ライフサイエンスコーパス: parathyroid carcinoma

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1 rrent hyperparathyroidism after resection of parathyroid carcinoma.

2 on the etiology, diagnosis and treatment of parathyroid carcinoma.

3 parathyroid adenomas but was absent from two parathyroid carcinomas.

4 For the rare patients with parathyroid carcinoma, aggressive surgical resection wit

5 otein, and E-cadherin are useful markers for parathyroid carcinoma and suggest that the presence of a

6 development of non-hereditary and hereditary parathyroid carcinomas, and the hyperparathyroidism-jaw

7 ial pHPT, reoperative parathyroidectomy, and parathyroid carcinoma are challenging entities that requ

8 ll parathyroid neoplasms, including the rare parathyroid carcinoma, are functional and discussion of

9 ncodes the parafibromin protein, in sporadic parathyroid carcinoma because germ-line inactivating HRP

10 Certain patients with apparently sporadic parathyroid carcinoma carry germ-line mutations in HRPT2

11 always benign with an estimated incidence of parathyroid carcinoma causing hyperparathyroidism in onl

12 Sporadic parathyroid carcinomas frequently have HRPT2 mutations t

13 Parathyroid carcinomas from 10 of the 15 patients had HR

14 e-junctional regions of the HRPT2 gene in 21 parathyroid carcinomas from 15 patients who had no known

15 h on the molecular etiology and treatment of parathyroid carcinoma has been slow.

16 A patient with metastatic parathyroid carcinoma in the lungs and pleura developed

17 Parathyroid carcinoma is a rare cause for primary hyperp

18 Parathyroid carcinoma is an extremely rare cause of prim

19 Unexpectedly, HRPT2 mutations in the parathyroid carcinomas of three patients were identified

20 rate loss of heterozygosity more commonly in parathyroid carcinoma than in benign parathyroid lesions

21 The location and extent of the parathyroid carcinoma were correctly detected by PET usi

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