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Pediatric Nephrology (Berlin, Germany)|October 28, 2017
Prenatal parental decision-making and postnatal outcome in renal oligohydramniosKatrin Mehler, Ingo Gottschalk, Kathrin Burgmaier, et al.
Clinical Nephrology|May 16, 2017
A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndrome
Kathrin Ebner, Nadine Reintjes, Markus Feldkötter, 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.
Pediatric Nephrology (Berlin, Germany)|June 12, 2021
Endurance-oriented training program with children and adolescents on maintenance hemodialysis to enhance dialysis efficacy-DiaSportMarkus Feldkötter, Sarah Thys, Anne Adams, et al.
Clinical Journal of the American Society of Nephrology : CJASN|March 31, 2015
Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1Anja Lehnhardt, Claartje Karnatz, Thurid Ahlenstiel-Grunow, et al.
American Journal of Human Genetics|May 4, 2019
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract ObstructionCaroline M Kolvenbach, Gabriel C Dworschak, Sandra Frese, et al.
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