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Bernward Hinkes

Showing results (1-10 of 14) with videos related to

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Pediatric Nephrology (Berlin, Germany)|April 6, 2012
"Strawberry wees forever?": questionsBernward Hinkes, Kerstin Benz, Julia Köhler, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2008
Cyclosporin A is superior to cyclophosphamide in children with steroid-resistant nephrotic syndrome-a randomized controlled multicentre trial by the Arbeitsgemeinschaft für Pädiatrische NephrologieChristian Plank, Veronica Kalb, Bernward Hinkes, et al.
Pediatric Nephrology (Berlin, Germany)|January 12, 2007
Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndromeRasheed Gbadegesin, Bernward Hinkes, Christopher Vlangos, et al.
Journal of the American Society of Nephrology : JASN|January 25, 2008
Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndromeBernward Hinkes, Christopher Vlangos, Saskia Heeringa, et al.
Acta Neuropathologica|February 1, 2007
Ependymoma gene expression profiles associated with histological subtype, proliferation, and patient survivalInna Lukashova-v Zangen, Susanne Kneitz, Camelia-Maria Monoranu, et al.
Applied Clinical Informatics|August 8, 2019
User-Centered Development of an Online Platform for Drug Dosing Recommendations in PediatricsWolfgang Rödle, Stefan Wimmer, Julia Zahn, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 27, 2008
Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndromeSaskia F Heeringa, Christopher N Vlangos, Gil Chernin, et al.
BMC Nephrology|May 16, 2012
A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathyBernward Hinkes, Karl F Hilgers, Hanno J Bolz, et al.
Plos One|November 26, 2009
A novel TRPC6 mutation that causes childhood FSGSSaskia F Heeringa, Clemens C Möller, Jianyang Du, et al.
Pediatric Blood & Cancer|July 29, 2011
Frequency, risk-factors and survival of children with atypical teratoid rhabdoid tumors (AT/RT) of the CNS diagnosed between 1988 and 2004, and registered to the German HIT databaseKatja von Hoff, Bernward Hinkes, Elke Dannenmann-Stern, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Pediatric Nephrology (Berlin, Germany)|April 6, 2012
"Strawberry wees forever?": questionsBernward Hinkes, Kerstin Benz, Julia Köhler, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2008
Cyclosporin A is superior to cyclophosphamide in children with steroid-resistant nephrotic syndrome-a randomized controlled multicentre trial by the Arbeitsgemeinschaft für Pädiatrische NephrologieChristian Plank, Veronica Kalb, Bernward Hinkes, et al.
Pediatric Nephrology (Berlin, Germany)|January 12, 2007
Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndromeRasheed Gbadegesin, Bernward Hinkes, Christopher Vlangos, et al.
Journal of the American Society of Nephrology : JASN|January 25, 2008
Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndromeBernward Hinkes, Christopher Vlangos, Saskia Heeringa, et al.
Acta Neuropathologica|February 1, 2007
Ependymoma gene expression profiles associated with histological subtype, proliferation, and patient survivalInna Lukashova-v Zangen, Susanne Kneitz, Camelia-Maria Monoranu, et al.
Applied Clinical Informatics|August 8, 2019
User-Centered Development of an Online Platform for Drug Dosing Recommendations in PediatricsWolfgang Rödle, Stefan Wimmer, Julia Zahn, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 27, 2008
Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndromeSaskia F Heeringa, Christopher N Vlangos, Gil Chernin, et al.
BMC Nephrology|May 16, 2012
A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathyBernward Hinkes, Karl F Hilgers, Hanno J Bolz, et al.
Plos One|November 26, 2009
A novel TRPC6 mutation that causes childhood FSGSSaskia F Heeringa, Clemens C Möller, Jianyang Du, et al.
Pediatric Blood & Cancer|July 29, 2011
Frequency, risk-factors and survival of children with atypical teratoid rhabdoid tumors (AT/RT) of the CNS diagnosed between 1988 and 2004, and registered to the German HIT databaseKatja von Hoff, Bernward Hinkes, Elke Dannenmann-Stern, et al.
Pageof 2