Journal of Endocrinological Investigation
3 Articles
- A Novel Deletion Mutation in the Arginine Vasopressin Receptor 2 Gene and Skewed X Chromosome Inactivation in a Female Patient with Congenital Nephrogenic Diabetes Insipidus
- Acquired Nephrogenic Diabetes Insipidus Secondary to Distal Renal Tubular Acidosis and Nephrocalcinosis Associated with Sjogren's Syndrome
- Impairment of AVP Regulation in 17alpha-Hydroxylase Deficiency, a Unique Form of Adrenal Insufficiency