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Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 5, 2021
Clinical and molecular characterization of Chilean patients with X-linked hypophosphatemiaM Jiménez, D Ivanovic-Zuvic, C Loureiro, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 31, 2018
Tumor-induced osteomalacia in association with PTEN-negative Cowden syndromeJ A Berglund, R I Gafni, F Wodajo, et al.JAMA|March 22, 1995
Apolipoprotein E type 4 allele and cerebral glucose metabolism in relatives at risk for familial Alzheimer diseaseG W Small, J C Mazziotta, M T Collins, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 5, 2008
A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic featuresC E Dumitrescu, M H Kelly, A Khosravi, et al.Journal of Dental Research|April 5, 2014
Rare bone diseases and their dental, oral, and craniofacial manifestationsB L Foster, M S Ramnitz, R I Gafni, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 26, 2000
Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of boneP Bianco, M Riminucci, A Majolagbe, et al.Archives of Osteoporosis|March 1, 2017
Improving patient outcomes in fibrous dysplasia/McCune-Albright syndrome: an international multidisciplinary workshop to inform an international partnershipA M Boyce, A Turner, L Watts, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 8, 2016
Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatmentD Ovejero, Y H Lim, A M Boyce, et al.Journal of Dental Research|December 16, 2017
Hypercementosis Associated with ENPP1 Mutations and GACIV Thumbigere-Math, A Alqadi, N I Chalmers, et al.Physical Review Letters|March 22, 2021
Constraints on Dark Matter Properties from Observations of Milky Way Satellite GalaxiesE O Nadler, A Drlica-Wagner, K Bechtol, et al.Pageof 15