DISORDERS OF STEROID 11-BETA-HYDROXYLASE ISOZYMES

被引：239
作者：
WHITE, PC [1 ]
CURNOW, KM [1 ]
PASCOE, L [1 ]
机构：
[1] CORNELL UNIV, COLL MED, DEPT PEDIAT, NEW YORK, NY 10021 USA
来源：
ENDOCRINE REVIEWS | 1994年 / 15卷 / 04期
关键词：
D O I：
10.1210/er.15.4.421
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：421 / 438
页数：18
相关论文
共 210 条
[1]   ADRENOGENITAL SYNDROME DUE TO 11-BETA-HYDROXYLASE DEFICIENCY WITH SKELETAL ABNORMALITIES AND PULMONARY STENOSIS [J].
AJLOUNI, K ;
ELZAHERI, M ;
HABBAB, M ;
QOUSSOUS, Y ;
ELKHATEEB, M .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1984, 7 (02) :129-131
[2]   MUTATION IN THE CYP21B GENE (ILE-172-]ASN) CAUSES STEROID 21-HYDROXYLASE DEFICIENCY [J].
AMOR, M ;
PARKER, KL ;
GLOBERMAN, H ;
NEW, MI ;
WHITE, PC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (05) :1600-1604
[3]  
AZZIZ R, 1991, FERTIL STERIL, V55, P733
[4]   21-HYDROXYLASE DEFICIENCY IN FEMALE HYPERANDROGENISM - SCREENING AND DIAGNOSIS [J].
AZZIZ, R ;
ZACUR, HA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 69 (03) :577-584
[5]  
BAKER SW, 1981, PEDIATR ADOLESC ENDO, V8, P261
[6]   THE CORTICOSTEROID EXCRETION PATTERN IN INFANTS AND CHILDREN WITH THE ADRENOGENITAL SYNDROME [J].
BERGSTRAND, CG ;
BIRKE, G ;
PLANTIN, LO .
ACTA ENDOCRINOLOGICA, 1959, 30 (04) :500-508
[7]   HUMAN NCI-H295 ADRENOCORTICAL CARCINOMA-CELLS - A MODEL FOR ANGIOTENSIN-II-RESPONSIVE ALDOSTERONE SECRETION [J].
BIRD, IM ;
HANLEY, NA ;
WORD, RA ;
MATHIS, JM ;
MCCARTHY, JL ;
MASON, JI ;
RAINEY, WE .
ENDOCRINOLOGY, 1993, 133 (04) :1555-1561
[8]  
BIRNBAUM MD, 1984, OBSTET GYNECOL, V63, P445
[9]  
BISTRITZER T, 1984, ISRAEL J MED SCI, V20, P55
[10]   ADRENOGENITAL SYNDROME (11-BETA-HYDROXYLASE DEFICIENCY) WITH HYPERPROLACTINEMIA - REVERSAL BY GLUCOCORTICOID ADMINISTRATION [J].
BRAUTBAR, NN ;
BENDAVID, MM .
ARCHIVES OF INTERNAL MEDICINE, 1977, 137 (11) :1608-1609
12345678910