Primary pigmented nodular adrenocortical disease: the original 4 cases revisited after 30 years for follow-up, new investigations, and molecular genetic findings. [electronic resource]
Producer: 20141009Description: 1266-73 p. digitalISSN:- 1532-0979
- Adolescent
- Adrenal Cortex Diseases -- genetics
- Adrenalectomy
- Biomarkers -- analysis
- Carney Complex -- genetics
- Child
- Cushing Syndrome -- genetics
- Cyclic AMP-Dependent Protein Kinase RIalpha Subunit -- genetics
- Dexamethasone -- administration & dosage
- Female
- Follow-Up Studies
- Gene Deletion
- Genetic Predisposition to Disease
- Humans
- Hydrocortisone -- urine
- Immunohistochemistry
- Male
- Phenotype
- Polymerase Chain Reaction
- Predictive Value of Tests
- Time Factors
- Treatment Outcome
- Young Adult
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Publication Type: Journal Article
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