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Orphanet Journal of Rare Diseases|May 1, 2019
Gynecologic and reproductive outcomes in fibrous dysplasia/McCune-Albright syndromeAlison M Boyce, Rachel K Casey, Diana Ovejero Crespo, et al.The Journal of Clinical Investigation|September 19, 2018
Autoimmune hyperphosphatemic tumoral calcinosis in a patient with FGF23 autoantibodiesMary Scott Roberts, Peter D Burbelo, Daniela Egli-Spichtig, et al.Journal of Surgical Oncology|December 26, 2002
Role of metastasectomy in the management of thyroid carcinoma: the NIH experienceHo Pak, Loukas Gourgiotis, Wen-I Chang, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 19, 2017
Multimodality Image-Guided Cryoablation for Inoperable Tumor-Induced OsteomalaciaSri Harsha Tella, Hayet Amalou, Bradford J Wood, 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.The Journal of Clinical Endocrinology and Metabolism|August 21, 2018
Clinical and Radiographic Gastrointestinal Abnormalities in McCune-Albright SyndromeCemre Robinson, Andrea Estrada, Atif Zaheer, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 8, 2019
Treatment of Autosomal Dominant Hypocalcemia Type 1 With the Calcilytic NPSP795 (SHP635)Mary Scott Roberts, Rachel I Gafni, Beth Brillante, et al.Virology|September 11, 2007
The genome of epsilon15, a serotype-converting, Group E1 Salmonella enterica-specific bacteriophageAndrew M Kropinski, Irina V Kovalyova, Stephen J Billington, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 11, 2016
Phenotypic and Genotypic Characterization and Treatment of a Cohort With Familial Tumoral Calcinosis/Hyperostosis-Hyperphosphatemia SyndromeMary Scott Ramnitz, Pravitt Gourh, Raphaela Goldbach-Mansky, et al.Human Molecular Genetics|September 6, 2013
Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemiaYoung H Lim, Diana Ovejero, Jeffrey S Sugarman, et al.Pageof 19