The Role of Type 1 and Type 2 5′-Deiodinase in the Pathophysiology of the 3,5,3′-Triiodothyronine Toxicosis of McCune-Albright Syndrome-Reference-Cited by-同舟云学术

The Role of Type 1 and Type 2 5′-Deiodinase in the Pathophysiology of the 3,5,3′-Triiodothyronine Toxicosis of McCune-Albright Syndrome

Published:2008-06-01 Issue:6 Volume:93 Page:2383-2389
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Celi Francesco S.¹,Coppotelli Giuseppe¹,Chidakel Aaron¹,Kelly Marilyn²,Brillante Beth A.²,Shawker Thomas³,Cherman Natasha²,Feuillan Penelope P.⁴,Collins Michael T.²

Affiliation:

1. Clinical Endocrinology Branch (F.S.C., G.C., A.C.), National Institutes of Health, Bethesda, Maryland 20892

2. National Institute of Diabetes and Digestive and Kidney Diseases, and Skeletal Clinical Studies Unit (M.K., B.A.B., N.C., M.T.C.), National Institutes of Health, Bethesda, Maryland 20892

3. Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research, Radiology Department (T.S.), National Institutes of Health, Bethesda, Maryland 20892

4. Mark O. Hatfield Clinical Center, National Human Genome Research Institute (P.P.F.), National Institutes of Health, Bethesda, Maryland 20892

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/93/6/2383/9058441/jcem2383.pdf

Reference37 articles.

1. Osteitis fibrosa cystica: the case of a nine-year-old girl who also exhibits precocious puberty, multiple pigmentation of the skin and hyperthyroidism.;McCune;Am J Dis Child,1936

2. Syndrome characterized by osteitis fibrosa disseminata, areas of pigmentation, and endocrine dysfunction, with precocious puberty in females: report of 5 cases.;Albright;N Engl J Med,1937

3. McCune-Albright syndrome;Collins;In: Filetti S, ed.,2004

4. McCune-Albright syndrome.;Feuillan;Curr Ther Endocrinol Metab,1997

5. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome.;Weinstein;N Engl J Med,1991

Cited by 53 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. The first case report of McCune-Albright syndrome in Syria with late diagnosis;Journal of Clinical and Translational Endocrinology: Case Reports;2024-03

2. Thyroid hormone action and liver disease, a complex interplay;Hepatology;2023-08-02

3. Case report: Surgical treatment of McCune-Albright syndrome with hyperthyroidism and retrosternal goiter: A case report and literature review;Frontiers in Surgery;2023-01-06

4. Interpretation, differential diagnosis, and clinical implications of abnormal thyroid function tests in children;Trends in Pediatrics;2023

5. Mccune-Albright Syndrome;Asian Journal of Nursing Education and Research;2022-08-01