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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 7, 2004
Antifibrotic, nephroprotective potential of ACE inhibitor vs AT1 antagonist in a murine model of renal fibrosisOliver Gross, Eckhard Schulze-Lohoff, Marie-Louise Koepke, et al.
Animals : an Open Access Journal From MDPI|October 27, 2023
Stepwise Reduction of Dietary Phosphorus in Diets for Piglets and Fattening Pigs of Different Genetic Origin Housed under Various Station Environments-A RingtestJochen Krieg, Gerhard Stalljohann, Michael Oster, et al.
Kidney International|March 13, 2003
Preemptive ramipril therapy delays renal failure and reduces renal fibrosis in COL4A3-knockout mice with Alport syndromeOliver Gross, Bogdan Beirowski, Marie-Louise Koepke, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 24, 2010
Loss of collagen-receptor DDR1 delays renal fibrosis in hereditary type IV collagen diseaseOliver Gross, Rainer Girgert, Bogdan Beirowski, et al.
Arthritis Research & Therapy|March 6, 2009
High frequency of corticosteroid and immunosuppressive therapy in patients with systemic sclerosis despite limited evidence for efficacyNicolas Hunzelmann, Pia Moinzadeh, Ekkehard Genth, et al.
Pediatric Nephrology (Berlin, Germany)|July 13, 2016
Prospective study on the potential of RAAS blockade to halt renal disease in Alport syndrome patients with heterozygous mutationsJohanna Stock, Johannes Kuenanz, Niklas Glonke, et al.
Kidney International|June 18, 2004
DDR1-deficient mice show localized subepithelial GBM thickening with focal loss of slit diaphragms and proteinuriaOliver Gross, Bogdan Beirowski, Scott J Harvey, et al.
Journal of the American Society of Nephrology : JASN|February 18, 2005
Delayed chemokine receptor 1 blockade prolongs survival in collagen 4A3-deficient mice with Alport diseaseVolha Ninichuk, Oliver Gross, Christoph Reichel, et al.
Journal of the American Society of Nephrology : JASN|September 30, 2003
X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" studyJean Philippe Jais, Bertrand Knebelmann, Iannis Giatras, et al.
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