These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

104 related items for PubMed ID: 6283486

  • 1. [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]

  • 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. 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]

  • 4. Late onset congenital adrenal hyperplasia in a Puerto Rican family: hormonal and HLA typing.
    Hernán Martínez J, Riestra JL.
    Bol Asoc Med P R; 1986 Nov; 78(11):472-6. PubMed ID: 3026413
    [No Abstract] [Full Text] [Related]

  • 5. 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 Nov; 200():243-55. PubMed ID: 3001775
    [No 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. Late onset adrenal hyperplasia (21-hydroxylase deficiency): 17-OH progesterone response to ACTH stimulation and HLA typing. A family study.
    Kauschansky A, Kaufman H, Zamir R, Elian E.
    Horm Res; 1981 Mar; 14(2):73-8. PubMed ID: 6268517
    [No Abstract] [Full Text] [Related]

  • 8. [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 Mar; 106(11-12):466-70. PubMed ID: 6335215
    [No Abstract] [Full Text] [Related]

  • 9. HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency.
    Stuckey MS, Boyne P, Macdonald WB, Christiansen FT, Houliston JB, Dawkins RL.
    Aust N Z J Med; 1980 Oct; 10(5):552-4. PubMed ID: 6258552
    [Abstract] [Full Text] [Related]

  • 10. Studies of the C-21 and C-19 steroids and HLA genotyping in siblings and parents of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Lorenzen F, Pang S, New M, Pollack M, Oberfield S, Dupont B, Chow D, Schneider B, Levine L.
    J Clin Endocrinol Metab; 1980 Mar; 50(3):572-7. PubMed ID: 6244326
    [No Abstract] [Full Text] [Related]

  • 11. Detection of heterozygote of 21-hydroxylase deficiency.
    Sobel DO, Gutai JP, Jones JC, Wagener DK, Smith W.
    Lancet; 1980 Jan 05; 1(8158):47. PubMed ID: 6101388
    [No Abstract] [Full Text] [Related]

  • 12. [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 05; 33(5):423-7. PubMed ID: 3729253
    [No Abstract] [Full Text] [Related]

  • 13. [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]

  • 14. 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]

  • 15. [21-Hydroxylase deficiency. Clinical expression of heterozygote carriers in a family].
    Colle M, Battin J.
    Arch Fr Pediatr; 1984 Jul 13; 41(7):483-5. PubMed ID: 6333857
    [Abstract] [Full Text] [Related]

  • 16. [Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype].
    Dumić M, Brkljacić L, Krzisnik C, Radica A, Tajić M, Kastelan A.
    Lijec Vjesn; 1983 Jul 13; 105(7-8):290-2. PubMed ID: 6605467
    [No Abstract] [Full Text] [Related]

  • 17. 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 13; 16(3):151-9. PubMed ID: 6286442
    [Abstract] [Full Text] [Related]

  • 18. HLA and congenital adrenal hyperplasia due to 11-hydroxylase deficiency.
    Glenthøj A, Nielsen MD, Starup J, Svejgaard A.
    Tissue Antigens; 1979 Aug 13; 14(2):181-2. PubMed ID: 494231
    [No Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis of congenital adrenal hyperplasia.
    Marcus ES, Holcombe JH, Tulchinsky D, Rich RR, Riccardi VM.
    Am J Med Genet; 1979 Aug 13; 4(2):201-4. PubMed ID: 517576
    [Abstract] [Full Text] [Related]

  • 20. [Genetic aspects in congenital adrenal hyperplasia (author's transl)].
    Zachmann M, Prader A.
    Schweiz Rundsch Med Prax; 1977 Jul 05; 66(27):809-13. PubMed ID: 896655
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.