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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, 6/2020
Rasmus 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 Images
Darshana 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 adolescents
Empar 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 adolescents
Elke 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 vivo
Falko 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 vivo
Falko 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 syndrome
Lutz 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 barrier
Sybille 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 Registry
Christine 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 Syndrome
Stefanie Weber, Holger Thiele, Sevgi Mir, et al.
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Search research articles
Search
Showing results (81-90 of 98) with videos related to
Sort By:
Page
of 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, 6/2020
Rasmus 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 Images
Darshana 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 adolescents
Empar 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 adolescents
Elke 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 vivo
Falko 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 vivo
Falko 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 syndrome
Lutz 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 barrier
Sybille 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 Registry
Christine 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 Syndrome
Stefanie Weber, Holger Thiele, Sevgi Mir, et al.
Page
of 10