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Francesco Scolari

Showing results (31-40 of 156) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 29, 2002
Predialysis versus postdialysis hematocrit evaluation during erythropoietin therapyEzio Movilli, Nicoletta Pertica, Corrado Camerini, et al.
Kidney International|June 6, 2003
Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthoodGianluca Caridi, Roberta Bertelli, Francesco Scolari, et al.
Disease Models & Mechanisms|June 7, 2023
Leader peptide or pro-segment mutants of renin are misrouted to mitochondria in autosomal dominant tubulointerstitial kidney diseaseCéline Schaeffer, Maurizio De Fusco, Elena Pasqualetto, et al.
Antimicrobial Resistance and Infection Control|August 11, 2018
<i>Myroides odoratimimus</i> urinary tract infection in an immunocompromised patient: an emerging multidrug-resistant micro-organismGiovanni Lorenzin, Giorgio Piccinelli, Lucrezia Carlassara, et al.
Vaccines|September 23, 2020
<i>Pneumocystis jirevocii</i> and SARS-CoV-2 Co-Infection: A Common Feature in Transplant Recipients?Maria A De Francesco, Federico Alberici, Nicola Bossini, et al.
Journal of Nephrology|July 2, 2003
Towards the identification of (a) gene(s) for autosomal dominant medullary cystic kidney diseaseFrancesco Scolari, Battista Fabio Viola, Gian Marco Ghiggeri, et al.
Kidney International Reports|December 19, 2022
Autosomal Dominant Tubulointerstitial Kidney Disease: An Emerging Cause of Genetic CKDLaura Econimo, Celine Schaeffer, Letizia Zeni, et al.
Kidney International|March 2, 2011
The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathyClaudia Izzi, Pietro Maffei, Gabriella Milan, et al.
International Journal of Cardiology|November 30, 2010
Low cerebrovascular event rate in subjects with patent foramen ovale and different clinical presentations: results from a prospective non randomized study on a population including patients with and without patent foramen ovale closurePompilio Faggiano, Silvia Frattini, Piergiuseppe Piovesana, et al.
Pediatric Nephrology (Berlin, Germany)|April 14, 2010
Genetic studies of IgA nephropathy: past, present, and futureKrzysztof Kiryluk, Bruce A Julian, Robert J Wyatt, et al.
Pageof 16

Showing results (31-40 of 156) with videos related to

Sort By:
Pageof 16
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 29, 2002
Predialysis versus postdialysis hematocrit evaluation during erythropoietin therapyEzio Movilli, Nicoletta Pertica, Corrado Camerini, et al.
Kidney International|June 6, 2003
Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthoodGianluca Caridi, Roberta Bertelli, Francesco Scolari, et al.
Disease Models & Mechanisms|June 7, 2023
Leader peptide or pro-segment mutants of renin are misrouted to mitochondria in autosomal dominant tubulointerstitial kidney diseaseCéline Schaeffer, Maurizio De Fusco, Elena Pasqualetto, et al.
Antimicrobial Resistance and Infection Control|August 11, 2018
<i>Myroides odoratimimus</i> urinary tract infection in an immunocompromised patient: an emerging multidrug-resistant micro-organismGiovanni Lorenzin, Giorgio Piccinelli, Lucrezia Carlassara, et al.
Vaccines|September 23, 2020
<i>Pneumocystis jirevocii</i> and SARS-CoV-2 Co-Infection: A Common Feature in Transplant Recipients?Maria A De Francesco, Federico Alberici, Nicola Bossini, et al.
Journal of Nephrology|July 2, 2003
Towards the identification of (a) gene(s) for autosomal dominant medullary cystic kidney diseaseFrancesco Scolari, Battista Fabio Viola, Gian Marco Ghiggeri, et al.
Kidney International Reports|December 19, 2022
Autosomal Dominant Tubulointerstitial Kidney Disease: An Emerging Cause of Genetic CKDLaura Econimo, Celine Schaeffer, Letizia Zeni, et al.
Kidney International|March 2, 2011
The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathyClaudia Izzi, Pietro Maffei, Gabriella Milan, et al.
International Journal of Cardiology|November 30, 2010
Low cerebrovascular event rate in subjects with patent foramen ovale and different clinical presentations: results from a prospective non randomized study on a population including patients with and without patent foramen ovale closurePompilio Faggiano, Silvia Frattini, Piergiuseppe Piovesana, et al.
Pediatric Nephrology (Berlin, Germany)|April 14, 2010
Genetic studies of IgA nephropathy: past, present, and futureKrzysztof Kiryluk, Bruce A Julian, Robert J Wyatt, et al.
Pageof 16