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Stuart B Bauer

Showing results (81-90 of 100) with videos related to

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American Journal of Medical Genetics. Part A|September 15, 2021
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tractBixia Zheng, Chunyan Wang, Steve Seltzsam, et al.
Neurourology and Urodynamics|February 19, 2021
Losartan prevents bladder fibrosis and protects renal function in rat with neurogenic paralysis bladderYu L He, Jian G Wen, Qing S Pu, et al.
Urology|December 21, 2002
Overview consensus statementDavid R Staskin, Alan J Wein, Karl Erik Andersson, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 2, 2021
Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tractBixia Zheng, Steve Seltzsam, Chunyan Wang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 25, 2016
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tractStefan Kohl, Jing Chen, Asaf Vivante, et al.
The Journal of Urology|August 18, 2009
Nomograms for predicting annual resolution rate of primary vesicoureteral reflux: results from 2,462 childrenCarlos R Estrada, Carlo C Passerotti, Dionne A Graham, et al.
The Journal of Urology|August 21, 2009
Ultrasound versus computerized tomography for evaluating urolithiasisCarlo Passerotti, Jeanne S Chow, Andres Silva, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)Chen-Han Wilfred Wu, Nina Mann, Makiko Nakayama, et al.
Plos One|January 20, 2018
A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral refluxAmelie T van der Ven, Birgit Kobbe, Stefan Kohl, et al.
Kidney International|June 18, 2004
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneitySongshan Jiang, Jordan Gitlin, Fang-Ming Deng, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics. Part A|September 15, 2021
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tractBixia Zheng, Chunyan Wang, Steve Seltzsam, et al.
Neurourology and Urodynamics|February 19, 2021
Losartan prevents bladder fibrosis and protects renal function in rat with neurogenic paralysis bladderYu L He, Jian G Wen, Qing S Pu, et al.
Urology|December 21, 2002
Overview consensus statementDavid R Staskin, Alan J Wein, Karl Erik Andersson, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 2, 2021
Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tractBixia Zheng, Steve Seltzsam, Chunyan Wang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 25, 2016
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tractStefan Kohl, Jing Chen, Asaf Vivante, et al.
The Journal of Urology|August 18, 2009
Nomograms for predicting annual resolution rate of primary vesicoureteral reflux: results from 2,462 childrenCarlos R Estrada, Carlo C Passerotti, Dionne A Graham, et al.
The Journal of Urology|August 21, 2009
Ultrasound versus computerized tomography for evaluating urolithiasisCarlo Passerotti, Jeanne S Chow, Andres Silva, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)Chen-Han Wilfred Wu, Nina Mann, Makiko Nakayama, et al.
Plos One|January 20, 2018
A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral refluxAmelie T van der Ven, Birgit Kobbe, Stefan Kohl, et al.
Kidney International|June 18, 2004
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneitySongshan Jiang, Jordan Gitlin, Fang-Ming Deng, et al.
Pageof 10