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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
February 23, 2021
Arterial Hypertension in a 10-Year-Old Girl
Alina Meeser, Bodo B Beck, Martin Dübbers, et al.
Plos One
|
May 22, 2013
Dysregulated autophagy contributes to podocyte damage in Fabry's disease
Max C Liebau, Fabian Braun, Katja Höpker, et al.
Clinical Kidney Journal
|
May 5, 2025
Urinary peptide signature distinguishes autosomal recessive polycystic kidney disease from other causes of chronic kidney disease
Kathrin Burgmaier, Bénédicte Buffin-Meyer, Julie Klein, et al.
Neuropediatrics
|
August 31, 2018
Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech Development
Walid Fazeli, Kerstin Becker, Peter Herkenrath, et al.
Pediatric Nephrology (Berlin, Germany)
|
November 28, 2017
Mycophenolate mofetil following glucocorticoid treatment in Henoch-Schönlein purpura nephritis: the role of early initiation and therapeutic drug monitoring
Agnes Hackl, Jan U Becker, Lisa M Körner, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
January 25, 2013
Conditional loss of kidney microRNAs results in congenital anomalies of the kidney and urinary tract (CAKUT)
Malte P Bartram, Martin Höhne, Claudia Dafinger, et al.
The Journal of Cell Biology
|
May 11, 2011
NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway
Sandra Habbig, Malte P Bartram, Roman U Müller, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 16, 2025
Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet)
Albertien M van Eerde, Ana Teixeira, Flavia Galletti, et al.
Pediatric Nephrology (Berlin, Germany)
|
August 8, 2015
Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencing
Stefanie Weber, Anja K Büscher, Henning Hagmann, et al.
Frontiers in Cell and Developmental Biology
|
December 21, 2023
Differential regulation of MYC expression by <i>PKHD1/Pkhd1</i> in human and mouse kidneys: phenotypic implications for recessive polycystic kidney disease
Naoe Harafuji, Chaozhe Yang, Maoqing Wu, et al.
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of 7
Search research articles
Search
Showing results (31-40 of 67) with videos related to
Sort By:
Page
of 7
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
February 23, 2021
Arterial Hypertension in a 10-Year-Old Girl
Alina Meeser, Bodo B Beck, Martin Dübbers, et al.
Plos One
|
May 22, 2013
Dysregulated autophagy contributes to podocyte damage in Fabry's disease
Max C Liebau, Fabian Braun, Katja Höpker, et al.
Clinical Kidney Journal
|
May 5, 2025
Urinary peptide signature distinguishes autosomal recessive polycystic kidney disease from other causes of chronic kidney disease
Kathrin Burgmaier, Bénédicte Buffin-Meyer, Julie Klein, et al.
Neuropediatrics
|
August 31, 2018
Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech Development
Walid Fazeli, Kerstin Becker, Peter Herkenrath, et al.
Pediatric Nephrology (Berlin, Germany)
|
November 28, 2017
Mycophenolate mofetil following glucocorticoid treatment in Henoch-Schönlein purpura nephritis: the role of early initiation and therapeutic drug monitoring
Agnes Hackl, Jan U Becker, Lisa M Körner, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
January 25, 2013
Conditional loss of kidney microRNAs results in congenital anomalies of the kidney and urinary tract (CAKUT)
Malte P Bartram, Martin Höhne, Claudia Dafinger, et al.
The Journal of Cell Biology
|
May 11, 2011
NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway
Sandra Habbig, Malte P Bartram, Roman U Müller, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 16, 2025
Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet)
Albertien M van Eerde, Ana Teixeira, Flavia Galletti, et al.
Pediatric Nephrology (Berlin, Germany)
|
August 8, 2015
Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencing
Stefanie Weber, Anja K Büscher, Henning Hagmann, et al.
Frontiers in Cell and Developmental Biology
|
December 21, 2023
Differential regulation of MYC expression by <i>PKHD1/Pkhd1</i> in human and mouse kidneys: phenotypic implications for recessive polycystic kidney disease
Naoe Harafuji, Chaozhe Yang, Maoqing Wu, et al.
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of 7