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Journal Abstract Search

264 related items for PubMed ID: 6244328

  • 41. [Study of the transmission of the 21-hydroxylase deficiency through the hormonal screening and the HLA-typing (author's transl)].
    Bartolotta E, Migliori C, Gabrielli A, Oggiano N, Catassi C, Leone L.
    Pediatr Med Chir; 1981; 3(4):287-90. PubMed ID: 6283486
    [No Abstract] [Full Text] [Related]

  • 42.
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  • 43. Combined 21- and 11 beta-hydroxylase deficiency in familial congenital adrenal hyperplasia.
    Hurwitz A, Brautbar C, Milwidsky A, Vecsei P, Milewicz A, Navot D, Rösler A.
    J Clin Endocrinol Metab; 1985 Apr; 60(4):631-8. PubMed ID: 2982904
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  • 45. Heterozygotes for 17 alpha-hydroxylase deficiency can be detected with a short ACTH test.
    Wit JM, van Roermund HP, Oostdijk W, Benraad TJ, Thijssen JH, Boer P, Jansen M, Spit M, van den Brande JL.
    Clin Endocrinol (Oxf); 1988 Jun; 28(6):657-64. PubMed ID: 2855412
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  • 47. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review of current knowledge.
    Bacon GE, Kelch RP.
    J Endocrinol Invest; 1979 Jun; 2(1):93-100. PubMed ID: 385704
    [No Abstract] [Full Text] [Related]

  • 48. Dexamethasone preparation does not alter corticoid and androgen responses to adrenocorticotropin.
    Rosenfield RL, Helke J, Lucky AW.
    J Clin Endocrinol Metab; 1985 Mar; 60(3):585-9. PubMed ID: 2982902
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  • 50. [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]

  • 51. New studies of the 11 beta-hydroxylase and 18-hydroxylase enzymes in the hypertensive form of congenital adrenal hyperplasia.
    Levine LS, Rauh W, Gottesdiener K, Chow D, Gunczler P, Rapaport R, Pang S, Schneider B, New MI.
    J Clin Endocrinol Metab; 1980 Feb 15; 50(2):258-63. PubMed ID: 6243663
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  • 53. [Detection of heterozygosity in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the general population].
    Dumić M, Lukenda M, Plavsić V, Brkljacić L, Jovanović V, Kastelan A.
    Lijec Vjesn; 1990 Feb 15; 112(5-6):138-41. PubMed ID: 2172673
    [Abstract] [Full Text] [Related]

  • 54. Screening for non-classic 21-hydroxylase deficiency in an HLA-B14 positive population.
    Motta P, Airaghi L, Catania A, Mangone I, Orsatti A, Tenconi L, Cantalamessa L, Zanussi C.
    Acta Endocrinol (Copenh); 1987 Oct 15; 116(2):211-5. PubMed ID: 2821719
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  • 57. 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]

  • 58. Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Khandekar S, Lata V, Dash RJ.
    Indian J Med Res; 1990 Apr 07; 92():79-82. PubMed ID: 2164496
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  • 59.
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  • 60. Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency confirmed by HLA tissue typing.
    Zachmann M, Prader A.
    Acta Endocrinol (Copenh); 1979 Nov 07; 92(3):542-6. PubMed ID: 517053
    [Abstract] [Full Text] [Related]

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