Literature DB >> 14250395

A NEW HEREDITARY DEFECT IN THE BIOSYNTHESIS OF ALDOSTERONE: URINARY C21-CORTICOSTEROID PATTERN IN THREE RELATED PATIENTS WITH A SALT-LOSING SYNDROME, SUGGESTING AN 18-OXIDATION DEFECT.

H K VISSER, W S COST.   

Abstract

Entities:  

Keywords:  17-HYDROXYCORTICOSTEROIDS; 17-KETOSTEROIDS; ADOLESCENCE; ALDOSTERONE; BIRTH ORDER; CONSANGUINITY; CORTICOTROPIN, THERAPEUTIC; DESOXYCORTICOSTERONE; GENETICS, HUMAN; HYPERKALEMIA; HYPONATREMIA; INFANT; METABOLISM, INBORN ERRORS; PATHOLOGY; SEX

Mesh：

Substances：

Year:  1964        PMID： 14250395     DOI： 10.1530/acta.0.0470589

Source DB:  PubMed          Journal:  Acta Endocrinol (Copenh)        ISSN： 0001-5598


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  12 in total

1.  Tubular Na, K-ATPase deficiency, the cause of the congenital renal salt-losing syndrome.

Authors:  J R Bierich; U Schmidt
Journal:  Eur J Pediatr       Date:  1976-01-02       Impact factor: 3.183

2.  Control of plasma aldosterone in diabetic patients with hyporeninemic hypoaldosteronism.

Authors:  U Kuhlmann; W Vetter; E Fischer; W Siegenthaler
Journal:  Klin Wochenschr       Date:  1978-03-01

3.  The biochemical phenotypes of two inborn errors in the biosynthesis of aldosterone.

Authors:  L Pascoe
Journal:  J Endocrinol Invest       Date:  1995 Jul-Aug       Impact factor: 4.256

4.  Salt-losing syndrome in 2 infants with defective 18-dehydrogenation in aldosterone biosynthesis.

Authors:  P J Milla; R Trompeter; M J Dillon; D Robins; C Shackleton
Journal:  Arch Dis Child       Date:  1977-07       Impact factor: 3.791

5.  Zone-specific regulation of two messenger RNAs for P450c11 in the adrenals of pregnant and nonpregnant rats.

Authors:  M P Malee; S H Mellon
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-01       Impact factor: 11.205

6.  Studies of the mechanism through which sodium depletion increases aldosterone biosynthesis in man.

Authors:  T Bledsoe; D P Island; G W Liddle
Journal:  J Clin Invest       Date:  1966-04       Impact factor: 14.808

Review 7.  The adrenal cortex in childhood.

Authors:  H K Visser
Journal:  Arch Dis Child       Date:  1966-02       Impact factor: 3.791

8.  Recurrent hyperkalaemia due to selective aldosterone deficiency: correction by angiotensin infusion.

Authors:  J J Brown; R H Chinn; R Fraser; A F Lever; J J Morton; J I Robertson; M Tree; M A Waite; D M Park
Journal:  Br Med J       Date:  1973-03-17

9.  Hypoaldosteronism in three sibs due to 18-dehydrogenase deficiency.

Authors:  W Hamilton; A E McCandless; J T Ireland; C E Gray
Journal:  Arch Dis Child       Date:  1976-08       Impact factor: 3.791

10.  Mutation THR-185 ILE is associated with corticosterone methyl oxidase deficiency type II.

Authors:  M Peter; K Bünger; J Sólyom; W G Sippell
Journal:  Eur J Pediatr       Date:  1998-05       Impact factor: 3.183
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