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Pediatric Transplantation
|
April 4, 2017
Dyslipidemia after pediatric renal transplantation-The impact of immunosuppressive regimens
Sandra Habbig, Ruth Volland, Kai Krupka, et al.
Scientific Reports
|
July 18, 2019
Arterial tissue transcriptional profiles associate with tissue remodeling and cardiovascular phenotype in children with end-stage kidney disease
Christian Freise, Betti Schaefer, Maria Bartosova, et al.
Kidney International Reports
|
February 5, 2024
Multicenter Long-Term Real World Data on Treatment With Lumasiran in Patients With Primary Hyperoxaluria Type 1
Cristina Martin-Higueras, Lodovica Borghese, Armando Torres, et al.
European Journal of Human Genetics : EJHG
|
July 12, 2012
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies
Bodo B Beck, Anne Baasner, Anja Buescher, et al.
Kidney International Reports
|
February 23, 2023
Modeling of <i>ACTN4</i>-Based Podocytopathy Using <i>Drosophila</i> Nephrocytes
Johanna Odenthal, Sebastian Dittrich, 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.
Clinical Journal of the American Society of Nephrology : CJASN
|
November 18, 2017
Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies
Jens König, Birgitta Kranz, Sabine König, et al.
Human Molecular Genetics
|
February 19, 2013
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expression
Valeska Frank, Sandra Habbig, Malte P Bartram, et al.
Experimental & Molecular Medicine
|
July 1, 2018
Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalus
Claudia Dafinger, Markus M Rinschen, Lori Borgal, et al.
Plos One
|
August 11, 2017
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia
Beata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 74) with videos related to
Sort By:
Page
of 8
Pediatric Transplantation
|
April 4, 2017
Dyslipidemia after pediatric renal transplantation-The impact of immunosuppressive regimens
Sandra Habbig, Ruth Volland, Kai Krupka, et al.
Scientific Reports
|
July 18, 2019
Arterial tissue transcriptional profiles associate with tissue remodeling and cardiovascular phenotype in children with end-stage kidney disease
Christian Freise, Betti Schaefer, Maria Bartosova, et al.
Kidney International Reports
|
February 5, 2024
Multicenter Long-Term Real World Data on Treatment With Lumasiran in Patients With Primary Hyperoxaluria Type 1
Cristina Martin-Higueras, Lodovica Borghese, Armando Torres, et al.
European Journal of Human Genetics : EJHG
|
July 12, 2012
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies
Bodo B Beck, Anne Baasner, Anja Buescher, et al.
Kidney International Reports
|
February 23, 2023
Modeling of <i>ACTN4</i>-Based Podocytopathy Using <i>Drosophila</i> Nephrocytes
Johanna Odenthal, Sebastian Dittrich, 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.
Clinical Journal of the American Society of Nephrology : CJASN
|
November 18, 2017
Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies
Jens König, Birgitta Kranz, Sabine König, et al.
Human Molecular Genetics
|
February 19, 2013
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expression
Valeska Frank, Sandra Habbig, Malte P Bartram, et al.
Experimental & Molecular Medicine
|
July 1, 2018
Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalus
Claudia Dafinger, Markus M Rinschen, Lori Borgal, et al.
Plos One
|
August 11, 2017
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia
Beata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, et al.
Page
of 8