123 related articles for article (PubMed ID: 308577)
1. Urinary steroid excretion in 17 alpha-hydroxylase deficiency.
Honour JW; Tourniaire J; Biglieri EG; Shackleton CH
J Steroid Biochem; 1978 Jun; 9(6):495-505. PubMed ID: 308577
[No Abstract] [Full Text] [Related]
2. Identification of new steroids in patients with 17 alpha-hydroxylase deficiency by capillary gas chromatography/mass spectrometry.
Blau N; Zachmann M; Kempken B; Staudenmann W; Möhr E; Curtius HC
Biomed Environ Mass Spectrom; 1987 Nov; 14(11):633-7. PubMed ID: 2962669
[TBL] [Abstract][Full Text] [Related]
3. Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
Peterson RE; Imperato-McGinley J; Gautier T; Shackleton C
N Engl J Med; 1985 Nov; 313(19):1182-91. PubMed ID: 2932643
[TBL] [Abstract][Full Text] [Related]
4. Pregnenolone, 17-OH-pregnenolone, and testosterone in plasma of patients with congenital adrenal hyperplasia.
McKenna TJ; Jennings AS; Liddle GW; Burr IM
J Clin Endocrinol Metab; 1976 May; 42(5):918-25. PubMed ID: 178685
[TBL] [Abstract][Full Text] [Related]
5. Evidence against significant 19-nor-deoxycorticosterone production in patients with 17 alpha-hydroxylase deficiency.
Shackleton CH
Clin Exp Hypertens A; 1982; 4(9-10):1529-39. PubMed ID: 6982794
[TBL] [Abstract][Full Text] [Related]
6. Effect of structure on the excretion of steroidal acids in human urine and their potential colorimetric assay as 17-oxogenic steroids.
Senciall IR; Riley C; Rahal S; Dey AC; Harding CA; Achary M
Clin Biochem; 1977 Feb; 10(1):32-7. PubMed ID: 837525
[TBL] [Abstract][Full Text] [Related]
7. Extraadrenal steroid 21-hydroxylase activity in a woman with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
Winkel CA; Casey ML; Worley RJ; Madden JD; MacDonald PC
J Clin Endocrinol Metab; 1983 Jan; 56(1):104-7. PubMed ID: 6600168
[TBL] [Abstract][Full Text] [Related]
8. Gynecomastia with congenital virilizing adrenal hyperplasia (11-beta-hydroxylase deficiency).
Maclaren NK; Migeon CJ; Raiti S
J Pediatr; 1975 Apr; 86(4):579-81. PubMed ID: 123956
[No Abstract] [Full Text] [Related]
9. 17 alpha-hydroxylase deficiency: mineralocorticoid hormone profiles in an affected family.
D'Armiento M; Reda G; Kater C; Shackleton CH; Biglieri EG
J Clin Endocrinol Metab; 1983 Apr; 56(4):697-701. PubMed ID: 6300162
[TBL] [Abstract][Full Text] [Related]
10. Metabolism of radiolabeled corticosterone in an adult with the 17 alpha-hydroxylase deficiency syndrome.
Shackleton CH; Biglieri EG; Roitman E; Honour JW
J Clin Endocrinol Metab; 1979 Jun; 48(6):976-82. PubMed ID: 312808
[TBL] [Abstract][Full Text] [Related]
11. Differences in metabolism of corticosterone by the newborn and adult human.
Honour JW; Shackleton HL
Biochem Soc Trans; 1978; 6(4):775-8. PubMed ID: 309411
[No Abstract] [Full Text] [Related]
12. Determination of steroid profiles in healthy and diseased states: identification and quantitation of a block of 17 alpha-hydroxylase.
Fennessey PV; Marsh PG; Orr ER; Burnstein P; Betz G
Clin Chim Acta; 1983 Mar; 129(1):3-11. PubMed ID: 6303630
[TBL] [Abstract][Full Text] [Related]
13. Combined 17 alpha- and 18-hydroxylase deficiency associated with complete male pseudohermaphroditism and hypoaldosteronism.
Waldhäusl W; Herkner K; Nowotny P; Bratusch-Marrain P
J Clin Endocrinol Metab; 1978 Feb; 46(2):236-46. PubMed ID: 312294
[TBL] [Abstract][Full Text] [Related]
14. [Late discovery of female pseudo-hermaphroditism by complete blockade 21-hydroxylase (author's transl)].
Heim J; Massart C; Lémée F; Amice-Chambon V
Nouv Presse Med; 1981 Dec; 10(47):3841-3. PubMed ID: 6977130
[TBL] [Abstract][Full Text] [Related]
15. [An analysis and identification of urinary steroids in normal people and patients with 21-hydroxylase deficiency and urinary excretion patterns].
Mizumoto T; Kondo S; Yamasaki S
Nihon Naibunpi Gakkai Zasshi; 1984 Feb; 60(2):131-46. PubMed ID: 6609847
[TBL] [Abstract][Full Text] [Related]
16. Steroid excretion in urine during suppression and stimulation of adrenals in the 17 alpha-hydroxylase deficiency syndrome.
Honour J; Millar G; Roitman E; Shackleton C
J Clin Endocrinol Metab; 1981 May; 52(5):1039-42. PubMed ID: 6262355
[TBL] [Abstract][Full Text] [Related]
17. Male pseudohermaphroditism due to 17-hydroxylase deficiency.
D'Alberton A; Reschini E; Motta T; Catania A
J Endocrinol Invest; 1989 Mar; 12(3):193-6. PubMed ID: 2786019
[TBL] [Abstract][Full Text] [Related]
18. Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.
Pang S; Levine LS; Lorenzen F; Chow D; Pollack M; Dupont B; Genel M; New MI
J Clin Endocrinol Metab; 1980 Mar; 50(3):586-9. PubMed ID: 6244328
[TBL] [Abstract][Full Text] [Related]
19. Primary adrenal insufficiency with hypertension. A case report on partial primary adrenal insufficiency and partial 11-beta-hydroxylase deficiency.
van Deijk WA; Blom PS; VD Vijver JC
Neth J Med; 1979; 22(6):191-4. PubMed ID: 316501
[No Abstract] [Full Text] [Related]
20. Two cases of 17 alpha-hydroxylase deficiency--one combined with complete gonadal agenesis.
Tvedegaard E; Frederiksen V; Olgaard K; Nielsen MD; Starup J
Acta Endocrinol (Copenh); 1981 Oct; 98(2):267-73. PubMed ID: 6270940
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
