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Simone Sanna-Cherchi

Showing results (1-10 of 93) with videos related to

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Kidney International|May 31, 2014
Recessive mutations in CAKUT and VACTERL associationRik Westland, Simone Sanna-Cherchi
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 20, 2015
[Genetic Basis of Congenital Anomalies of the Kidney and Urinary Tract]Monica Bodria, Simone Sanna-Cherchi
The Journal of Clinical Investigation|January 3, 2018
Genetic basis of human congenital anomalies of the kidney and urinary tractSimone Sanna-Cherchi, Rik Westland, Gian Marco Ghiggeri, et al.
Pediatric Nephrology (Berlin, Germany)|December 11, 2008
Familial forms of nephrotic syndromeGianluca Caridi, Antonella Trivelli, Simone Sanna-Cherchi, et al.
Human Mutation|December 16, 2017
A noncoding variant in GANAB explains isolated polycystic liver disease (PCLD) in a large familyWhitney Besse, Jungmin Choi, Dina Ahram, et al.
Glomerular Diseases|June 12, 2025
Familial Idiopathic Glomerular Disease due to a Unique Renal-Predominant Phenotype of MYH9-Related Disease: A Case ReportNatasha S Freeman, Kelsie Bogyo, Andrew Beenken, et al.
Journal of Child Neurology|September 22, 2016
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement DisorderCaterina Garone, Juliana Gurgel-Giannetti, Simone Sanna-Cherchi, et al.
Pediatric Nephrology (Berlin, Germany)|March 8, 2011
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohortRosemary Thomas, Simone Sanna-Cherchi, Bradley A Warady, et al.
Clinical Journal of the American Society of Nephrology : CJASN|December 28, 2013
Clinical implications of the solitary functioning kidneyRik Westland, Michiel F Schreuder, Johannes B van Goudoever, et al.
Pediatric Nephrology (Berlin, Germany)|April 18, 2007
Genetic approaches to human renal agenesis/hypoplasia and dysplasiaSimone Sanna-Cherchi, Gianluca Caridi, Patricia L Weng, et al.
Pageof 10

Showing results (1-10 of 93) with videos related to

Sort By:
Pageof 10
Kidney International|May 31, 2014
Recessive mutations in CAKUT and VACTERL associationRik Westland, Simone Sanna-Cherchi
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 20, 2015
[Genetic Basis of Congenital Anomalies of the Kidney and Urinary Tract]Monica Bodria, Simone Sanna-Cherchi
The Journal of Clinical Investigation|January 3, 2018
Genetic basis of human congenital anomalies of the kidney and urinary tractSimone Sanna-Cherchi, Rik Westland, Gian Marco Ghiggeri, et al.
Pediatric Nephrology (Berlin, Germany)|December 11, 2008
Familial forms of nephrotic syndromeGianluca Caridi, Antonella Trivelli, Simone Sanna-Cherchi, et al.
Human Mutation|December 16, 2017
A noncoding variant in GANAB explains isolated polycystic liver disease (PCLD) in a large familyWhitney Besse, Jungmin Choi, Dina Ahram, et al.
Glomerular Diseases|June 12, 2025
Familial Idiopathic Glomerular Disease due to a Unique Renal-Predominant Phenotype of MYH9-Related Disease: A Case ReportNatasha S Freeman, Kelsie Bogyo, Andrew Beenken, et al.
Journal of Child Neurology|September 22, 2016
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement DisorderCaterina Garone, Juliana Gurgel-Giannetti, Simone Sanna-Cherchi, et al.
Pediatric Nephrology (Berlin, Germany)|March 8, 2011
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohortRosemary Thomas, Simone Sanna-Cherchi, Bradley A Warady, et al.
Clinical Journal of the American Society of Nephrology : CJASN|December 28, 2013
Clinical implications of the solitary functioning kidneyRik Westland, Michiel F Schreuder, Johannes B van Goudoever, et al.
Pediatric Nephrology (Berlin, Germany)|April 18, 2007
Genetic approaches to human renal agenesis/hypoplasia and dysplasiaSimone Sanna-Cherchi, Gianluca Caridi, Patricia L Weng, et al.
Pageof 10