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Journal Abstract Search

99 related items for PubMed ID: 6287777

  • 1. 17 alpha-hydroxylase deficiency syndrome associated with bilateral streak gonads and impaired development of Müllerian ducts derivatives. Report of a case.
    de Gennes JL, Jambart S, Turpin G, Elkik F, Roger M.
    Acta Endocrinol (Copenh); 1982 May; 100(1):68-76. PubMed ID: 6287777
    [Abstract] [Full Text] [Related]

  • 2. [Malignant arterial hypertension disclosing late congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency].
    Ribstein J, Sciolla JP, Barjon P, Sultan C, Forest M, de Peretti E.
    Arch Mal Coeur Vaiss; 1988 Jun; 81 Spec No():93-5. PubMed ID: 3142437
    [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 07; 313(19):1182-91. PubMed ID: 2932643
    [Abstract] [Full Text] [Related]

  • 4. Severe hypertension with absent secondary sex characteristics due to partial deficiency of steroid 17 alpha-hydroxylase activity.
    Fraser R, Brown JJ, Mason PA, Morton JJ, Lever AF, Robertson JI, Lee HA, Miller H.
    J Hum Hypertens; 1987 Jun 07; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 5. 17 alpha-hydroxylase deficiency in genetic females. A report of two cases.
    Nagamani M, Dinh TV.
    J Reprod Med; 1986 Aug 07; 31(8):734-8. PubMed ID: 3490570
    [Abstract] [Full Text] [Related]

  • 6. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency: diagnosis by gas chromatography--mass spectrometry.
    Burstein P, Marsh P, Fennessey P, Betz G.
    Obstet Gynecol; 1983 Mar 07; 61(3 Suppl):63S-68S. PubMed ID: 6296744
    [Abstract] [Full Text] [Related]

  • 7. Adrenocorticotropin-corticosterone relationship during dexamethasone therapy in 17 alpha-hydroxylase deficiency.
    Moreira AC, Leal AM, Castro M.
    Horm Metab Res; 1992 Jul 07; 24(7):339-41. PubMed ID: 1325404
    [Abstract] [Full Text] [Related]

  • 8. An autopsy case of 17 alpha-hydroxylase deficiency with malignant hypertension.
    Morimoto I, Maeda R, Izumi M, Ishimaru T, Nishimori I, Nagataki S.
    J Clin Endocrinol Metab; 1983 May 07; 56(5):915-9. PubMed ID: 6300176
    [Abstract] [Full Text] [Related]

  • 9. [Hirsutism and light forms of congenital adrenogenital syndrome with 21- and 11-beta hydroxylase defect].
    Zachmann M.
    Schweiz Med Wochenschr; 1986 Mar 29; 116(13):408-12. PubMed ID: 3486468
    [Abstract] [Full Text] [Related]

  • 10. 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 29; 98(2):267-73. PubMed ID: 6270940
    [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 29; 65(4):777-81. PubMed ID: 6966049
    [Abstract] [Full Text] [Related]

  • 12. 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 29; 46(2):236-46. PubMed ID: 312294
    [Abstract] [Full Text] [Related]

  • 13. [Primary amenorrhea and arterial hypertension in a case of 17 alpha-hydroxylase deficiency].
    Martin-Du Pan RC, Dahoun S, Stalberg A, Campana A.
    J Gynecol Obstet Biol Reprod (Paris); 1994 Feb 29; 23(2):137-40. PubMed ID: 8040569
    [Abstract] [Full Text] [Related]

  • 14. Control of aldosterone in 17 alpha-hydroxylase deficiency.
    Saruta T, Kondo K, Saito I, Nagahama S, Suzuki H, Konishi K, Matsuki S.
    Horm Res; 1980 Feb 29; 13(2):98-108. PubMed ID: 6262207
    [Abstract] [Full Text] [Related]

  • 15. 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 29; 56(4):697-701. PubMed ID: 6300162
    [Abstract] [Full Text] [Related]

  • 16. 17alpha-hydroxylase deficiency accompanied by adrenal myelolipoma.
    Nagai T, Imamura M, Honma M, Murakami M, Mori M.
    Intern Med; 2001 Sep 29; 40(9):920-3. PubMed ID: 11579957
    [Abstract] [Full Text] [Related]

  • 17. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency and hormonal profiles in the nuclear family.
    Rohmer V, Barbot N, Bertrand P, Nahoul K, Bigorgne JC, Forest MG.
    J Clin Endocrinol Metab; 1990 Aug 29; 71(2):523-9. PubMed ID: 2166072
    [Abstract] [Full Text] [Related]

  • 18. [Male pseudohermaphroditism caused by enzymatic deficiency of 17-alpha-hydroxylase. 1st case reported in Puerto Rico].
    Rosado A, Alegre M, Colón G.
    Bol Asoc Med P R; 1997 Aug 29; 89(10-12):197-9. PubMed ID: 9577056
    [Abstract] [Full Text] [Related]

  • 19. The unique patterns of plasma aldosterone and 18-hydroxycorticosterone concentrations in the 17 alpha-hydroxylase deficiency syndrome.
    Kater CE, Biglieri EG, Brust N, Chang B, Hirai J.
    J Clin Endocrinol Metab; 1982 Aug 29; 55(2):295-302. PubMed ID: 7045152
    [No Abstract] [Full Text] [Related]

  • 20. 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 29; 8(3):295-9. PubMed ID: 308800
    [Abstract] [Full Text] [Related]

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