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Ria Schönauer

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Current Opinion in Nephrology and Hypertension|January 19, 2024
The genetics of cystinuria - an update and critical reevaluationClàudia Abad Baucells, Ria Schönauer, Jan Halbritter
Nutrients|July 11, 2023
Clinical and Functional Assessment of Digenicity in Renal Phosphate WastingFriederike Petzold, Ria Schönauer, Andreas Werner, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|February 3, 2017
Adrenomedullin - new perspectives of a potent peptide hormoneRia Schönauer, Sylvia Els-Heindl, Annette G Beck-Sickinger
Frontiers in Pediatrics|March 23, 2018
Update on Hereditary Kidney Stone Disease and Introduction of a New Clinical Patient Registry in GermanyJan Halbritter, Anna Seidel, Luise Müller, et al.
Clinical Kidney Journal|June 27, 2022
Novel somatic <i>PBX1</i> mosaicism likely masking syndromic CAKUT in an adult with bilateral kidney hypoplasiaFriederike Petzold, Wenjun Jin, Elena Hantmann, et al.
Frontiers in Genetics|June 4, 2019
Deleterious Impact of a Novel <i>CFH</i> Splice Site Variant in Atypical Hemolytic Uremic SyndromeRia Schönauer, Anna Seidel, Maik Grohmann, et al.
Frontiers in Genetics|July 12, 2021
Challenging Disease Ontology by Instances of Atypical <i>PKHD1</i> and <i>PKD1</i> GeneticsJonathan de Fallois, Ria Schönauer, Johannes Münch, et al.
Journal of Medicinal Chemistry|May 12, 2016
Adrenomedullin 2.0: Adjusting Key Levers for Metabolic StabilityRia Schönauer, Sylvia Els-Heindl, Jan-Patrick Fischer, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|January 16, 2016
Fluorescently labeled adrenomedullin allows real-time monitoring of adrenomedullin receptor trafficking in living cellsRia Schönauer, Anette Kaiser, Cathleen Holze, et al.
Genes & Diseases|July 25, 2022
Defective claudin-10 causes a novel variation of HELIX syndrome through compromised tight junction strand assemblySebastian Sewerin, Jörg Piontek, Ria Schönauer, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Current Opinion in Nephrology and Hypertension|January 19, 2024
The genetics of cystinuria - an update and critical reevaluationClàudia Abad Baucells, Ria Schönauer, Jan Halbritter
Nutrients|July 11, 2023
Clinical and Functional Assessment of Digenicity in Renal Phosphate WastingFriederike Petzold, Ria Schönauer, Andreas Werner, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|February 3, 2017
Adrenomedullin - new perspectives of a potent peptide hormoneRia Schönauer, Sylvia Els-Heindl, Annette G Beck-Sickinger
Frontiers in Pediatrics|March 23, 2018
Update on Hereditary Kidney Stone Disease and Introduction of a New Clinical Patient Registry in GermanyJan Halbritter, Anna Seidel, Luise Müller, et al.
Clinical Kidney Journal|June 27, 2022
Novel somatic <i>PBX1</i> mosaicism likely masking syndromic CAKUT in an adult with bilateral kidney hypoplasiaFriederike Petzold, Wenjun Jin, Elena Hantmann, et al.
Frontiers in Genetics|June 4, 2019
Deleterious Impact of a Novel <i>CFH</i> Splice Site Variant in Atypical Hemolytic Uremic SyndromeRia Schönauer, Anna Seidel, Maik Grohmann, et al.
Frontiers in Genetics|July 12, 2021
Challenging Disease Ontology by Instances of Atypical <i>PKHD1</i> and <i>PKD1</i> GeneticsJonathan de Fallois, Ria Schönauer, Johannes Münch, et al.
Journal of Medicinal Chemistry|May 12, 2016
Adrenomedullin 2.0: Adjusting Key Levers for Metabolic StabilityRia Schönauer, Sylvia Els-Heindl, Jan-Patrick Fischer, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|January 16, 2016
Fluorescently labeled adrenomedullin allows real-time monitoring of adrenomedullin receptor trafficking in living cellsRia Schönauer, Anette Kaiser, Cathleen Holze, et al.
Genes & Diseases|July 25, 2022
Defective claudin-10 causes a novel variation of HELIX syndrome through compromised tight junction strand assemblySebastian Sewerin, Jörg Piontek, Ria Schönauer, et al.
Pageof 4