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Francesco Scolari

Showing results (51-60 of 156) with videos related to

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Blood Purification|June 7, 2006
The kind of vascular access influences the baseline inflammatory status and epoetin response in chronic hemodialysis patientsEzio Movilli, Giuliano Brunori, Corrado Camerini, et al.
Molecular Genetics and Metabolism Reports|November 8, 2022
α-Gal A missense variants associated with Fabry disease can lead to ER stress and induction of the unfolded protein responseFrancesco Consolato, Maurizio De Fusco, Céline Schaeffer, et al.
Clinical Kidney Journal|October 12, 2018
Patients with primary membranous nephropathy lack auto-antibodies against LDL receptor, the homologue of megalin in human glomeruliMaurizio Bruschi, Giovanni Candiano, Corrado Murtas, et al.
Kidney International Reports|May 2, 2022
Lessons From the Clinic: ADPKD Genetic Test Unraveling Severe Phenotype, Intrafamilial Variability, and New, Rare Causing GenotypeClaudia Izzi, Chiara Dordoni, Elisa Delbarba, et al.
Clinical Journal of the American Society of Nephrology : CJASN|December 19, 2009
Lack of association between dialysis modality and outcomes in atheroembolic renal diseasePietro Ravani, Rossella Gaggi, Cristiana Rollino, et al.
Clinical Kidney Journal|February 26, 2024
Monoallelic pathogenic <i>IFT140</i> variants are a common cause of autosomal dominant polycystic kidney disease-spectrum phenotypeChiara Dordoni, Letizia Zeni, Diego Toso, et al.
Pediatric Nephrology (Berlin, Germany)|March 8, 2011
Alport syndrome and leiomyomatosis: the first deletion extending beyond COL4A6 intron 2Vera Uliana, Elena Marcocci, Mafalda Mucciolo, et al.
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.
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.
Journal of the American Society of Nephrology : JASN|September 29, 2006
Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndromeGiovanni Candiano, Luca Musante, Maurizio Bruschi, et al.
Pageof 16

Showing results (51-60 of 156) with videos related to

Sort By:
Pageof 16
Blood Purification|June 7, 2006
The kind of vascular access influences the baseline inflammatory status and epoetin response in chronic hemodialysis patientsEzio Movilli, Giuliano Brunori, Corrado Camerini, et al.
Molecular Genetics and Metabolism Reports|November 8, 2022
α-Gal A missense variants associated with Fabry disease can lead to ER stress and induction of the unfolded protein responseFrancesco Consolato, Maurizio De Fusco, Céline Schaeffer, et al.
Clinical Kidney Journal|October 12, 2018
Patients with primary membranous nephropathy lack auto-antibodies against LDL receptor, the homologue of megalin in human glomeruliMaurizio Bruschi, Giovanni Candiano, Corrado Murtas, et al.
Kidney International Reports|May 2, 2022
Lessons From the Clinic: ADPKD Genetic Test Unraveling Severe Phenotype, Intrafamilial Variability, and New, Rare Causing GenotypeClaudia Izzi, Chiara Dordoni, Elisa Delbarba, et al.
Clinical Journal of the American Society of Nephrology : CJASN|December 19, 2009
Lack of association between dialysis modality and outcomes in atheroembolic renal diseasePietro Ravani, Rossella Gaggi, Cristiana Rollino, et al.
Clinical Kidney Journal|February 26, 2024
Monoallelic pathogenic <i>IFT140</i> variants are a common cause of autosomal dominant polycystic kidney disease-spectrum phenotypeChiara Dordoni, Letizia Zeni, Diego Toso, et al.
Pediatric Nephrology (Berlin, Germany)|March 8, 2011
Alport syndrome and leiomyomatosis: the first deletion extending beyond COL4A6 intron 2Vera Uliana, Elena Marcocci, Mafalda Mucciolo, et al.
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.
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.
Journal of the American Society of Nephrology : JASN|September 29, 2006
Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndromeGiovanni Candiano, Luca Musante, Maurizio Bruschi, et al.
Pageof 16