ACTH Resistance Syndromes
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1345-2
Reference13 articles.
1. Allgrove J, Clayden GS, Grant DB et al (1978) Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production. Lancet (London, England) 1(8077):1284–1286. https://doi.org/10.1016/s0140-6736(78)91268-0
2. Chan LF, Clark AJL, Metherell LA (2008) Familial glucocorticoid deficiency: advances in the molecular understanding of ACTH action. Horm Res Paediatr 69:75–82. https://doi.org/10.1159/000111810
3. Clark AJ, McLoughlin L, Grossman A (1993) Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor. Lancet (London, England) 341(8843):461–462. https://doi.org/10.1016/0140-6736(93)90208-x
4. Flokas ME, Tomani M, Agdere L, Brown B (2019) Triple a syndrome (Allgrove syndrome): improving outcomes with a multidisciplinary approach. Pediatr Health Med Ther 10:99–106. https://doi.org/10.2147/PHMT.S173081
5. Fujieda K, Tajima T (2005) Molecular basis of adrenal insufficiency. Pediatr Res 57:62R–69R. https://doi.org/10.1203/01.PDR.0000159568.31749.4D
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