Mostrando 10 resultados de: 24
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Journal of Clinical Endocrinology and Metabolism(7)
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Hypertension(2)
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Enfermedades(22)
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scopus(24)
Clinical syndromes of hormone receptor mutations: Hormone resistance and independence
ArticleAbstract: Clinical syndromes of hormone resistance or independence have baffled clinicians for decades. ThesePalabras claves:Glycollate, Hormone receptors, Sodium pentosan polysulphateAutores:Fuqua S.A.W., Richard J. AuchusFuentes:scopusAN INDIVIDUALIZED APPROACH TO THE EVALUATION AND MANAGEMENT OF PRIMARY ALDOSTERONISM
ReviewAbstract: OBJECTIVE: With the increased emphasis on personalized and individualized medicine, the American AssPalabras claves:Autores:Malchoff C.D., Richard J. Auchus, Vaidya A.Fuentes:scopusCongenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
ReviewAbstract: Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders affecting cortisolPalabras claves:21-hydroxylase deficiency, aldosterone, cortisol, CYP21A2, Glucocorticoid, mineralocorticoid, Steroid biosynthesisAutores:Arlt W., Faisal Ahmed S., Falhammar H., Flück C.E., Guasti L., Huebner A., Kortmann B.B.M., Krone N., Merke D.P., Miller W.L., Nordenström A., Reisch N., Richard J. Auchus, Sandberg D.E., Speiser P.W., Stikkelbroeck N.M.M.L., Touraine P., Utari A., van der Grinten H.L.C., White P.C., Wudy S.A.Fuentes:scopusCongenital adrenal hyperplasia in adults
ReviewAbstract: Purpose of Review: Patients born with congenital adrenal hyperplasia (CAH), the majority of which isPalabras claves:21-hydroxylase deficiency, 46XX DSD, Adrenal gland, androgen, Congenital adrenal hyperplasia, steroidogenesis, Testicular adrenal rest tissue, VirilizationAutores:Richard J. AuchusFuentes:scopusConsensus on diagnosis and management of Cushing's disease: a guideline update
ReviewAbstract: Cushing's disease requires accurate diagnosis, careful treatment selection, and long-term managementPalabras claves:Autores:Bancos I., Ben-Shlomo A., Bertherat J., Biermasz N.R., Biller B.M.K., Boguszewski C.L., Bronstein M.D., Buchfelder M., Carmichael J.D., Casanueva F.F., Castinetti F., Chanson P., Findling J.W., Fleseriu M., Gadelha M., Geer E.B., Giustina A., Grossman A., Gurnell M., Ho K., Ioachimescu A.G., Kaiser U.B., Karavitaki N., Katznelson L., Kelly D.F., Lacroix A., McCormack A.I., Melmed S., Molitch M., Mortini P., Newell-Price J., Nieman L.K., Pereira A.M., Petersenn S., Pivonello R., Raff H., Reincke M., Richard J. Auchus, Salvatori R., Scaroni C., Shimon I., Stratakis C.A., Swearingen B., Tabarin A., Takahashi Y., Theodoropoulou M., Tsagarakis S., Valassi E., Varlamov E.V., Vila G., Wass J., Webb S.M., Zatelli M.C.Fuentes:scopusDefects in androgen biosynthesis causing 46,XY disorders of sexual development
ArticleAbstract: At least one genetic defect in each reaction of the classical androgen biosynthesis pathway has beenPalabras claves:46 XY DSD, androgen, Congenital adrenal hyperplasia, Enzyme, Steroid, steroidogenesis, Testis, TestosteroneAutores:Miller W.L., Richard J. AuchusFuentes:scopusApproach to the patient: The adult with congenital adrenal hyperplasia
ReviewAbstract: The most common form of congenital adrenal hyperplasia is steroid 21-hydroxylase deficiency (21OHD).Palabras claves:Autores:Arlt W., Richard J. AuchusFuentes:scopusAn International Consortium Update: Pathophysiology, Diagnosis, and Treatment of Polycystic Ovarian Syndrome in Adolescence
ReviewAbstract: This paper represents an international collaboration of paediatric endocrine and other societies (liPalabras claves:Anti-androgen, Hirsutism, Hyperinsulinism, Insulin sensitizers, Menstrual irregularities, obesity, Polycystic ovarian morphology, Polycystic ovary syndromeAutores:Alkhayyat H., Chang R.J., Codner E., Dabadghao P., Darendeliler F., De Zegher F., Deeb A., Elbarbary N.S., Gambineri A., Garcia Rudaz C., Hoeger K.M., Horikawa R., Ibáñez L., Joel D., Lee P.A., López-Bermejo A., Oberfield S.E., Ong K., Peña A.S., Reinehr T., Richard J. Auchus, Santoro N., Tao R., Tena-Sempere M., Witchel S., Yildiz B.O.Fuentes:scopusGlucocorticoid Withdrawal Syndrome following treatment of endogenous Cushing Syndrome
ReviewAbstract: Purpose:: Literature regarding endogenous Cushing syndrome (CS) largely focuses on the challenges ofPalabras claves:Adrenal insufficiency, Corticosteroid withdrawal syndrome, Cushing disease, Cushing syndrome, Glucocorticoid withdrawal syndrome, Steroid withdrawal syndromeAutores:Findling J.W., He X., Richard J. AuchusFuentes:scopusEpithelial sodium channel allele T594M is not associated with blood pressure or blood pressure response to amiloride
ArticleAbstract: The T594M allele of the epithelial sodium channel β-subunit has been proposed as a gain-of-functionPalabras claves:Hypertension, genetic, ion channels, SodiumAutores:Bell D.M., Chirachanchai M.G., Cooper R.S., Hollier J.M., Leonard D., Li J.L., Martin D.F., McKenzie C., Menon D.V., Richard J. Auchus, Victor R.G., Wu X.Fuentes:scopus