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Journal of Rare Diseases (Berlin, Germany)|December 26, 2022
UMOD and you! Explaining a rare disease diagnosisHolly Mabillard, Eric Olinger, John A SayerNutrients|July 11, 2023
Clinical and Functional Assessment of Digenicity in Renal Phosphate WastingFriederike Petzold, Ria Schönauer, Andreas Werner, et al.Biochemical Society Transactions|May 7, 2021
Molecular genetics of renal ciliopathiesMiguel Barroso-Gil, Eric Olinger, John A SayerMetabolism: Clinical and Experimental|February 6, 2008
Phenotype of a patient with a de novo mutation in the hepatocyte nuclear factor 1beta/maturity-onset diabetes of the young type 5 geneChristof Mayer, Yvonne Böttcher, Peter Kovacs, et al.Journal of General Internal Medicine|April 19, 2008
Isolated renal relapse of sarcoidosis under low-dose glucocorticoid therapyChristof Mayer, Angela Müller, Jan Halbritter, et al.BMC Nephrology|September 4, 2019
Retrospective genetic analysis illustrates the spectrum of autosomal Alport syndrome in a case of living-related donor kidney transplantationFriederike Petzold, Anette Bachmann, Carsten Bergmann, et al.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.BMC Medical Genetics|October 14, 2016
Diagnosing FSGS without kidney biopsy - a novel INF2-mutation in a family with ESRD of unknown originJohannes Münch, Maik Grohmann, Tom H Lindner, et al.Kidney International|October 24, 2018
The excretion of uromodulin is modulated by the calcium-sensing receptorNatsuko Tokonami, Eric Olinger, Huguette Debaix, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 13, 2012
Parvalbumin: calcium and magnesium buffering in the distal nephronEric Olinger, Beat Schwaller, Johannes Loffing, et al.Pageof 16