Angeborene Skeletterkrankungen
Author:
Publisher
Springer Science and Business Media LLC
Subject
Surgery,Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/article/10.1007/s00112-017-0321-1/fulltext.html
Reference19 articles.
1. Ben Amor IM, Roughley P, Glorieux FH et al (2013) Skeletal clinical characteristics of osteogenesis imperfecta caused by haploinsufficiency mutations in COL1A1. J Bone Miner Res 28:2001–2007
2. Bishop N (2015) Clinical management of hypophosphatasia. Clin Cases Miner Bone Metab 12:170–173
3. Carpenter TO, Imel EA, Ruppe MD et al (2014) Randomized trial of the anti-FGF23 antibody KRN23 in X‑linked hypophosphatemia. J Clin Invest 124:1587–1597
4. Dogba MJ, Rauch F, Wong T et al (2014) From pediatric to adult care: strategic evaluation of a transition program for patients with osteogenesis imperfecta. BMC Health Serv Res 14:489
5. Forlino A, Cabral WA, Barnes AM et al (2011) New perspectives on osteogenesis imperfecta. Nat Rev Endocrinol 7:540–557
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3. Pharmacotherapy in Rare Skeletal Diseases;Handbook of Experimental Pharmacology;2019
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