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Parathyroid Carcinoma and Persistent Hypercalcemia: A Case Report and Review of Therapeutic Options
Parathyroid carcinomas are very uncommon, accounting for 0.1% to 5% of all causes of primary hyperparathyroidism. Parathyroid–jaw tumor syndrome, with a mutation in HRPT2 that encodes parafibromin, is the most common genetic association. Unique features include aggressive clinical course and a lack...
Gorde:
| Argitaratua izan da: | Saudi J Med Med Sci |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Medknow Publications & Media Pvt Ltd
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6196698/ https://ncbi.nlm.nih.gov/pubmed/30787833 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/sjmms.sjmms_104_16 |
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