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Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect.
Webb EA, Balasubramanian M, Fratzl-Zelman N, Cabral WA, Titheradge H, Alsaedi A, Saraff V, Vogt J, Cole T, Stewart S, Crabtree NJ, Sargent BM, Gamsjaeger S, Paschalis EP, Roschger P, Klaushofer K, Shaw NJ, Marini JC, Högler W. Webb EA, et al. Among authors: klaushofer k. J Clin Endocrinol Metab. 2017 Jun 1;102(6):2019-2028. doi: 10.1210/jc.2016-3766. J Clin Endocrinol Metab. 2017. PMID: 28323974 Free PMC article.
Bone mass and mineralization in osteogenesis imperfecta.
Fratzl-Zelman N, Misof BM, Klaushofer K, Roschger P. Fratzl-Zelman N, et al. Among authors: klaushofer k. Wien Med Wochenschr. 2015 Jul;165(13-14):271-7. doi: 10.1007/s10354-015-0369-2. Epub 2015 Jul 25. Wien Med Wochenschr. 2015. PMID: 26208477 Review.
Non-Lethal Type VIII Osteogenesis Imperfecta Has Elevated Bone Matrix Mineralization.
Fratzl-Zelman N, Barnes AM, Weis M, Carter E, Hefferan TE, Perino G, Chang W, Smith PA, Roschger P, Klaushofer K, Glorieux FH, Eyre DR, Raggio C, Rauch F, Marini JC. Fratzl-Zelman N, et al. Among authors: klaushofer k. J Clin Endocrinol Metab. 2016 Sep;101(9):3516-25. doi: 10.1210/jc.2016-1334. Epub 2016 Jul 6. J Clin Endocrinol Metab. 2016. PMID: 27383115 Free PMC article.
361 results