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Michaela Geßner

Showing results (1-10 of 7) with videos related to

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Plos One|August 14, 2013
Kidney stones in primary hyperoxaluria: new lessons learntDorrit E Jacob, Bernd Grohe, Michaela Geßner, et al.
Frontiers in Genetics|June 14, 2021
Renal and Skeletal Anomalies in a Cohort of Individuals With Clinically Presumed Hereditary Nephropathy Analyzed by Molecular Genetic TestingMichaela Stippel, Korbinian M Riedhammer, Bärbel Lange-Sperandio, et al.
Kidney International|June 15, 2026
Real-world outcomes of pegcetacoplan treatment in C3 glomerulopathy and immune-complex membranoproliferative glomerulonephritisGiulia Bassanese, Ariel Martje Weingarten, Maria Cristina Mancuso, et al.
Kidney International Reports|April 14, 2025
Trio Exome Sequencing in VACTERL AssociationJasmina Ćomić, Erik Tilch, Korbinian M Riedhammer, et al.
Kidney International|February 16, 2024
An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH)Zewu Zhu, Bryan Bo-Ran Ho, Alyssa Chen, et al.
The Journal of Pediatrics|May 14, 2018
Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney DiseaseKathrin Burgmaier, Kevin Kunzmann, Gema Ariceta, et al.
Clinical Genetics|May 26, 2022
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorderMaria B Christensen, Amanda M Levy, Nazanin A Mohammadi, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Plos One|August 14, 2013
Kidney stones in primary hyperoxaluria: new lessons learntDorrit E Jacob, Bernd Grohe, Michaela Geßner, et al.
Frontiers in Genetics|June 14, 2021
Renal and Skeletal Anomalies in a Cohort of Individuals With Clinically Presumed Hereditary Nephropathy Analyzed by Molecular Genetic TestingMichaela Stippel, Korbinian M Riedhammer, Bärbel Lange-Sperandio, et al.
Kidney International|June 15, 2026
Real-world outcomes of pegcetacoplan treatment in C3 glomerulopathy and immune-complex membranoproliferative glomerulonephritisGiulia Bassanese, Ariel Martje Weingarten, Maria Cristina Mancuso, et al.
Kidney International Reports|April 14, 2025
Trio Exome Sequencing in VACTERL AssociationJasmina Ćomić, Erik Tilch, Korbinian M Riedhammer, et al.
Kidney International|February 16, 2024
An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH)Zewu Zhu, Bryan Bo-Ran Ho, Alyssa Chen, et al.
The Journal of Pediatrics|May 14, 2018
Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney DiseaseKathrin Burgmaier, Kevin Kunzmann, Gema Ariceta, et al.
Clinical Genetics|May 26, 2022
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorderMaria B Christensen, Amanda M Levy, Nazanin A Mohammadi, et al.
Pageof 1