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Wiener 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 Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 3, 2013
A nonclassical IFITM5 mutation located in the coding region causes severe osteogenesis imperfecta with prenatal onsetHeike Hoyer-Kuhn, Oliver Semler, Lutz Garbes, 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.Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|October 13, 2018
TBS as a Tool to Differentiate the Impact of Antiresorptives onCortical and Trabecular Bone in Children With OsteogenesisImperfectaMirko Rehberg, Renaud Winzenrieth, Heike Hoyer-Kuhn, et al.Calcified Tissue International|October 5, 2013
Hyperosteoidosis and hypermineralization in the same bone: bone tissue analyses in a boy with a homozygous BMP1 mutationHeike Hoyer-Kuhn, Oliver Semler, Eckhard Schoenau, et al.Pageof 14