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Journal Abstract Search

114 related items for PubMed ID: 517053

  • 1. 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; 92(3):542-6. PubMed ID: 517053
    [Abstract] [Full Text] [Related]

  • 2. [Detection of heterozygous carriers of 21-hydroxylase deficiency-HLA typing and endocrinological study (author's transl)].
    Saito N, Kuribayashi T, Shimozawa K, Nakagawa S, Tomita M.
    Horumon To Rinsho; 1980 Jul; 28(7):767-72. PubMed ID: 7460327
    [No Abstract] [Full Text] [Related]

  • 3. [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 Jul; 3(4):287-90. PubMed ID: 6283486
    [No Abstract] [Full Text] [Related]

  • 4. Heterozygotes and cryptic patients in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency). HLA and glyoxalase I typing and hormonal studies.
    Petersen KE, Svejgaard A, Nielsen MD, Dissing J.
    Horm Res; 1982 Jul; 16(3):151-9. PubMed ID: 6286442
    [Abstract] [Full Text] [Related]

  • 5. Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Zachmann M, Prader A.
    Acta Endocrinol (Copenh); 1978 Mar; 87(3):557-65. PubMed ID: 580145
    [Abstract] [Full Text] [Related]

  • 6. Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S, Levine LS, Lorenzen F, Chow D, Pollack M, Dupont B, Genel M, New MI.
    J Clin Endocrinol Metab; 1980 Mar; 50(3):586-9. PubMed ID: 6244328
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis of congenital adrenal hyperplasia.
    Marcus ES, Holcombe JH, Tulchinsky D, Rich RR, Riccardi VM.
    Am J Med Genet; 1979 Mar; 4(2):201-4. PubMed ID: 517576
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  • 10. 21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patients.
    Livieri C, Belvedere M, Martinetti M, Beluffi G, Fiori P, Cogliati CR, Goffredo V, Lorini R, Severi F.
    Prog Clin Biol Res; 1985 Mar; 200():243-55. PubMed ID: 3001775
    [No Abstract] [Full Text] [Related]

  • 11. [A genetic and hormonal study of 5 patients with the nonclassical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Velasco FJ, Picó AM, Muñoz C, Mauri M, de la Sen ML.
    Med Clin (Barc); 1992 Jun 13; 99(3):81-6. PubMed ID: 1321317
    [Abstract] [Full Text] [Related]

  • 12. Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.
    Laron Z, Pollack MS, Zamir R, Roitman A, Dickerman Z, Levine LS, Lorenzen F, O'Neill GJ, Pang S, New MI, Dupont B.
    Hum Immunol; 1980 Jul 13; 1(1):55-66. PubMed ID: 6266983
    [No Abstract] [Full Text] [Related]

  • 13. [21-hydroxylase deficiency: a case in a newborn revealing a maternal forme tardive].
    Simonin G, Palix C, Roulier R, Coignet J.
    Ann Pediatr (Paris); 1986 May 13; 33(5):423-7. PubMed ID: 3729253
    [No Abstract] [Full Text] [Related]

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  • 15. Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations.
    Chrousos GP, Loriaux DL, Mann D, Cutler GB.
    Horm Res; 1982 May 13; 16(4):193-200. PubMed ID: 6290362
    [Abstract] [Full Text] [Related]

  • 16. 'Cryptic' form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in the Yugoslav population.
    Dumić M, Brkljacić L, Mardesić D, Plavsić V, Lukenda M, Kastelan A.
    Acta Endocrinol (Copenh); 1985 Jul 13; 109(3):386-92. PubMed ID: 2992207
    [Abstract] [Full Text] [Related]

  • 17. [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 Jul 13; 112(5-6):138-41. PubMed ID: 2172673
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  • 19. Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing.
    Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon M, Owens RP, Merkatz IR, Nitowsky BM, Sachs G, Dupont B.
    Lancet; 1979 May 26; 1(8126):1107-8. PubMed ID: 86832
    [Abstract] [Full Text] [Related]

  • 20. HLA and congenital adrenal hyperplasia due to 11-hydroxylase deficiency.
    Glenthøj A, Nielsen MD, Starup J, Svejgaard A.
    Tissue Antigens; 1979 Aug 26; 14(2):181-2. PubMed ID: 494231
    [No Abstract] [Full Text] [Related]

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