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Journal Abstract Search

105 related items for PubMed ID: 7023391

  • 1. Familial X-linked adrenocortical hypoplasia association with androgenic precocity.
    Wittenberg DF.
    Arch Dis Child; 1981 Aug; 56(8):633-6. PubMed ID: 7023391
    [Abstract] [Full Text] [Related]

  • 2. Familial cytomegalic adrenocortical hypoplasia: an X-linked syndrome of pubertal failure.
    Hay ID, Smail PJ, Forsyth CC.
    Arch Dis Child; 1981 Sep; 56(9):715-21. PubMed ID: 7197507
    [Abstract] [Full Text] [Related]

  • 3. Gonadotropin-independent familial sexual precocity with premature Leydig and germinal cell maturation (familial testotoxicosis): effects of a potent luteinizing hormone-releasing factor agonist and medroxyprogesterone acetate therapy in four cases.
    Rosenthal SM, Grumbach MM, Kaplan SL.
    J Clin Endocrinol Metab; 1983 Sep; 57(3):571-9. PubMed ID: 6223935
    [Abstract] [Full Text] [Related]

  • 4. Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndrome.
    Burke BA, Wick MR, King R, Thompson T, Hansen J, Darrae BT, Francke U, Seltzer WK, McCabe ER, Scheithauer BW.
    Am J Med Genet; 1988 Sep; 31(1):75-97. PubMed ID: 2906226
    [Abstract] [Full Text] [Related]

  • 5. Normal postnatal androgen production and action in isolated micropenis and isolated hypospadias.
    Evans BA, Williams DM, Hughes IA.
    Arch Dis Child; 1991 Sep; 66(9):1033-6. PubMed ID: 1929508
    [Abstract] [Full Text] [Related]

  • 6. Familial adrenocortical hypoplasia with early clinical and biochemical signs of mineralocorticoid deficiency (hypoaldosteronism).
    Petersen KE, Tygstrup I, Thamdrup E.
    Acta Endocrinol (Copenh); 1977 Mar; 84(3):605-19. PubMed ID: 576534
    [Abstract] [Full Text] [Related]

  • 7. X-linked adrenal hypoplasia congenita: a mutation in DAX1 expands the phenotypic spectrum in males and females.
    Seminara SB, Achermann JC, Genel M, Jameson JL, Crowley WF.
    J Clin Endocrinol Metab; 1999 Dec; 84(12):4501-9. PubMed ID: 10599709
    [Abstract] [Full Text] [Related]

  • 8. X-linked congenital adrenal hypoplasia. A study of five generations of a Greenlandic Family.
    Petersen KE, Bille T, Jacobsen BB, Iversen T.
    Acta Paediatr Scand; 1982 Nov; 71(6):947-51. PubMed ID: 6891556
    [Abstract] [Full Text] [Related]

  • 9. Use of a potent, long acting agonist of gonadotropin-releasing hormone in the treatment of precocious puberty.
    Boepple PA, Mansfield MJ, Wierman ME, Rudlin CR, Bode HH, Crigler JF, Crawford JD, Crowley WF.
    Endocr Rev; 1986 Feb; 7(1):24-33. PubMed ID: 2937629
    [Abstract] [Full Text] [Related]

  • 10. IMAGe association: additional clinical features and evidence for recessive autosomal inheritance.
    Lienhardt A, Mas JC, Kalifa G, Chaussain JL, Tauber M.
    Horm Res; 2002 Feb; 57 Suppl 2():71-8. PubMed ID: 12065932
    [Abstract] [Full Text] [Related]

  • 11. Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.
    Wilson JD, Harrod MJ, Goldstein JL, Hemsell DL, MacDonald PC.
    N Engl J Med; 1974 May 16; 290(20):1097-103. PubMed ID: 4821173
    [No Abstract] [Full Text] [Related]

  • 12. Rudimentary testes syndrome revisited.
    Acquafredda A, Vassal J, Job JC.
    Pediatrics; 1987 Aug 16; 80(2):209-14. PubMed ID: 3112728
    [Abstract] [Full Text] [Related]

  • 13. [Plasma androgens and maturation of the hypothalamo-pituitary-gonadal axis in infants and children (author's transl)].
    Forest MG.
    Padiatr Padol Suppl; 1977 Aug 16; (5):13-28. PubMed ID: 917573
    [Abstract] [Full Text] [Related]

  • 14. X-linked congenital adrenal hypoplasia: proposal pathogenesis.
    Preeyasombat C, Sriphrapradang A, Chaubtam L.
    J Med Assoc Thai; 1989 Jan 16; 72 Suppl 1():164-73. PubMed ID: 2732638
    [Abstract] [Full Text] [Related]

  • 15. Testicular enlargement in a pre-pubertal boy with adrenocortical tumour.
    Korwutthikulrangsri M, Wattanatranon D, Teeraratkul S, Wijarn P, Mahachoklertwattana P, Poomthavorn P.
    Paediatr Int Child Health; 2018 Feb 16; 38(1):66-68. PubMed ID: 28112592
    [Abstract] [Full Text] [Related]

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    [No Abstract] [Full Text] [Related]

  • 17. Mode of inheritance in familial cases of primary gonadotropic deficiency.
    Chaussain JL, Toublanc JE, Feingold J, Naud C, Vassal J, Job JC.
    Horm Res; 1988 Feb 16; 29(5-6):202-6. PubMed ID: 3146543
    [Abstract] [Full Text] [Related]

  • 18. NR0B1 Frameshift Mutation in a Boy with Idiopathic Central Precocious Puberty.
    Shima H, Yatsuga S, Nakamura A, Sano S, Sasaki T, Katsumata N, Suzuki E, Hata K, Nakabayashi K, Momozawa Y, Kubo M, Okamura K, Kure S, Matsubara Y, Ogata T, Narumi S, Fukami M.
    Sex Dev; 2016 Feb 16; 10(4):205-209. PubMed ID: 27648561
    [Abstract] [Full Text] [Related]

  • 19. Adrenal hypoplasia congenita with hypogonadotropic hypogonadism: evidence that DAX-1 mutations lead to combined hypothalmic and pituitary defects in gonadotropin production.
    Habiby RL, Boepple P, Nachtigall L, Sluss PM, Crowley WF, Jameson JL.
    J Clin Invest; 1996 Aug 15; 98(4):1055-62. PubMed ID: 8770879
    [Abstract] [Full Text] [Related]

  • 20. Testicular leydig cell hyperplasia as a cause of familial sexual precocity.
    Schedewie HK, Reiter EO, Beitins IZ, Seyed S, Wooten VD, Jimenez JF, Aiman EJ, DeVane GW, Redman JF, Elders MJ.
    J Clin Endocrinol Metab; 1981 Feb 15; 52(2):271-8. PubMed ID: 6780588
    [Abstract] [Full Text] [Related]

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