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Peter F Hoyer

Showing results (81-90 of 98) with videos related to

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Pediatric Nephrology (Berlin, Germany)|June 6, 2021
Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy -short version of the updated German best practice guideline (S2e) - AWMF register no. 166-001, 6/2020Rasmus Ehren, Marcus R Benz, Paul T Brinkkötter, et al.
Journal of the American Society of Nephrology : JASN|September 4, 2021
PodoSighter: A Cloud-Based Tool for Label-Free Podocyte Detection in Kidney Whole-Slide ImagesDarshana Govind, Jan U Becker, Jeffrey Miecznikowski, et al.
Frontiers in Pediatrics|May 4, 2023
Joint statement for assessing and managing high blood pressure in children and adolescents: Chapter 1. How to correctly measure blood pressure in children and adolescentsEmpar Lurbe, Giuseppe Mancia, Javier Calpe, et al.
Frontiers in Pediatrics|May 1, 2023
Joint statement for assessing and managing high blood pressure in children and adolescents: Chapter 2. How to manage high blood pressure in children and adolescentsElke Wühl, Javier Calpe, Dorota Drożdż, et al.
Scientific Reports|April 14, 2018
Author Correction: Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivoFalko M Heinemann, Peter T Jindra, Clemens L Bockmeyer, et al.
Scientific Reports|November 8, 2017
Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivoFalko M Heinemann, Peter T Jindra, Clemens L Bockmeyer, et al.
Pediatric Transplantation|December 30, 2020
Clinical practice recommendations for recurrence of focal and segmental glomerulosclerosis/steroid-resistant nephrotic syndromeLutz T Weber, Burkhard Tönshoff, Ryszard Grenda, et al.
Kidney International|December 20, 2021
Scaffold polarity proteins Par3A and Par3B share redundant functions while Par3B acts independent of atypical protein kinase C/Par6 in podocytes to maintain the kidney filtration barrierSybille Koehler, Johanna Odenthal, Vivian Ludwig, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2019
HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood RegistryChristine Okorn, Anne Goertz, Udo Vester, et al.
American Journal of Human Genetics|November 15, 2011
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like SyndromeStefanie Weber, Holger Thiele, Sevgi Mir, et al.
Pageof 10

Showing results (81-90 of 98) with videos related to

Sort By:
Pageof 10
Pediatric Nephrology (Berlin, Germany)|June 6, 2021
Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy -short version of the updated German best practice guideline (S2e) - AWMF register no. 166-001, 6/2020Rasmus Ehren, Marcus R Benz, Paul T Brinkkötter, et al.
Journal of the American Society of Nephrology : JASN|September 4, 2021
PodoSighter: A Cloud-Based Tool for Label-Free Podocyte Detection in Kidney Whole-Slide ImagesDarshana Govind, Jan U Becker, Jeffrey Miecznikowski, et al.
Frontiers in Pediatrics|May 4, 2023
Joint statement for assessing and managing high blood pressure in children and adolescents: Chapter 1. How to correctly measure blood pressure in children and adolescentsEmpar Lurbe, Giuseppe Mancia, Javier Calpe, et al.
Frontiers in Pediatrics|May 1, 2023
Joint statement for assessing and managing high blood pressure in children and adolescents: Chapter 2. How to manage high blood pressure in children and adolescentsElke Wühl, Javier Calpe, Dorota Drożdż, et al.
Scientific Reports|April 14, 2018
Author Correction: Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivoFalko M Heinemann, Peter T Jindra, Clemens L Bockmeyer, et al.
Scientific Reports|November 8, 2017
Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivoFalko M Heinemann, Peter T Jindra, Clemens L Bockmeyer, et al.
Pediatric Transplantation|December 30, 2020
Clinical practice recommendations for recurrence of focal and segmental glomerulosclerosis/steroid-resistant nephrotic syndromeLutz T Weber, Burkhard Tönshoff, Ryszard Grenda, et al.
Kidney International|December 20, 2021
Scaffold polarity proteins Par3A and Par3B share redundant functions while Par3B acts independent of atypical protein kinase C/Par6 in podocytes to maintain the kidney filtration barrierSybille Koehler, Johanna Odenthal, Vivian Ludwig, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2019
HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood RegistryChristine Okorn, Anne Goertz, Udo Vester, et al.
American Journal of Human Genetics|November 15, 2011
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like SyndromeStefanie Weber, Holger Thiele, Sevgi Mir, et al.
Pageof 10