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Bodo B Beck

Showing results (21-30 of 105) with videos related to

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Pediatric Nephrology (Berlin, Germany)|April 21, 2015
Nephrotic syndrome and thrombotic microangiopathy caused by cobalamin C deficiencyJens C Koenig, Frank Rutsch, Clemens Bockmeyer, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 4, 2014
Vitamin B6 in primary hyperoxaluria I: first prospective trial after 40 years of practiceHeike Hoyer-Kuhn, Sina Kohbrok, Ruth Volland, et al.
Kidney & Blood Pressure Research|August 26, 2015
Discordant Clinical Course of Vitamin-D-Hydroxylase (CYP24A1) Associated Hypercalcemia in Two Adult Brothers With NephrocalcinosisTilman Jobst-Schwan, Andrea Pannes, Karl Peter Schlingmann, et al.
Pediatric Nephrology (Berlin, Germany)|February 22, 2017
Successful discontinuation of eculizumab under immunosuppressive therapy in DEAP-HUSAgnes Hackl, Rasmus Ehren, Michael Kirschfink, et al.
Pediatric Nephrology (Berlin, Germany)|February 28, 2012
Enteric hyperoxaluria, recurrent urolithiasis, and systemic oxalosis in patients with Crohn's diseaseRenate Hueppelshaeuser, Gerd E von Unruh, Sandra Habbig, et al.
American Journal of Nephrology|May 2, 2009
Renal allograft calcification -- prevalence and etiology in pediatric patientsSandra Habbig, Bodo B Beck, Markus Feldkötter, et al.
Kidney International|July 3, 2014
Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation typeGiorgia Mandrile, Christiaan S van Woerden, Paola Berchialla, et al.
Pediatric Nephrology (Berlin, Germany)|August 24, 2019
Subclinical myocardial disease in patients with primary hyperoxaluria and preserved left ventricular ejection fraction: a two-dimensional speckle-tracking imaging studyRuth Lagies, Floris E A Udink Ten Cate, Markus Feldkötter, et al.
Pediatric Nephrology (Berlin, Germany)|October 11, 2008
Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)Matthias T F Wolf, Bethan E Hoskins, Bodo B Beck, et al.
American Journal of Medical Genetics. Part A|June 3, 2017
A heritable microduplication encompassing TBL1XR1 causes a genomic sister-disorder for the 3q26.32 microdeletion syndromeVera Riehmer, Florian Erger, Peter Herkenrath, et al.
Pageof 11

Showing results (21-30 of 105) with videos related to

Sort By:
Pageof 11
Pediatric Nephrology (Berlin, Germany)|April 21, 2015
Nephrotic syndrome and thrombotic microangiopathy caused by cobalamin C deficiencyJens C Koenig, Frank Rutsch, Clemens Bockmeyer, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 4, 2014
Vitamin B6 in primary hyperoxaluria I: first prospective trial after 40 years of practiceHeike Hoyer-Kuhn, Sina Kohbrok, Ruth Volland, et al.
Kidney & Blood Pressure Research|August 26, 2015
Discordant Clinical Course of Vitamin-D-Hydroxylase (CYP24A1) Associated Hypercalcemia in Two Adult Brothers With NephrocalcinosisTilman Jobst-Schwan, Andrea Pannes, Karl Peter Schlingmann, et al.
Pediatric Nephrology (Berlin, Germany)|February 22, 2017
Successful discontinuation of eculizumab under immunosuppressive therapy in DEAP-HUSAgnes Hackl, Rasmus Ehren, Michael Kirschfink, et al.
Pediatric Nephrology (Berlin, Germany)|February 28, 2012
Enteric hyperoxaluria, recurrent urolithiasis, and systemic oxalosis in patients with Crohn's diseaseRenate Hueppelshaeuser, Gerd E von Unruh, Sandra Habbig, et al.
American Journal of Nephrology|May 2, 2009
Renal allograft calcification -- prevalence and etiology in pediatric patientsSandra Habbig, Bodo B Beck, Markus Feldkötter, et al.
Kidney International|July 3, 2014
Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation typeGiorgia Mandrile, Christiaan S van Woerden, Paola Berchialla, et al.
Pediatric Nephrology (Berlin, Germany)|August 24, 2019
Subclinical myocardial disease in patients with primary hyperoxaluria and preserved left ventricular ejection fraction: a two-dimensional speckle-tracking imaging studyRuth Lagies, Floris E A Udink Ten Cate, Markus Feldkötter, et al.
Pediatric Nephrology (Berlin, Germany)|October 11, 2008
Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)Matthias T F Wolf, Bethan E Hoskins, Bodo B Beck, et al.
American Journal of Medical Genetics. Part A|June 3, 2017
A heritable microduplication encompassing TBL1XR1 causes a genomic sister-disorder for the 3q26.32 microdeletion syndromeVera Riehmer, Florian Erger, Peter Herkenrath, et al.
Pageof 11