Multiple brown tumors: a bone complication due to long-term untreated pseudohypoparathyroidism
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s00198-023-06878-5.pdf
Reference15 articles.
1. Mantovani G (2011) Clinical review: pseudohypoparathyroidism: diagnosis and treatment. J Clin Endocrinol Metab 96:3020–3030. https://doi.org/10.1210/jc.2011-1048
2. Eubanks PJ, Stabile BE (1998) Osteitis fibrosa cystica with renal parathyroid hormone resistance: a review of pseudohypoparathyroidism with insight into calcium homeostasis. Arch Surg 133:673–676. https://doi.org/10.1001/archsurg.133.6.673
3. Albright F, Burnett CH, Smith PH, Parson W (1942) Pseudo-hypoparathyroidism-example of “Seabright-Bantam syndrome”; report of three cases. Endocrinology 30:922–932
4. Tashjian AH Jr, Frantz AG, Lee JB (1966) Pseudohypoparathyroidism: assays of parathyroid hormone and thyrocalcitonin. Proc Natl Acad Sci U S A56:1138–1142. https://doi.org/10.1073/pnas.56.4.1138
5. Mann JB, Alterman S, Hills AG (1962) Albright’s hereditary osteodystrophy comprising pseudohypoparathyroidism and pseudo-pseudohypoparathyroidism. With a report of two cases representing the complete syndrome occurring in successive generations. Ann Intern Med 56:315–342. https://doi.org/10.7326/0003-4819-56-2-315
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