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Familial Cancer|May 29, 2009
Characterization of the largest kindred with MEN2A due to a Cys609Ser RET mutationCaterina Mian, Susi Barollo, Laura Zambonin, et al.
European Journal of Endocrinology|April 24, 2013
Performance of salivary cortisol in the diagnosis of Cushing's syndrome, adrenal incidentaloma, and adrenal insufficiencyFilippo Ceccato, Mattia Barbot, Marialuisa Zilio, et al.
The Journal of Clinical Endocrinology and Metabolism|June 17, 2008
Case detection, diagnosis, and treatment of patients with primary aldosteronism: an endocrine society clinical practice guidelineJohn W Funder, Robert M Carey, Carlos Fardella, et al.
Journal of Hypertension|April 10, 2008
Liddle's syndrome caused by a novel missense mutation (P617L) of the epithelial sodium channel beta subunitErmanno Rossi, Enrico Farnetti, Anne Debonneville, et al.
The Journal of Clinical Endocrinology and Metabolism|June 30, 2005
Expression profiles for steroidogenic enzymes in adrenocortical diseaseMary H Bassett, Bobbie Mayhew, Khurram Rehman, et al.
Journal of Endocrinological Investigation|November 18, 2025
Postural test to differentiate primary aldosteronism from low-renin hypertension: a retrospective single-center studyIrene Tizianel, Elena Pagin, Eugenio Ragazzi, et al.
Clinical Endocrinology|January 25, 2006
Effect of protracted treatment with rosiglitazone, a PPARgamma agonist, in patients with Cushing's diseaseFrancesca Pecori Giraldi, Carla Scaroni, Emanuela Arvat, et al.
American Journal of Hypertension|August 20, 2005
Analysis of the 11beta-hydroxysteroid dehydrogenase type 2 gene (HSD11B2) in human essential hypertensionBarbara Mariniello, Vanessa Ronconi, Cipriana Sardu, et al.
Surgery|November 20, 2012
Unilateral adrenal hyperplasia: a novel cause of surgically correctable primary hyperaldosteronismMaurizio Iacobone, Marilisa Citton, Giovanni Viel, et al.
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