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Journal Abstract Search

76 related items for PubMed ID: 6970788

  • 1. [A case of 17 alpha-hydroxylase deficiency with bone anomalies (author's transl)].
    Itatsu T, Naitoh K, Matsuda N, Matsui N.
    Nihon Naika Gakkai Zasshi; 1980 Aug 10; 69(8):960-6. PubMed ID: 6970788
    [No Abstract] [Full Text] [Related]

  • 2. [A case of 17 alpha-hydroxylase deficiency with long stature and epileptic cramps (author's transl)].
    Ono Y.
    Horumon To Rinsho; 1982 Apr 10; 30(4):353-7. PubMed ID: 6980065
    [No Abstract] [Full Text] [Related]

  • 3. Steroid secretion by granulosa cells isolated from a woman with 17 alpha-hydroxylase deficiency.
    Pariente C, Rabinovici J, Lunenfeld B, Rudak E, Dor J, Mashiach S, Levran D, Blankstein J, Geier A.
    J Clin Endocrinol Metab; 1990 Oct 10; 71(4):984-7. PubMed ID: 2401721
    [Abstract] [Full Text] [Related]

  • 4. [Micro-filter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay. Application for diagnosis of 21-hydroxylase deficiency (author's transl)].
    Shimozawa K, Tomita M, Nakagawa S, Saito Y, Sakurada N.
    Horumon To Rinsho; 1979 Sep 10; 27(9):1048-53. PubMed ID: 316748
    [No Abstract] [Full Text] [Related]

  • 5. Comments about the need for prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Migeon CJ.
    J Clin Endocrinol Metab; 1990 Apr 10; 70(4):836-7. PubMed ID: 2318944
    [No Abstract] [Full Text] [Related]

  • 6. Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Pang SY, Pollack MS, Marshall RN, Immken L.
    N Engl J Med; 1990 Jan 11; 322(2):111-5. PubMed ID: 2403652
    [No Abstract] [Full Text] [Related]

  • 7. [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 26; 10(47):3841-3. PubMed ID: 6977130
    [Abstract] [Full Text] [Related]

  • 8. Direct evidence for a functional block in 18 oxidation in a patient with 17 alpha hydroxylase deficiency.
    Rovner DR, Gordon DL, Swisher SN.
    Trans Assoc Am Physicians; 1978 Dec 26; 91():416-23. PubMed ID: 224555
    [No Abstract] [Full Text] [Related]

  • 9. [Neglected congenital adrenogenital syndrome (AGS) in an adult. A case report (21-hydroxylase deficiency) with a summary of the current status of therapy with reference to adulthood].
    Mackenroth T.
    Internist (Berl); 1986 Apr 26; 27(4):274-8. PubMed ID: 3519519
    [No Abstract] [Full Text] [Related]

  • 10. 17 alpha-hydroxylase deficiency in genetic females. A report of two cases.
    Nagamani M, Dinh TV.
    J Reprod Med; 1986 Aug 26; 31(8):734-8. PubMed ID: 3490570
    [Abstract] [Full Text] [Related]

  • 11. Testicular in vitro conversion of progesterone to testosterone and androstenedione in 17 alpha-hydroxylase deficiency.
    Salti IS, Hajj H, Dhib-Jalbut S.
    J Steroid Biochem; 1982 Aug 26; 17(2):155-7. PubMed ID: 6981031
    [Abstract] [Full Text] [Related]

  • 12. [Congenital virilization in a newborn girl of a mother with adrenogenital syndrome due to 21-hydroxylase deficiency].
    Ferrante L.
    Minerva Pediatr; 1976 Jun 23; 28(22):1443-4. PubMed ID: 986003
    [No Abstract] [Full Text] [Related]

  • 13. [A case of a simple virilizing form of 21-hydroxylase deficiency with schizophrenic symptoms, marked pigmentation and highly elevated plasma deoxycorticosterone].
    Suemaru S, Hashimoto K, Hattori T, Inoue H, Kageyama J, Ota Z.
    Nihon Naika Gakkai Zasshi; 1987 Jan 23; 76(1):112-7. PubMed ID: 3033104
    [No Abstract] [Full Text] [Related]

  • 14. [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 Jan 23; 44(8):637-40. PubMed ID: 2622705
    [Abstract] [Full Text] [Related]

  • 15. 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 23; 56(5):915-9. PubMed ID: 6300176
    [Abstract] [Full Text] [Related]

  • 16. [Late diagnosis hyperandrogenism due to adrenal enzyme deficiency (author's transl)].
    Hazard J, Guilhaume B, Requeda E, Perlemuter L, Cenac A, Bernheim R.
    Sem Hop; 1983 May 23; 56(47-68):1975-8. PubMed ID: 6256909
    [Abstract] [Full Text] [Related]

  • 17. Requirement of mineralocorticoid in congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.
    Hochberg Z, Benderly A, Kahana L, Zadik Z.
    J Clin Endocrinol Metab; 1986 Jul 23; 63(1):36-40. PubMed ID: 3011843
    [Abstract] [Full Text] [Related]

  • 18. [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 23; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 19. Delayed puberty from partial 17-alpha hydroxylase enzyme deficiency.
    Croxson M, Ogilvie CM, Milsom S, Lewis J, Davidson J, Rumsby G.
    N Z Med J; 2012 May 25; 125(1355):71-4. PubMed ID: 22722218
    [Abstract] [Full Text] [Related]

  • 20. First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency).
    Speiser PW, Laforgia N, Kato K, Pareira J, Khan R, Yang SY, Whorwood C, White PC, Elias S, Schriock E.
    J Clin Endocrinol Metab; 1990 Apr 25; 70(4):838-48. PubMed ID: 1969421
    [Abstract] [Full Text] [Related]

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