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Handbook of Experimental Pharmacology|June 11, 2020
Pharmacotherapy in Rare Skeletal DiseasesHeike Hoyer-Kuhn, Eckhard SchönauWiener Medizinische Wochenschrift (1946)|June 10, 2015
Osteogenesis imperfecta: pathophysiology and treatmentHeike Hoyer-Kuhn, Christian Netzer, Oliver SemlerOrphanet Journal of Rare Diseases|September 20, 2019
Individualized treatment with denosumab in children with osteogenesis imperfecta - follow up of a trial cohortHeike Hoyer-Kuhn, Mirko Rehberg, Christian Netzer, et al.Orphanet Journal of Rare Diseases|September 27, 2014
Two years' experience with denosumab for children with osteogenesis imperfecta type VIHeike Hoyer-Kuhn, Christian Netzer, Friederike Koerber, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 19, 2016
Children with severe Osteogenesis imperfecta and short stature present on average with normal IGF-I and IGFBP-3 levelsHeike Hoyer-Kuhn, Laura Höbing, Julia Cassens, et al.Pediatric Endocrinology Reviews : PER|January 3, 2018
Correlation of Bone Mineral Density on Quality of Life in Patients with Osteogenesis Imperfecta during Treatment with DenosumabHeike Hoyer-Kuhn, Christina Stark, Jeremy Franklin, et al.Paediatric Drugs|April 4, 2019
Current and Emerging Therapeutic Options for the Management of Rare Skeletal DiseasesOliver Semler, Mirko Rehberg, Nava Mehdiani, et al.JBMR Plus|September 22, 2025
Urinary calcium and bone resorption markers during 3 years of denosumab treatment in pediatric osteogenesis imperfectaStefanie Stasek, Susanna Reincke, Mirko Rehberg, et al.Expert Opinion on Investigational Drugs|November 22, 2012
Hyperoxaluria and systemic oxalosis: an update on current therapy and future directionsBodo B Beck, Heike Hoyer-Kuhn, Heike Göbel, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|December 3, 2017
Growth response to growth hormone treatment in patients with SHOX deficiency can be predicted by the Cologne prediction modelHeike Hoyer-Kuhn, Jeremy Franklin, Christine Jones, et al.Pageof 4