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Journal Abstract Search

87 related items for PubMed ID: 930977

  • 21. 17-Alpha hydroxylase deficiency: an unusual cause of secondary amenorrhoea.
    Philip J, Anjali, Thomas N, Rajaratnam S, Seshadri MS.
    Aust N Z J Obstet Gynaecol; 2004 Oct; 44(5):477-8. PubMed ID: 15387879
    [No Abstract] [Full Text] [Related]

  • 22. [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 Oct; 23(2):137-40. PubMed ID: 8040569
    [Abstract] [Full Text] [Related]

  • 23. [Detection of heterozygotes in the classic type of congenital adrenal hyperplasia due to a 21-hydroxylase defect in our population as based on hormonal studies and HLA typing].
    Dumić M, Tajić M, Brkljacić L, Mardesić D, Radica A, Lukenda M, Gjurić G, Jovanović V, Plavsić V, Kastelan A.
    Lijec Vjesn; 1984 Oct; 106(11-12):466-70. PubMed ID: 6335215
    [No Abstract] [Full Text] [Related]

  • 24. Deletion of the long arm of the Y chromosome in an adolescent with short stature and hypogonadism.
    Botella-Carretero JI, Valero MA, Valcorba I, Ezquieta B, Alonso M, Barrio R.
    J Pediatr Endocrinol Metab; 2001 Jan; 14(1):103-6. PubMed ID: 11220698
    [Abstract] [Full Text] [Related]

  • 25. [17 alpha-hydroxylase deficiency].
    Kumagi R.
    Nihon Rinsho; 1977 Jan; 35 Suppl 1():1096-7. PubMed ID: 306453
    [No Abstract] [Full Text] [Related]

  • 26. [Virilization caused by 21-hydroxylase deficiency and axillary sweat gland hyperplasia].
    Jourdain JC, Le Lorier B, Mourier C, Ploussard JP, Roussel F.
    Ann Dermatol Venereol; 1988 Jan; 115(11):1136-8. PubMed ID: 3266452
    [No Abstract] [Full Text] [Related]

  • 27. [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]

  • 28. [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 29; 41(7):337-42. PubMed ID: 2691923
    [Abstract] [Full Text] [Related]

  • 29. XO-XX-XXX mosaicism with possible congenital adrenal hyperplasia.
    Edwards JA, Vance VK, Cohen MM, Schussler GC.
    J Clin Endocrinol Metab; 1970 May 29; 30(5):666-9. PubMed ID: 4315483
    [No Abstract] [Full Text] [Related]

  • 30. [Clinical polymorphism of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency and HLA phenotype].
    Dzenis IG, Brykova EK, Bakharev VA.
    Akush Ginekol (Mosk); 1990 Jan 29; (1):10-4. PubMed ID: 2353725
    [No Abstract] [Full Text] [Related]

  • 31. 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 29; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 32. [Clinical and genetic aspects of fertility disorders of chromosomal origin].
    Goebel KM, Hausmann L, Kaffarnik H.
    Cah Med; 1971 Feb 28; 12(3):191-7. PubMed ID: 5576654
    [No Abstract] [Full Text] [Related]

  • 33. 17 alpha-hydroxylase deficiency in genetic females. A report of two cases.
    Nagamani M, Dinh TV.
    J Reprod Med; 1986 Aug 28; 31(8):734-8. PubMed ID: 3490570
    [Abstract] [Full Text] [Related]

  • 34. Male pseudohermaphroditism due to 17-hydroxylase deficiency.
    D'Alberton A, Reschini E, Motta T, Catania A.
    J Endocrinol Invest; 1989 Mar 28; 12(3):193-6. PubMed ID: 2786019
    [Abstract] [Full Text] [Related]

  • 35. Adrenogenital syndrome (11-beta-hydroxylase deficiency) with hyperprolactinemia: reversal by glucocorticoid administration.
    Brautbar NN, Ben-David MM.
    Arch Intern Med; 1977 Nov 28; 137(11):1608-9. PubMed ID: 411440
    [No Abstract] [Full Text] [Related]

  • 36. [ON XX/XO MOSAICISM].
    NAGY S, ANTAL L, JAKUBECZ S.
    Acta Med Acad Sci Hung; 1964 Nov 28; 20():289-93. PubMed ID: 14239405
    [No Abstract] [Full Text] [Related]

  • 37. [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 28; 27(4):274-8. PubMed ID: 3519519
    [No Abstract] [Full Text] [Related]

  • 38. [New concepts in virilizing adrenal hyperplasia caused by 21-hydroxylase block].
    Cortínez A, Beas F, Devoto L, Henríquez C.
    Rev Chil Pediatr; 1985 Apr 28; 56(3):192-8. PubMed ID: 3879364
    [No Abstract] [Full Text] [Related]

  • 39. [Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency - different HLA genotypes in 2 brothers].
    Dumić M, Plavsić V, Brkljacić L, Sarnavka V, Mardesić D, Tajić M, Kastelan A.
    Lijec Vjesn; 1983 Apr 28; 105(4):145-9. PubMed ID: 6602259
    [No Abstract] [Full Text] [Related]

  • 40. Comments about the need for prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Migeon CJ.
    J Clin Endocrinol Metab; 1990 Apr 28; 70(4):836-7. PubMed ID: 2318944
    [No Abstract] [Full Text] [Related]

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