Zobrazeno 1 - 10
of 128
pro vyhledávání: '"Edward G. Biglieri"'
Autor:
Edward G. Biglieri
Publikováno v:
Steroids. 60:52-58
In the course of my studies of patients with mineralocorticoid hypertensive disorders, unusual presentations led to unexpected findings, both clinically and in steroid etiologies and regulation. Unique circumstances permitted early studies in definin
Autor:
Claudio E. Kater, Edward G. Biglieri
Publikováno v:
Endocrinology and Metabolism Clinics of North America. 23:341-357
This article reviews some clinical and biochemical aspects of the 17a-hydroxylase/17,20-lase deficiency. The authors data, obtained from 20 patients that are virtually all hypogonadic females or male pseudohermaphrodites with hypertension and hypokal
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 42:617-623
Continued administration of ACTH to patients with hypopituitarism produced normal increases in steroids dependent on microsomal cytochrome P 450 21 and P 450 17 α but reduced responses of steroids dependent on mitochondrial cytochrome P 450 11 β
Autor:
Ilan Irony, Rosita Gomez-Fontes, Robert V. Farese, Cedric H. L. Shackleton, Edward G. Biglieri
Publikováno v:
New England Journal of Medicine. 325:1223-1227
EXCESSIVE ingestion of licorice may result in sodium and water retention, hypertension, hypokalemia, and suppression of the renin-aldosterone system.1 , 2 It was thought for years that licorice produced these effects through the binding of its active
Autor:
Claudio E. Kater, Edward G. Biglieri
Publikováno v:
Endocrinology and Metabolism Clinics of North America. 20:257-268
Cases of sexual immaturity and male pseudohermaphroditism due to disorders such as androgen resistance, 5 alpha-reductase deficiency, cholesterol desmolase deficiency, 3 beta-hydroxysteroid dehydrogenase deficiency, and testicular and ovary dysgenesi
Publikováno v:
American Journal of Hypertension. 3:576-582
Among 154 cases of primary aldosteronism seen in the General Clinical Research Center at San Francisco General Hospital, twelve patients did not fulfill established characteristics of an aldosterone producing adenoma (APA) or idiopathic hyperaldoster
Autor:
Edward G. Biglieri
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:48-50
Autor:
Claudio E. Kater, Edward G. Biglieri
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia v.48 n.5 2004
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 48, Issue: 5, Pages: 674-681, Published: OCT 2004
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 48, Issue: 5, Pages: 674-681, Published: OCT 2004
Primary aldosteronism (PA) is characterized by hypertension and suppressed renin activity with or without hypokalemia and comprises the aldosterone-producing adenoma (APA) and bilateral adrenal hyperplasia or idiopatic hyperaldosteronism (IHA). In re
Publikováno v:
The Journal of clinical endocrinology and metabolism. 71(2)
Short term suppression of ACTH by dexamethasone effects limited reduction in plasma deoxycorticosterone (DOC) while cortisol levels are almost completely suppressed in normal control subjects. The zona fasciculata (ZF) microsomal cytochrome P-450(21)
Publikováno v:
Journal of Steroid Biochemistry. 9:495-505
Urinary steroids from a patient with 17α-hydroxylase deficiency syndrome have been identified. The steroids were obtained by enzymatic hydrolysis of urine, Amberlite XAD-2 extraction and Sephadex LH-20 column chromatography. Following preparation of