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Kidney International|October 2, 2013
Dietary phosphate: the challenges of exploring its role in FGF23 regulationMarta Christov, Harald JüppnerJournal of Pediatric Endocrinology & Metabolism : JPEM|June 23, 2006
Different mutations within or upstream of the GNAS locus cause distinct forms of pseudohypoparathyroidismHarald Jüppner, Murat BastepeThe Journal of Clinical Investigation|November 29, 2012
αKlotho: FGF23 coreceptor and FGF23-regulating hormoneHarald Jüppner, Myles WolfBest Practice & Research. Clinical Endocrinology & Metabolism|November 20, 2018
Phosphate homeostasis disordersMarta Christov, Harald JüppnerCurrent Opinion in Nephrology and Hypertension|May 3, 2024
Rare genetic disorders that impair parathyroid hormone synthesis, secretion, or bioactivity provide insights into the diagnostic utility of different parathyroid hormone assaysJakob Höppner, Harald JüppnerAdvances in Experimental Medicine and Biology|March 8, 2012
FGF23 and syndromes of abnormal renal phosphate handlingClemens Bergwitz, Harald JüppnerSeminars in Nephrology|March 8, 2013
Insights from genetic disorders of phosphate homeostasisMarta Christov, Harald JüppnerReviews in Endocrine & Metabolic Disorders|March 28, 2008
Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulationMurat Bastepe, Harald JüppnerBone|November 24, 2012
Autosomal dominant hypophosphatemic rickets in an 85 year old woman: characterization of her disease from infancy through adulthoodMargaret Seton, Harald JüppnerPageof 49