|
Adrenal and Hypertension
Contributing journals to this collection:
Journal of Clinical Endocrinology & Metabolism,
Molecular Endocrinology,
Endocrinology,
Endocrine Reviews,
and Endocrine Society Journals
Citations 461-470 of 496 total displayed.
- Endocrine Care
Urinary Markers of Adrenarche: Reference Values in Healthy Subjects, Aged 3–18 Years
- Thomas Remer, Kai R. Boye, Michaela F. Hartmann, and Stefan A. Wudy
J. Clin. Endocrinol. Metab. 90: 2015 -2021; published online before print as doi:10.1210/jc.2004-1571
[Abstract]
[Full text]
- Endocrine Care
Biochemical and Clinical Manifestations of Dopamine-Producing Paragangliomas: Utility of Plasma Methoxytyramine
- Graeme Eisenhofer, David S. Goldstein, Patricia Sullivan, Gyorgy Csako, Frederieke M. Brouwers, Edwin W. Lai, Karen T. Adams, and Karel Pacak
J. Clin. Endocrinol. Metab. 90: 2068 -2075; published online before print as doi:10.1210/jc.2004-2025
[Abstract]
[Full text]
- Endocrine Care
Delayed Diagnosis of Congenital Adrenal Hyperplasia with Salt Wasting Due to Type II 3ß-Hydroxysteroid Dehydrogenase Deficiency
- Trine H. Johannsen, Delphine Mallet, Harriet Dige-Petersen, Jørn Müller, Katharina M. Main, Yves Morel, and Maguelone G. Forest
J. Clin. Endocrinol. Metab. 90: 2076 -2080; published online before print as doi:10.1210/jc.2004-1374
[Abstract]
[Full text]
- Endocrine Care
Year of Diagnosis, Features at Presentation, and Risk of Recurrence in Patients with Pheochromocytoma or Secreting Paraganglioma
- Laurence Amar, Aude Servais, Anne-Paule Gimenez-Roqueplo, Franck Zinzindohoue, Gilles Chatellier, and Pierre-François Plouin
J. Clin. Endocrinol. Metab. 90: 2110 -2116; published online before print as doi:10.1210/jc.2004-1398
[Abstract]
[Full text]
- Other Original Articles
Not All Amino Acid Substitutions of the Common Cluster E6 Mutation in CYP21 Cause Congenital Adrenal Hyperplasia
- Tiina Robins, Michela Barbaro, Svetlana Lajic, and Anna Wedell
J. Clin. Endocrinol. Metab. 90: 2148 -2153; published online before print as doi:10.1210/jc.2004-1937
[Abstract]
[Full text]
- Other Original Articles
ß2-Adrenergic Receptor Polymorphisms and Salbutamol-Stimulated Energy Expenditure
- J. M. Oomen, C. T. M. van Rossum, B. Hoebee, W. H. M. Saris, and M. A. van Baak
J. Clin. Endocrinol. Metab. 90: 2301 -2307; published online before print as doi:10.1210/jc.2004-1356
[Abstract]
[Full text]
- Other Original Articles
Elevated Serum Interferon- -Inducible Chemokine-10/CXC Chemokine Ligand-10 in Autoimmune Primary Adrenal Insufficiency and in Vitro Expression in Human Adrenal Cells Primary Cultures after Stimulation with Proinflammatory Cytokines
- Mario Rotondi, Alberto Falorni, Annamaria De Bellis, Stefano Laureti, Pietro Ferruzzi, Paola Romagnani, Andrea Buonamano, Elena Lazzeri, Clara Crescioli, Massimo Mannelli, Fausto Santeusanio, Antonio Bellastella, and Mario Serio
J. Clin. Endocrinol. Metab. 90: 2357 -2363; published online before print as doi:10.1210/jc.2004-1062
[Abstract]
[Full text]
- Endocrine Care
Refining Hormonal Diagnosis of Type II 3ß-Hydroxysteroid Dehydrogenase Deficiency in Patients with Premature Pubarche and Hirsutism Based on HSD3B2 Genotyping
- Livia M. Mermejo, Lucila L. K. Elias, S. Marui, Ayrton C. Moreira, Berenice B. Mendonca, and Margaret de Castro
J. Clin. Endocrinol. Metab. 90: 1287 -1293; published online before print as doi:10.1210/jc.2004-1552
[Abstract]
[Full text]
- Endocrine Care
In Vivo and in Vitro Screening for Illegitimate Receptors in Adrenocorticotropin-Independent Macronodular Adrenal Hyperplasia Causing Cushing’s Syndrome: Identification of Two Cases of Gonadotropin/Gastric Inhibitory Polypeptide-Dependent Hypercortisolism
- Jérôme Bertherat, Vincent Contesse, Estelle Louiset, Gaëlle Barrande, Céline Duparc, Lionel Groussin, Philippe Émy, Xavier Bertagna, Jean-Marc Kuhn, Hubert Vaudry, and Hervé Lefebvre
J. Clin. Endocrinol. Metab. 90: 1302 -1310; published online before print as doi:10.1210/jc.2004-1256
[Abstract]
[Full text]
- Endocrine Care
Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by TPIT Gene Mutations
- Sophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino, Magali Gueydan, Anne Barlier, Michel David, Marc Nicolino, Georges Malpuech, Pierre Déchelotte, Cheri Deal, Guy Van Vliet, Monique De Vroede, Felix G. Riepe, Carl-Joachim Partsch, Wolfgang G. Sippell, Merih Berberoglu, Begüm Atasay, Francis de Zegher, Dominique Beckers, Jennifer Kyllo, Patricia Donohoue, Martin Fassnacht, Stefanie Hahner, Bruno Allolio, C. Noordam, Leo Dunkel, Matti Hero, B. Pigeon, Jacques Weill, Sevket Yigit, Raja Brauner, Juan Jorge Heinrich, Elizabeth Cummings, Christie Riddell, Alain Enjalbert, and Jacques Drouin
J. Clin. Endocrinol. Metab. 90: 1323 -1331; published online before print as doi:10.1210/jc.2004-1300
[Abstract]
[Full text]
|
|
