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Journal of Pediatric Endocrinology & Metabolism : JPEM|June 25, 2025
Height velocity in the detection of growth disorders reconsidered: a retrospective analysis of the DONALD studyIbrahim Duran, Maja Zimmermann, Jonathan Buggisch, 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.Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|June 11, 2015
Comparison of DXA Scans and Conventional X-rays for Spine Morphometry and Bone Age Determination in ChildrenHeike Hoyer-Kuhn, Kai Knoop, Oliver Semler, et al.Journal of Musculoskeletal & Neuronal Interactions|March 1, 2026
Development of Muscle Function in Children with Achondroplasia Under Vosoritide Treatment: A Retrospective Single-Centre Observational StudySusanna Reincke, Stefanie Stasek, Shino Junghänel-Welzing, et al.Annals of Clinical Biochemistry|June 29, 2026
Serum Sclerostin Levels in Children with Osteogenesis ImperfectaSusanna Reincke, Mirko Rehberg, Stefanie Stasek, et al.Journal of the Endocrine Society|March 26, 2025
Real-world Outcome of Vosoritide Treatment in Children With Achondroplasia: A 12-month Retrospective Observational StudySusanna Reincke, Oliver Semler, Shino Junghänel-Welzing, et al.Clinical Journal of the American Society of Nephrology : CJASN|January 4, 2014
Vitamin B6 in primary hyperoxaluria I: first prospective trial after 40 years of practiceHeike Hoyer-Kuhn, Sina Kohbrok, Ruth Volland, 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 Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 13, 2020
Bone Microarchitecture Assessed by Trabecular Bone Score Is Independent of Mobility Level or Height in Pediatric Patients with Cerebral PalsyMirko Rehberg, Manuela Azim, Kyriakos Martakis, et al.Pageof 4