Featured Articles
- Barnes A. M., Carter, E. M., Cabral, W. A., Weis, M., Chang, W., Makareeva, E., et al. (2010). Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding. New England Journal of Medicine, 363(1), 521–528. PMID: 20089953
- Forlino, A., Cabral, W. A., Barnes, A. M., & Marini, J. C. (2011). New perspectives on osteogenesis imperfecta. Nature Reviews Endocrinology, 7, 540–557. PMID: 21670757
- Gentry B. A., Ferreira, J. A., McCambridge, A. J., Brown, M., & Phillips, C. L. (2010). Skeletal muscle weakness in osteogenesis imperfecta mice. Matrix Biology, 29, 638–644. PMID: 20619344
- Marini, J. (2010). Osteogenesis imperfecta. In F. Singer (Ed.), Diseases of Bone and Calcium Metabolism. Online at http://www.endotext.org/parathyroid/parathyroid17/parathyroidframe17.htm
- Marini, J. C., Letocha, A. D., & Chernoff, E. J. (2005). Osteogenesis imperfecta. In S. B. Cassidy & J.E. Allanson (Eds.), Management of Genetic Syndromes. Hoboken, NJ: Wiley.
- Valli M., Barnes, A., Gallanti, A., Cabral, W., Viglio, S., Weis, M., et al. (2011). Deficiency of CRTAP in nonlethal recessive osteogenesis imperfecta reduces collagen deposition into matrix. Clinical Genetics. PMID: 21955071
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