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Pediatric Nephrology (Berlin, Germany)|July 11, 2015
HNF1B-associated clinical phenotypes: the kidney and beyondDetlef Bockenhauer, Graciana JaureguiberryNephron. Physiology|June 21, 2006
Bartter syndromes and other salt-losing tubulopathiesRobert Kleta, Detlef BockenhauerBest Practice & Research. Clinical Endocrinology & Metabolism|May 10, 2016
Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant)Daniel G Bichet, Detlef BockenhauerPediatric Nephrology (Berlin, Germany)|January 25, 2013
The blind kidney: disorders affecting kidneys and eyesIsabelle Russell-Eggitt, Detlef BockenhauerNature Reviews. Nephrology|June 17, 2015
Pathophysiology, diagnosis and management of nephrogenic diabetes insipidusDetlef Bockenhauer, Daniel G BichetPediatric Nephrology (Berlin, Germany)|June 6, 2013
Urinary concentration: different ways to open and close the tapDetlef Bockenhauer, Daniel G BichetBest Practice & Research. Clinical Endocrinology & Metabolism|December 2, 2023
Inherited non-FGF23-mediated phosphaturic disorders: A kidney-centric reviewEmma Walker, Wesley Hayes, Detlef BockenhauerPediatric Nephrology (Berlin, Germany)|June 30, 2026
Chronic hyponatraemia with a reset osmostat: when abnormal is normalHannah Butaye, Lotte Hoskens, Detlef BockenhauerClinical Kidney Journal|October 6, 2017
Potential and pitfalls in the genetic diagnosis of kidney diseasesAnne Kesselheim, Emma Ashton, Detlef BockenhauerPediatric Nephrology (Berlin, Germany)|August 5, 2010
Similar renal outcomes in children with ADPKD diagnosed by screening or presenting with symptomsDjalila Mekahli, Adrian S Woolf, Detlef BockenhauerPageof 20