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Large Genomic Aberrations in Corticotropinomas Are Associated With Greater Aggressiveness.
Pheochromocytoma in Children and Adolescents With Multiple Endocrine Neoplasia Type 2B.
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline.
Pramlintide but Not Liraglutide Suppresses Meal-Stimulated Glucagon Responses in Type 1 Diabetes.
The Role of Age and Excess Body Mass Index in Progression to Type 1 Diabetes in At-Risk Adults.
Endocrine Treatment of Gender-Dysphoric/Gender-Incongruent Persons: An Endocrine Society Clinical Practice Guideline.
Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease.
Normalized Early Postoperative Cortisol and ACTH Values Predict Nonremission After Surgery for Cushing Disease.
Quantification of Thyroid Cancer and Multinodular Goiter Risk in the DICER1 Syndrome: A Family-Based Cohort Study.
Exome Sequencing Reveals Mutations in AIRE as a Cause of Isolated Hypoparathyroidism.