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Simone Sanna-Cherchi

Showing results (11-20 of 93) with videos related to

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Frontiers in Immunology|February 9, 2026
Opportunities and challenges in recurrent diffuse podocytopathy post-transplantation: the critical value of the definitionRachel Nuccitelli, Amadea Toutoungis, Elena Martinelli, et al.
Pediatric Nephrology (Berlin, Germany)|December 3, 2013
The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1Anna Materna-Kiryluk, Krzysztof Kiryluk, Katelyn E Burgess, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 26, 2022
Incorporating genetics services into adult kidney disease careKelsie Bogyo, Natalie Vena, Halie May, et al.
Kidney International|November 15, 2021
Multidisciplinary approaches for elucidating genetics and molecular pathogenesis of urinary tract malformationsKamal Khan, Dina F Ahram, Yangfan P Liu, et al.
G3 (Bethesda, Md.)|December 10, 2024
The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination eventChristopher A Simeone, Michelle T McNulty, Yask Gupta, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 19, 2006
Characterization of a large Lebanese family segregating IgA nephropathyHussein H Karnib, Simone Sanna-Cherchi, Pierre A Zalloua, et al.
American Journal of Medical Genetics. Part A|December 25, 2018
Anomalies of the genitourinary tract in children with 22q11.2 deletion syndromeJason P Van Batavia, Terrence B Crowley, Evanette Burrows, et al.
Clinical Therapeutics|November 9, 2004
Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective studyGian Marco Ghiggeri, Paolo Catarsi, Francesco Scolari, et al.
Nature Communications|February 14, 2023
Impact of diet and host genetics on the murine intestinal mycobiomeYask Gupta, Anna Lara Ernst, Artem Vorobyev, et al.
Journal of the American Society of Nephrology : JASN|April 15, 2005
Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindredsSimone Sanna-Cherchi, Adam Reese, Terry Hensle, et al.
Pageof 10

Showing results (11-20 of 93) with videos related to

Sort By:
Pageof 10
Frontiers in Immunology|February 9, 2026
Opportunities and challenges in recurrent diffuse podocytopathy post-transplantation: the critical value of the definitionRachel Nuccitelli, Amadea Toutoungis, Elena Martinelli, et al.
Pediatric Nephrology (Berlin, Germany)|December 3, 2013
The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1Anna Materna-Kiryluk, Krzysztof Kiryluk, Katelyn E Burgess, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 26, 2022
Incorporating genetics services into adult kidney disease careKelsie Bogyo, Natalie Vena, Halie May, et al.
Kidney International|November 15, 2021
Multidisciplinary approaches for elucidating genetics and molecular pathogenesis of urinary tract malformationsKamal Khan, Dina F Ahram, Yangfan P Liu, et al.
G3 (Bethesda, Md.)|December 10, 2024
The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination eventChristopher A Simeone, Michelle T McNulty, Yask Gupta, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 19, 2006
Characterization of a large Lebanese family segregating IgA nephropathyHussein H Karnib, Simone Sanna-Cherchi, Pierre A Zalloua, et al.
American Journal of Medical Genetics. Part A|December 25, 2018
Anomalies of the genitourinary tract in children with 22q11.2 deletion syndromeJason P Van Batavia, Terrence B Crowley, Evanette Burrows, et al.
Clinical Therapeutics|November 9, 2004
Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective studyGian Marco Ghiggeri, Paolo Catarsi, Francesco Scolari, et al.
Nature Communications|February 14, 2023
Impact of diet and host genetics on the murine intestinal mycobiomeYask Gupta, Anna Lara Ernst, Artem Vorobyev, et al.
Journal of the American Society of Nephrology : JASN|April 15, 2005
Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindredsSimone Sanna-Cherchi, Adam Reese, Terry Hensle, et al.
Pageof 10