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74 in total

1. [Congenital adrenal hyperplasia due to blockade of 3-beta-hydroxysteroid dehydrogenase].

Authors: D Gendrel; J L Chaussain; M Roger; J C Job
Journal: Arch Fr Pediatr Date: 1979 Jul-Aug

2. Persistent testicular delta5-isomerase-3beta-hydroxysteroid dehydrogenase (delta5-3beta-HSD) deficiency in the delta5-3beta-HSD form of congenital adrenal hyperplasia.

Authors: G Schneider; M Genel; A M Bongiovanni; A S Goldman; R L Rosenfield
Journal: J Clin Invest Date: 1975-04 Impact factor: 14.808

3. Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a stop codon in the N-terminal region of 17 alpha-hydroxylase cytochrome P-450.

Authors: T Yanase; M Kagimoto; N Matsui; E R Simpson; M R Waterman
Journal: Mol Cell Endocrinol Date: 1988-10 Impact factor: 4.102

4. [Congenital adrenal hyperplasia; 21-hydroxylase-deficiency combined with 17-desmolase-deficiency (author's transl)].

Authors: H Gleispach; H Berger; J Glatzl; H Rössler
Journal: Padiatr Padol Date: 1974

5. Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: molecular basis of one example of combined 17 alpha-hydroxylase/17,20 lyase deficiency.

Authors: M Kagimoto; J S Winter; K Kagimoto; E R Simpson; M R Waterman
Journal: Mol Endocrinol Date: 1988-06

6. The developmental changes in plasma adrenal androgens during infancy and adrenarche are associated with changing activities of adrenal microsomal 17-hydroxylase and 17,20-desmolase.

Authors: R J Schiebinger; B D Albertson; F G Cassorla; D W Bowyer; G W Geelhoed; G B Cutler; D L Loriaux
Journal: J Clin Invest Date: 1981-04 Impact factor: 14.808

7. Genetics and pathology of hereditary adrenal hyperplasia in the rabbit: a model for congenital lipoid adrenal hyperplasia.

Authors: R R Fox; D D Crary
Journal: J Hered Date: 1978 Jul-Aug Impact factor: 2.645

Steroid enzyme defects leading to male pseudohermaphroditism.

1. [Congenital adrenal hyperplasia due to blockade of 3-beta-hydroxysteroid dehydrogenase].

2. Persistent testicular delta5-isomerase-3beta-hydroxysteroid dehydrogenase (delta5-3beta-HSD) deficiency in the delta5-3beta-HSD form of congenital adrenal hyperplasia.

3. Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a stop codon in the N-terminal region of 17 alpha-hydroxylase cytochrome P-450.

4. [Congenital adrenal hyperplasia; 21-hydroxylase-deficiency combined with 17-desmolase-deficiency (author's transl)].

5. Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: molecular basis of one example of combined 17 alpha-hydroxylase/17,20 lyase deficiency.

6. The developmental changes in plasma adrenal androgens during infancy and adrenarche are associated with changing activities of adrenal microsomal 17-hydroxylase and 17,20-desmolase.

7. Genetics and pathology of hereditary adrenal hyperplasia in the rabbit: a model for congenital lipoid adrenal hyperplasia.

8. Assignment of the gene for adrenal P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase) to human chromosome 10.

9. Properties of an adrenal cytochrome P-450 (P-450SCC) for the side chain cleavage of cholesterol.

10. Two types of male pseudohermaphroditism due to 17, 20-desmolase deficiency.

Review 1. Intersex disorder associated with ambiguous genitalia.