Pituitary corticotroph adenoma in a woman with long-standing addison’s disease: A histologic, immunocytochemical, electron microscopic, andIn Situ hybridization study-Reference-Cited by-同舟云学术

Pituitary corticotroph adenoma in a woman with long-standing addison’s disease: A histologic, immunocytochemical, electron microscopic, andIn Situ hybridization study

Published:1996-02 Issue:1 Volume:7 Page:91-97
ISSN:1046-3976
Container-title:Endocrine Pathology
language:en
Short-container-title:Endocr Pathol

Author:

Kovacs Kalman,Stefaneanu Lucia,Horvath Eva,Buchfelder Michael,Fahlbusch Rudolph,Althoff Peter H.,Moore Christine

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF02739919.pdf

Reference24 articles.

1. Krieger DT, Gewirtz GD. The nature of the circadian periodicity and suppressibility of immunoreactive ACTH levels in Addison’s disease. J Clin Endocrinol Metab 39:46–52, 1974.

2. Scott RS, Donald RA, Espiner EA. Plasma ACTH and cortisol profiles in Addisonian patients receiving conventional substitution therapy. Clin Endocrinol 9:571–576, 1978.

3. Feek CM, Ratcliffe JG, Seth J, Gray CE, Toft AD, Irvine WJ. Patterns of plasma cortisol and ACTH concentrations in patients with Addison’s disease treated with conventional corticosteroid replacement. Clin Endocrinol 14:451–458, 1981.

4. Dluhy RG, Moore TJ, Williams GH. Sella turcica enlargement and primary adrenal insufficiency. Ann Intern Med 89:513,514, 1978.

5. Carr DB, Fisher JE, Rosenblatt M. Response to low-dose pulsatile cortisol in Addison’s disease with suspected corticotropinoma. Horm Metabol Res 18:569–573, 1986.

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