Molecular insights into inherited ACTH resistance syndromes
- 31 July 1994
- journal article
- review article
- Published by Elsevier in Trends in Endocrinology & Metabolism
- Vol. 5 (5) , 209-214
- https://doi.org/10.1016/1043-2760(94)90079-5
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Functional Characterization of the Cloned Human ACTH Receptor: Impaired Responsiveness of a Mutant Receptor in Familial Glucocorticoid DeficiencyBiochemical and Biophysical Research Communications, 1993
- Three sibs with achalasia and alacrimia: A separate entity different from triple-A syndromeAmerican Journal of Medical Genetics, 1989
- Autonomic Dysfunction and Adrenocortical Unresponsiveness to ACTHJournal of Child Neurology, 1988
- An ACTH Receptor on Human Mononuclear LeukocytesNew England Journal of Medicine, 1987
- GLOMERULOSA FAILURE IN CONGENITAL ADRENOCORTICAL UNRESPONSIVENESS TO ACTHClinical Endocrinology, 1984
- Absent Aldosterone Response to ACTH in Familial Glucocorticoid DeficiencyNew England Journal of Medicine, 1977
- Familial glucocorticoid insufficiencyThe Journal of Pediatrics, 1973
- Hereditary adrenocortical unresponsiveness to adrenocorticotropic hormoneThe Journal of Pediatrics, 1972
- Adrenocorticotropic hormone unresponsiveness: Report of a girl with excessive growth and review of 16 reported casesThe Journal of Pediatrics, 1972
- A congenital, familial syndrome of adrenocortical insufficiency without hypoaldosteronismThe Journal of Pediatrics, 1960