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Familial Isolated Hyperparathyroidism

Published:2002-01 Issue:1 Volume:81 Page:1-26
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:Medicine

Author:

SIMONDS WILLIAM F.,JAMES-NEWTON LAURA A.,AGARWAL SUNITA K.,YANG BING,SKARULIS MONICA C.,HENDY GEOFFREY N.,MARX STEPHEN J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference109 articles.

1. Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states

2. Markedly reduced activity of mutant calcium-sensing receptor with an inserted Alu element from a kindred with familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

3. Benign schwannoma and parathyroid adenoma occurring in the nonradiated neck: Report of two cases

4. Identification of MEN1 gene mutations in families with MEN 1 and related disorders

Cited by 232 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Familial states of primary hyperparathyroidism: an update;Journal of Endocrinological Investigation;2024-04-18

2. Insights into Hyperparathyroidism–Jaw Tumour Syndrome: From Endocrine Acumen to the Spectrum of CDC73 Gene and Parafibromin-Deficient Tumours;International Journal of Molecular Sciences;2024-02-15

3. Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort;Frontiers in Endocrinology;2023-09-21

4. Draft of clinical guidelines for the diagnosis and treatment of primary hyperparathyroidism in adult patients;Endocrine Surgery;2023-04-07

5. Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome;Case Reports in Dentistry;2023-03-08

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