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Detlef Bockenhauer

Showing results (61-70 of 233) with videos related to

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Nephron|July 1, 2021
Epidemiology of Distal Renal Tubular Acidosis: A Study Using Linked UK Primary Care and Hospital DataFlorence Bianic, Florent Guelfucci, Ludovic Robin, et al.
BMC Bioinformatics|February 10, 2018
OVAS: an open-source variant analysis suite with inheritance modellingMonika Mozere, Mehmet Tekman, Jameela Kari, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2024
Antenatal presentation and early postnatal treatment of infantile hypercalcemia type 2Marcelien Verjans, An Hindryckx, Karen Rosier, et al.
Archives of Disease in Childhood|October 29, 2020
Hyponatraemia despite isotonic maintenance fluid therapy: a time series intervention studyMilan Chromek, Åsa Jungner, Niclas Rudolfson, et al.
Molecular Genetics & Genomic Medicine|September 22, 2016
Founder mutation in KCNJ10 in Pakistani patients with EAST syndromeOla Abdelhadi, Daniela Iancu, Mehmet Tekman, et al.
Pediatric Nephrology (Berlin, Germany)|July 7, 2010
Renal malformations associated with mutations of developmental genes: messages from the clinicShazia Adalat, Detlef Bockenhauer, Sarah E Ledermann, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 10, 2016
Urea is successful in treating inappropriate antidiuretic hormone secretion in an infantStephanie Dufek, Christine Booth, Adrian Carroll, et al.
Pediatric Radiology|August 7, 2010
Postmortem MRI of bladder agenesisBrendan R Barber, Martin A Weber, Detlef Bockenhauer, et al.
Pediatric Nephrology (Berlin, Germany)|April 16, 2004
The risk of cardiovascular disease in adults who have had childhood nephrotic syndromeBrent Lee Lechner, Detlef Bockenhauer, Sandra Iragorri, et al.
Pediatric Nephrology (Berlin, Germany)|January 12, 2020
Mitochondrial DNA mutations in renal disease: an overviewLarissa P Govers, Hakan R Toka, Ali Hariri, et al.
Pageof 24

Showing results (61-70 of 233) with videos related to

Sort By:
Pageof 24
Nephron|July 1, 2021
Epidemiology of Distal Renal Tubular Acidosis: A Study Using Linked UK Primary Care and Hospital DataFlorence Bianic, Florent Guelfucci, Ludovic Robin, et al.
BMC Bioinformatics|February 10, 2018
OVAS: an open-source variant analysis suite with inheritance modellingMonika Mozere, Mehmet Tekman, Jameela Kari, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2024
Antenatal presentation and early postnatal treatment of infantile hypercalcemia type 2Marcelien Verjans, An Hindryckx, Karen Rosier, et al.
Archives of Disease in Childhood|October 29, 2020
Hyponatraemia despite isotonic maintenance fluid therapy: a time series intervention studyMilan Chromek, Åsa Jungner, Niclas Rudolfson, et al.
Molecular Genetics & Genomic Medicine|September 22, 2016
Founder mutation in KCNJ10 in Pakistani patients with EAST syndromeOla Abdelhadi, Daniela Iancu, Mehmet Tekman, et al.
Pediatric Nephrology (Berlin, Germany)|July 7, 2010
Renal malformations associated with mutations of developmental genes: messages from the clinicShazia Adalat, Detlef Bockenhauer, Sarah E Ledermann, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 10, 2016
Urea is successful in treating inappropriate antidiuretic hormone secretion in an infantStephanie Dufek, Christine Booth, Adrian Carroll, et al.
Pediatric Radiology|August 7, 2010
Postmortem MRI of bladder agenesisBrendan R Barber, Martin A Weber, Detlef Bockenhauer, et al.
Pediatric Nephrology (Berlin, Germany)|April 16, 2004
The risk of cardiovascular disease in adults who have had childhood nephrotic syndromeBrent Lee Lechner, Detlef Bockenhauer, Sandra Iragorri, et al.
Pediatric Nephrology (Berlin, Germany)|January 12, 2020
Mitochondrial DNA mutations in renal disease: an overviewLarissa P Govers, Hakan R Toka, Ali Hariri, et al.
Pageof 24