; Alberici, Federico | |
| 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 | |
| Aggregazione familiare di anomalie congenite del rene e delle vie urinarie in un isolato genetic della provincia di Brescia: Risultati dello studio clinico-epidemiologico e genealogico. | 1-gen-2007 | Izzi, C; Jeannin, G; Viola, B; Prati, E; Foramitti, Marina; Rozzi, M; Sottini, Laura; Turina, Silvia; Venturelli, Chiara; 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. | |
| Alström syndrome: a rare and usually ignored cause of hereditary tubulo-interstitial nephritis. | 1-gen-2008 | Izzi, C; Marega, A; Maffei, P; Milan, G; Zulato, E; Scolari, Francesco | |
| Alström Syndrome: A Rare Cause of Hereditary Tubulointerstitial Nephritis Due to Defects in the Primary Cilia. | 1-gen-2007 | C., Izzi; A., Marega; R., Tardanico; Scolari, Francesco | |
| An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes | 1-gen-2020 | Živná, Martina; Kidd, Kendrah; Zaidan, Mohamad; Vyleťal, Petr; Barešová, Veronika; Hodaňová, Kateřina; Sovová, Jana; Hartmannová, Hana; Votruba, Miroslav; Trešlová, Helena; Jedličková, Ivana; Sikora, Jakub; Hůlková, Helena; Robins, Victoria; Hnízda, Aleš; Živný, Jan; Papagregoriou, Gregory; Mesnard, Laurent; Beck, Bodo B; Wenzel, Andrea; Tory, Kálmán; Häeffner, Karsten; Wolf, Matthias T F; Bleyer, Michael E; Sayer, John A; Ong, Albert C M; Balogh, Lídia; Jakubowska, Anna; Łaszkiewicz, Agnieszka; Clissold, Rhian; Shaw-Smith, Charles; Munshi, Raj; Haws, Robert M; Izzi, Claudia; Capelli, Irene; Santostefano, Marisa; Graziano, Claudio; Scolari, Francesco; Sussman, Amy; Trachtman, Howard; Decramer, Stephane; Matignon, Marie; Grimbert, Philippe; Shoemaker, Lawrence R; Stavrou, Christoforos; Abdelwahed, Mayssa; Belghith, Neila; Sinclair, Matthew; Claes, Kathleen; Kopel, Tal; Moe, Sharon; Deltas, Constantinos; Knebelmann, Bertrand; Rampoldi, Luca; Kmoch, Stanislav; Bleyer, Anthony J | |
| Autosomal Dominant tubulointerstitial Kidney Disease with Adult onset due to a novel Renin Mutation Mapping in the Mature protein | 1-gen-2019 | Schaeffer, Céline; Izzi, Claudia; Vettori, Andrea; Pasqualetto, Elena; Cittaro, Davide; Lazarevic, Dejan; Caridi, Gianluca; Gnutti, Barbara; Mazza, Cinzia; Jovine, Luca; Scolari, Francesco; Rampoldi, Luca | |
| Autosomal Dominant Tubulointerstitial Kidney Disease: An Emerging Cause of Genetic CKD | 1-gen-2022 | Econimo, L.; Schaeffer, C.; Zeni, L.; Cortinovis, R.; Alberici, F.; Rampoldi, L.; Scolari, F.; Izzi, C. | |
| Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy. | 1-gen-2003 | Izzi, C.; Barbon, Alessandro; Toliat, M. R.; Heils, A.; Becker, C.; Nurnberg, P.; Sander, T.; Barlati, Sergio | |
| Chromosomal Microarray and Fetal Growth Restriction | 1-gen-2017 | Prefumo, Federico; Fichera, Anna; Fratelli, Nicola; Izzi, Claudia |