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Journal Abstract Search

120 related items for PubMed ID: 6121730

  • 1. 17 alpha-hydroxylase deficiency in a genetic male and female sibling pair.
    Sills IN, MacGillivray MH, Amrhein JA, Migeon CJ, Peterson RE.
    Int J Gynaecol Obstet; 1981 Dec; 19(6):473-9. PubMed ID: 6121730
    [Abstract] [Full Text] [Related]

  • 2. Basic and clinical aspects of congenital adrenal hyperplasia.
    New MI.
    J Steroid Biochem; 1987 Dec; 27(1-3):1-7. PubMed ID: 3320531
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Hypertension due to 17alpha-hydroxylase deficiency.
    Wang C, Yeung RT, Coghlan JP, Oddie CJ, Scoggins BA, Stockigt JR.
    Aust N Z J Med; 1978 Jun; 8(3):295-9. PubMed ID: 308800
    [Abstract] [Full Text] [Related]

  • 5. Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease.
    Chrousos GP, Loriaux DL, Mann DL, Cutler GB.
    Ann Intern Med; 1982 Feb; 96(2):143-8. PubMed ID: 6977282
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Lee PA, Rosenwaks Z, Urban MD, Migeon CJ, Bias WD.
    J Clin Endocrinol Metab; 1982 Nov; 55(5):866-71. PubMed ID: 6288754
    [Abstract] [Full Text] [Related]

  • 8. [Adrenogenital syndrome with 21-hydroxylase deficiency].
    Dörr HG, Sippell WG.
    Monatsschr Kinderheilkd; 1993 Jul; 141(7):609-21. PubMed ID: 8413342
    [No Abstract] [Full Text] [Related]

  • 9. [Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Couillin P.
    Presse Med; 1984 Apr 21; 13(17):1087-90. PubMed ID: 6232534
    [Abstract] [Full Text] [Related]

  • 10. Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.
    Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield S, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI.
    J Clin Endocrinol Metab; 1980 Dec 21; 51(6):1316-24. PubMed ID: 6449518
    [Abstract] [Full Text] [Related]

  • 11. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
    Holcombe JH, Keenan BS, Nichols BL, Kirkland RT, Clayton GW.
    Pediatrics; 1980 Apr 21; 65(4):777-81. PubMed ID: 6966049
    [Abstract] [Full Text] [Related]

  • 12. [Familial congenital adrenal hyperplasia caused by 11 beta-hydroxylase. Failure of prevention of sexual ambiguity and prenatal diagnosis].
    Bouchard M, Forest MG, David M, Dechaud H, Juif JG.
    Pediatrie; 1989 Apr 21; 44(8):637-40. PubMed ID: 2622705
    [Abstract] [Full Text] [Related]

  • 13. Diagnosis of homozygosity and heterozygosity in congenital adrenal hyperplasia (CAH) and control of treatment.
    Knorr D, Bidlingmaier F, Höller W, Kuhnle U.
    J Steroid Biochem; 1983 Jul 21; 19(1B):645-53. PubMed ID: 6887889
    [Abstract] [Full Text] [Related]

  • 14. 17 alpha-hydroxylase deficiency in genetic females. A report of two cases.
    Nagamani M, Dinh TV.
    J Reprod Med; 1986 Aug 21; 31(8):734-8. PubMed ID: 3490570
    [Abstract] [Full Text] [Related]

  • 15. [Male pseudohermaphroditism caused by 17-alpha-hydroxylase deficiency. Personal case reports and a review of the literature].
    De Marinis L, Mancini A, Saporosi A, Calabrò F, Massari M, Moneta E, Menini E, Barbarino A.
    Minerva Ginecol; 1989 Jul 21; 41(7):337-42. PubMed ID: 2691923
    [Abstract] [Full Text] [Related]

  • 16. P450c17 deficiency in Brazilian patients: biochemical diagnosis through progesterone levels confirmed by CYP17 genotyping.
    Martin RM, Lin CJ, Costa EM, de Oliveira ML, Carrilho A, Villar H, Longui CA, Mendonca BB.
    J Clin Endocrinol Metab; 2003 Dec 21; 88(12):5739-46. PubMed ID: 14671162
    [Abstract] [Full Text] [Related]

  • 17. 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 07; 313(19):1182-91. PubMed ID: 2932643
    [Abstract] [Full Text] [Related]

  • 18. 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 07; 56(4):697-701. PubMed ID: 6300162
    [Abstract] [Full Text] [Related]

  • 19. Distinctive plasma aldosterone, 18-hydroxycorticosterone, and 18-hydroxydeoxycorticosterone profile in the 21-, 17 alpha-, and 11 beta-hydroxylase deficiency types of congenital adrenal hyperplasia.
    Kater CE, Biglieri EG.
    Am J Med; 1983 Jul 07; 75(1):43-8. PubMed ID: 6602548
    [Abstract] [Full Text] [Related]

  • 20. [Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis].
    Lambotte C.
    Rev Med Liege; 1986 Jan 15; 41(2):37-44. PubMed ID: 3006204
    [No Abstract] [Full Text] [Related]

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