Familial Benign Hypocalciuric Hypercalcemia and Neonatal Primary Hyperparathyroidism-Reference-Cited by-同舟云学术

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Familial Benign Hypocalciuric Hypercalcemia and Neonatal Primary Hyperparathyroidism

Published:2008 Issue: Volume: Page:1327-1344
ISSN:
Container-title:Principles of Bone Biology
language:
Short-container-title:

Author:

El-Hajj Fuleihan Ghada,Brown Edward M.,Heath Hunter

Publisher

Elsevier

Reference144 articles.

1. Bone mineral density in patients with familial hypocalciuric hypercalcemia (FHH);Abugassa;Eur. J. Surg.,1992

2. Familial hypocalciuric associated with mutation in the human Ca2+-sensing receptor gene;Aida;J. Clin. Endocrinol. Metab,1995

3. Clinical hyperparathyroidism;Albright,1948

4. Une cause rare d'hypercalcemie: L'hypercalcemie hypocalciuriqure familiale;Alexandre;Nouv. Presse Med.,1982

5. Biologically active parathyroid hormone in familial hypocalciuric hypercalcemia;Allgrove;Clin. Endocrinol.,1984

Cited by 4 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 isolated primary hyperparathyroidism due to HRPT2 mutation;Hormones;2013-07

2. Primary Hyperparathyroidism;Endocrine Practice;2012-09

3. Calcium-Sensing Receptor (CASR) Mutations in Hypercalcemic States: Studies from a Single Endocrine Clinic Over Three Years;The Journal of Clinical Endocrinology & Metabolism;2010-04-01

4. Parathyroid Carcinoma, a Rare Entity with Varying Presentation and Treatment;World Journal of Endocrine Surgery;2010

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