Mechanisms establishing the mineralocorticoid hormone patterns in the 17 alpha-hydroxylase deficiency syndrome.
作者信息
Biglieri E G
出版信息
J Steroid Biochem. 1979 Jul;11(1B):653-7. doi: 10.1016/0022-4731(79)90095-5.
PMID:226795
Abstract
摘要
相似文献
1
Mechanisms establishing the mineralocorticoid hormone patterns in the 17 alpha-hydroxylase deficiency syndrome.
J Steroid Biochem. 1979 Jul;11(1B):653-7. doi: 10.1016/0022-4731(79)90095-5.
2
The unique patterns of plasma aldosterone and 18-hydroxycorticosterone concentrations in the 17 alpha-hydroxylase deficiency syndrome.
J Clin Endocrinol Metab. 1982 Aug;55(2):295-302. doi: 10.1210/jcem-55-2-295.
3
The zonal origins of the mineralocorticoid hormones in the 21-hydroxylation deficiency of congenital adrenal hyperplasia.
J Clin Endocrinol Metab. 1981 Nov;53(5):964-9. doi: 10.1210/jcem-53-5-964.
4
17 alpha-hydroxylase deficiency: mineralocorticoid hormone profiles in an affected family.
J Clin Endocrinol Metab. 1983 Apr;56(4):697-701. doi: 10.1210/jcem-56-4-697.
5
Impaired mineralocorticoid hormone responses to adrenocorticotropin stimulation: additional characterization of heterozygosity for the 21-hydroxylase deficiency type of congenital adrenal hyperplasia.
J Clin Endocrinol Metab. 1983 Nov;57(5):1061-6. doi: 10.1210/jcem-57-5-1061.
6
Effects of continued adrenocorticotropin stimulation on the mineralocorticoid hormones in classical and nonclassical simple virilizing types of 21-hydroxylase deficiency.
J Clin Endocrinol Metab. 1985 Jun;60(6):1057-62. doi: 10.1210/jcem-60-6-1057.
7
Distinctive plasma aldosterone, 18-hydroxycorticosterone, and 18-hydroxydeoxycorticosterone profile in the 21-, 17 alpha-, and 11 beta-hydroxylase deficiency types of congenital adrenal hyperplasia.
Am J Med. 1983 Jul;75(1):43-8. doi: 10.1016/0002-9343(83)91166-x.
8
Adrenocorticotropin inhibition of mineralocorticoid hormone production.
Clin Sci (Lond). 1979 Dec;57 Suppl 5:307s-311s. doi: 10.1042/cs057307s.
9
[Mineralocorticoid functional exploration in two cases of 11 beta OH corticosteroid deficiency].
Ann Endocrinol (Paris). 1974 May-Jun;35(3):247-54.
10
[A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency with high levels of plasma aldosterone and angiotensin II].
Nihon Sanka Fujinka Gakkai Zasshi. 1986 Jul;38(7):1162-5.
引用本文的文献
1
Functional Identification of Compound Heterozygous Mutations in the Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency.
Endocrinol Metab (Seoul). 2018 Sep;33(3):413-422. doi: 10.3803/EnM.2018.33.3.413.
2
Steroid enzyme defects leading to male pseudohermaphroditism.
Indian J Pediatr. 1992 Jul-Aug;59(4):501-14. doi: 10.1007/BF02751568.
Zotero 插件