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2004 2
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ACTH-independent macronodular adrenal hyperplasia.
Lacroix A. Lacroix A. Best Pract Res Clin Endocrinol Metab. 2009 Apr;23(2):245-59. doi: 10.1016/j.beem.2008.10.011. Best Pract Res Clin Endocrinol Metab. 2009. PMID: 19500767 Review.
Adrenocorticotropic hormone- (ACTH-)independent macronodular adrenal hyperplasia (AIMAH) is an infrequent cause of Cushing's syndrome (CS). ...
Adrenocorticotropic hormone- (ACTH-)independent macronodular adrenal hyperplasia (AIMAH) is an infrequent …
Genetics of primary macronodular adrenal hyperplasia.
Fragoso MC, Alencar GA, Lerario AM, Bourdeau I, Almeida MQ, Mendonca BB, Lacroix A. Fragoso MC, et al. J Endocrinol. 2015 Jan;224(1):R31-43. doi: 10.1530/JOE-14-0568. J Endocrinol. 2015. PMID: 25472909 Review.
ACTH-independent macronodular adrenal hyperplasia is a rare cause of Cushing's syndrome (CS), accounting for <2% of all endogenous CS cases; however it is more frequently identified incidentally with sub-clinical cortisol secretion. ..
ACTH-independent macronodular adrenal hyperplasia is a rare cause of Cushing's syndrome (CS), accounting
Primary bilateral macronodular adrenal hyperplasia.
De Venanzi A, Alencar GA, Bourdeau I, Fragoso MC, Lacroix A. De Venanzi A, et al. Curr Opin Endocrinol Diabetes Obes. 2014 Jun;21(3):177-84. doi: 10.1097/MED.0000000000000061. Curr Opin Endocrinol Diabetes Obes. 2014. PMID: 24739311 Review.
The recent finding of ectopic adrenocortical production of adrenocorticotropic hormone in clusters of bilateral macronodular adrenal hyperplasia tissues and its regulation by aberrant hormone receptors opens new horizons for eventual medical therapy using melanocortin-2 re …
The recent finding of ectopic adrenocortical production of adrenocorticotropic hormone in clusters of bilateral macronodular adrenal hyperpl …
Clinical and molecular genetic studies of bilateral adrenal hyperplasias.
Bourdeau I. Bourdeau I. Endocr Res. 2004 Nov;30(4):575-83. doi: 10.1081/erc-200043735. Endocr Res. 2004. PMID: 15666794 Review.
ACTH-independent, cortisol-producing hyperplasia is caused by 2 distinct disorders, primary pigmented nodular adrenocortical disease (PPNAD) and ACTH-independent macronodular adrenal hyperplasia (AIMAH). ...
ACTH-independent, cortisol-producing hyperplasia is caused by 2 distinct disorders, primary pigmented nodular adrenocortical disease …
CT and MR imaging of the adrenal glands in ACTH-independent cushing syndrome.
Rockall AG, Babar SA, Sohaib SA, Isidori AM, Diaz-Cano S, Monson JP, Grossman AB, Reznek RH. Rockall AG, et al. Radiographics. 2004 Mar-Apr;24(2):435-52. doi: 10.1148/rg.242035092. Radiographics. 2004. PMID: 15026592 Review.
Bilateral disease--primary pigmented nodular adrenal dysplasia (PPNAD) (n = 2) and ACTH-independent macronodular adrenal hyperplasia (AIMAH) (n = 1)--had characteristic imaging features. In PPNAD, multiple tiny (2-5-mm) nodules wer …
Bilateral disease--primary pigmented nodular adrenal dysplasia (PPNAD) (n = 2) and ACTH-independent macronodular
Molecular genetics of adrenocortical tumor formation and potential pharmacologic targets.
Rauschecker M, Stratakis CA. Rauschecker M, et al. Minerva Endocrinol. 2012 Jun;37(2):133-9. Minerva Endocrinol. 2012. PMID: 22691887 Free PMC article. Review.
Mutations in the G-protein coupled receptor are associated with McCune-Albright syndrome and ACTH-independent macronodular adrenal hyperplasia, while defects in cAMP-dependent protein kinase A can lead to the development of Carney's complex, as …
Mutations in the G-protein coupled receptor are associated with McCune-Albright syndrome and ACTH-independent macronodular
Pharmacologic management of Cushing syndrome : new targets for therapy.
Sonino N, Boscaro M, Fallo F. Sonino N, et al. Treat Endocrinol. 2005;4(2):87-94. doi: 10.2165/00024677-200504020-00003. Treat Endocrinol. 2005. PMID: 15783246 Review.
In GIP-dependent Cushing syndrome, the most frequent subtype of ACTH-independent macronodular adrenal hyperplasia associated with the presence of aberrant adrenocortical hormone receptors described so far, octreotide administration before each m …
In GIP-dependent Cushing syndrome, the most frequent subtype of ACTH-independent macronodular adrenal hyperpl
Challenges in the diagnostic work-up and management of patients with subclinical Cushing's syndrome and bilateral adrenal masses.
Maghrabi A, Yaqub A, Denning KL, Benhamed N, Faiz S, Saleem T. Maghrabi A, et al. Endocr Pract. 2013 May-Jun;19(3):515-21. doi: 10.4158/EP12277.RA. Endocr Pract. 2013. PMID: 23425643 Review.
OBJECTIVE: To review the challenges encountered in the diagnostic work-up and management of patients with subclinical Cushing's syndrome (SCS) and bilateral adrenal masses to aid in the case description of a patient with SCS and adrenocorticotropic hormone (ACTH)-indepe
OBJECTIVE: To review the challenges encountered in the diagnostic work-up and management of patients with subclinical Cushing's syndrome (SC …
Long delay in diagnosis of a case with MEN1 due to concomitant presence of AIMAH with insulinoma: a case report and literature review.
Chavoshi V, Tamehri Zadeh SS, Khalili S, Rabbani A, Matini SAH, Mohsenifar Z, Hadaegh F. Chavoshi V, et al. BMC Endocr Disord. 2022 Apr 21;22(1):108. doi: 10.1186/s12902-022-01022-6. BMC Endocr Disord. 2022. PMID: 35448982 Free PMC article. Review.
Genetic abnormalities in the MEN1, heterozygote for pathogenic variant chr11; 645,773,330-64577333AGAC, c.249-252delGTCT, p. (11e85Serfs Ter33) in exon 2 were found. It was recommended the patient undergoes parathyroidectomy as soon as possible. ...
Genetic abnormalities in the MEN1, heterozygote for pathogenic variant chr11; 645,773,330-64577333AGAC, c.249-252delGTCT, p. (11e85Serfs Ter …
11 results