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See Latest ArticlesCongenital adrenal hyperplasia in adults
Expert Review of Endocrinology & Metabolism, 01/21/09
Lin-Su K et al. - Hyperandrogenism in congenital adrenal hyperplasia (CAH) results from overstimulation of adrenocorticotropic-driven androgen production in the adrenal cortex due to lack of cortisol feedback. The goal of therapy in CAH is to both correct the deficiency in cortisol secretion and suppress androgen overproduction. Glucocorticoid replacement has been the mainstay of treatment for CAH but new treatment strategies continue to be developed and studied.
Today in Adrenal Glands...keeping you current
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Adrenocorticotrophic hormone secreting pheochromocytoma
Indian Journal of Urology, 03/19/10
Growth Impairment in a Boy with Late-Onset Congenital Adrenal Hyperplasia and Anorexia Nervosa
Experimental and Clinical Endocrinology & Diabetes, 03/19/10
Phaeochromocytoma-associated critical peripheral ischaemia
Internal Medicine Journal, 03/19/10
Today in Neuroendocrinology...keeping you current
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Modulatory Effect of Raloxifene and Estrogen on the Metabolic Action of Growth Hormone in Hypopituitary Women
Journal of Clinical Endocrinology and Metabolism, 03/19/10
A technical note on endonasal combined microscopic endoscopic with free head navigation technique of removal of pituitary adenomas
Neurosurgical Review, 03/19/10
Value of combined 6-[18F]fluorodihydroxyphenylalanine PET/CT for imaging of neuroendocrine tumours
British Journal of Surgery, 03/18/10
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