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Claudia Izzi

Showing results (31-40 of 80) with videos related to

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Kidney International Reports|December 11, 2020
Variable Expressivity of HNF1B Nephropathy, From Renal Cysts and Diabetes to Medullary Sponge Kidney Through Tubulo-interstitial Kidney DiseaseClaudia Izzi, Chiara Dordoni, Laura Econimo, et al.
Scientific Reports|August 14, 2019
Autosomal Dominant Tubulointerstitial Kidney Disease with Adult Onset due to a Novel Renin Mutation Mapping in the Mature ProteinCéline Schaeffer, Claudia Izzi, Andrea Vettori, et al.
Prenatal Diagnosis|June 4, 2019
Prenatal findings in oral-facial-digital syndrome type VI: Report of three cases and literature reviewChiara Dordoni, Federico Prefumo, Maria Iascone, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 2020
Testicular Involvement is a Hallmark of Apo A-I Leu75Pro Mutation AmyloidosisAndrea Delbarba, Paolo Facondo, Simona Fisogni, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 21, 2024
Clinical Significance of the Cystic Phenotype in Alport SyndromeLetizia Zeni, Federica Mescia, Diego Toso, et al.
Journal of the American Society of Nephrology : JASN|October 14, 2005
Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritisGina Gregorini, Claudia Izzi, Laura Obici, et al.
Prenatal Diagnosis|July 28, 2015
Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesisFrancesca Malvestiti, Cristina Agrati, Beatrice Grimi, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosisLucia Micale, Maria Giuseppina Turturo, Carmela Fusco, et al.
American Journal of Medical Genetics. Part A|August 17, 2013
Prenatal presentation and postnatal evolution of a patient with Jansen metaphyseal dysplasia with a novel missense mutation in PTH1RGianfranco Savoldi, Claudia Izzi, Marino Signorelli, et al.
Kidney International Reports|April 20, 2026
Sodium-Glucose Cotransporter-2-inhibitors in Adult Patients With Alport SyndromeDiego Toso, Valeria Cinquina, Laura Econimo, et al.
Pageof 8

Showing results (31-40 of 80) with videos related to

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Pageof 8
Kidney International Reports|December 11, 2020
Variable Expressivity of HNF1B Nephropathy, From Renal Cysts and Diabetes to Medullary Sponge Kidney Through Tubulo-interstitial Kidney DiseaseClaudia Izzi, Chiara Dordoni, Laura Econimo, et al.
Scientific Reports|August 14, 2019
Autosomal Dominant Tubulointerstitial Kidney Disease with Adult Onset due to a Novel Renin Mutation Mapping in the Mature ProteinCéline Schaeffer, Claudia Izzi, Andrea Vettori, et al.
Prenatal Diagnosis|June 4, 2019
Prenatal findings in oral-facial-digital syndrome type VI: Report of three cases and literature reviewChiara Dordoni, Federico Prefumo, Maria Iascone, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 2020
Testicular Involvement is a Hallmark of Apo A-I Leu75Pro Mutation AmyloidosisAndrea Delbarba, Paolo Facondo, Simona Fisogni, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 21, 2024
Clinical Significance of the Cystic Phenotype in Alport SyndromeLetizia Zeni, Federica Mescia, Diego Toso, et al.
Journal of the American Society of Nephrology : JASN|October 14, 2005
Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritisGina Gregorini, Claudia Izzi, Laura Obici, et al.
Prenatal Diagnosis|July 28, 2015
Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesisFrancesca Malvestiti, Cristina Agrati, Beatrice Grimi, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosisLucia Micale, Maria Giuseppina Turturo, Carmela Fusco, et al.
American Journal of Medical Genetics. Part A|August 17, 2013
Prenatal presentation and postnatal evolution of a patient with Jansen metaphyseal dysplasia with a novel missense mutation in PTH1RGianfranco Savoldi, Claudia Izzi, Marino Signorelli, et al.
Kidney International Reports|April 20, 2026
Sodium-Glucose Cotransporter-2-inhibitors in Adult Patients With Alport SyndromeDiego Toso, Valeria Cinquina, Laura Econimo, et al.
Pageof 8