Ausgabe 3/2011
Inhalt (10 Artikel)
VDR Haploinsufficiency Impacts Body Composition and Skeletal Acquisition in a Gender-Specific Manner
Francisco J. A. de Paula, Ingrid Dick-de-Paula, Sheila Bornstein, Bahman Rostama, Phuong Le, Sutada Lotinun, Roland Baron, Clifford J. Rosen
Incisor Enamel Formation is Impaired in Transgenic Rats Overexpressing the Type III NaPi Transporter Slc20a1
Hirotaka Yoshioka, Yuji Yoshiko, Tomoko Minamizaki, Sayaka Suzuki, Yoshiro Koma, Asako Nobukiyo, Yusuke Sotomaru, Atsushi Suzuki, Mitsuyasu Itoh, Norihiko Maeda
Do Both Areal BMD and Injurious Falls Explain the Higher Incidence of Fractures in Women than in Men?
Peter Nordström, Fredrik Eklund, Ulf Björnstig, Anna Nordström, Ronny Lorentzon, Harri Sievänen, Yngve Gustafson
The Oncofetal Gene Survivin Promotes Cell Proliferation and Survival in Primary Human Osteoblastic Cells
Philipp Lechler, Jens Schaumburger, Franz X. Köck, Sanjeevi Balakrishnan, Stavros Doukas, Lukas Prantl, Joachim Grifka
MKP-1 Knockout Does not Prevent Glucocorticoid-Induced Bone Disease in Mice
Maria M. Conradie, Andrew C. B. Cato, William F. Ferris, Heidi de Wet, Kay Horsch, Stephen Hough
Bone Mineral Density in Young Women on Methadone Substitution
Gabriella Milos, Luigi M. Gallo, Branca Sosic, Daniel Uebelhart, Gerhard Goerres, Hans-Jörg Haeuselmann, Dominique Eich
Gastrointestinal Tolerability and Patterns of Switching in Patients Treated for Primary Osteoporosis: The Swedish Adherence Register Analysis (SARA)
Erik Landfeldt, Andrea Lang, Sean Robbins, Oskar Ström
Can 11β-Hydroxysteroid Dehydrogenase Activity Predict the Sensitivity of Bone to Therapeutic Glucocorticoids in Inflammatory Bowel Disease?
Mark S. Cooper, Hashir Kriel, Adrian Sayers, William D. Fraser, Amanda M. Williams, Paul M. Stewart, Chris S. Probert, Jonathan H. Tobias
Metabolic Changes Following 500 μg Monthly Administration of Calcidiol: A Study in Normal Females
Stefania Russo, Luciano Carlucci, Cristiana Cipriani, Alessandro Ragno, Sara Piemonte, Romano Del Fiacco, Jessica Pepe, Valeria Fassino, Serena Arima, Elisabetta Romagnoli, Salvatore Minisola
Familial Paget Disease and SQSTM1 Mutations in New Zealand
Tim Cundy, Dorit Naot, Usha Bava, David Musson, Pak Cheung Tong, Mark Bolland