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Detlef Bockenhauer

Showing results (131-140 of 233) with videos related to

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Kidney International Reports|March 20, 2023
Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic PatientsElizabeth R Wan, Daniela Iancu, Emma Ashton, et al.
Kidney International|May 29, 2016
Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorderRhian L Clissold, Charles Shaw-Smith, Peter Turnpenny, et al.
Kidney International Reports|September 14, 2019
ADPedKD: A Global Online Platform on the Management of Children With ADPKDStéphanie De Rechter, Detlef Bockenhauer, Lisa M Guay-Woodford, et al.
Nature Reviews. Nephrology|January 30, 2021
Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working GroupOlivia Boyer, Franz Schaefer, Dieter Haffner, et al.
Physiological Reports|December 27, 2021
Quantification of FAM20A in human milk and identification of calcium metabolism proteinsVaksha Patel, Enriko Klootwijk, Gail Whiting, et al.
Journal of the American Society of Nephrology : JASN|September 24, 2016
Risk Factors for Severe Renal Disease in Bardet-Biedl SyndromeElizabeth Forsythe, Kathryn Sparks, Sunayna Best, et al.
Pediatric Nephrology (Berlin, Germany)|June 7, 2014
Clinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty yearsJameela A Kari, Giovanni Montini, Detlef Bockenhauer, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 23, 2016
Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologiesPeggy Sekula, Yong Li, Horia C Stanescu, et al.
Pediatric Nephrology (Berlin, Germany)|January 10, 2022
Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene StudyRajiv Sinha, Subal Pradhan, Sushmita Banerjee, et al.
Pediatric Nephrology (Berlin, Germany)|October 5, 2021
Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variantMaria Pia Falcone, Kathryn Pritchard-Jones, Jesper Brok, et al.
Pageof 24

Showing results (131-140 of 233) with videos related to

Sort By:
Pageof 24
Kidney International Reports|March 20, 2023
Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic PatientsElizabeth R Wan, Daniela Iancu, Emma Ashton, et al.
Kidney International|May 29, 2016
Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorderRhian L Clissold, Charles Shaw-Smith, Peter Turnpenny, et al.
Kidney International Reports|September 14, 2019
ADPedKD: A Global Online Platform on the Management of Children With ADPKDStéphanie De Rechter, Detlef Bockenhauer, Lisa M Guay-Woodford, et al.
Nature Reviews. Nephrology|January 30, 2021
Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working GroupOlivia Boyer, Franz Schaefer, Dieter Haffner, et al.
Physiological Reports|December 27, 2021
Quantification of FAM20A in human milk and identification of calcium metabolism proteinsVaksha Patel, Enriko Klootwijk, Gail Whiting, et al.
Journal of the American Society of Nephrology : JASN|September 24, 2016
Risk Factors for Severe Renal Disease in Bardet-Biedl SyndromeElizabeth Forsythe, Kathryn Sparks, Sunayna Best, et al.
Pediatric Nephrology (Berlin, Germany)|June 7, 2014
Clinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty yearsJameela A Kari, Giovanni Montini, Detlef Bockenhauer, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 23, 2016
Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologiesPeggy Sekula, Yong Li, Horia C Stanescu, et al.
Pediatric Nephrology (Berlin, Germany)|January 10, 2022
Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene StudyRajiv Sinha, Subal Pradhan, Sushmita Banerjee, et al.
Pediatric Nephrology (Berlin, Germany)|October 5, 2021
Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variantMaria Pia Falcone, Kathryn Pritchard-Jones, Jesper Brok, et al.
Pageof 24