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

152 related items for PubMed ID: 6335215

  • 1. [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; 106(11-12):466-70. PubMed ID: 6335215
    [No Abstract] [Full Text] [Related]

  • 2. [21-Hydroxylase deficiency. Clinical expression of heterozygote carriers in a family].
    Colle M, Battin J.
    Arch Fr Pediatr; 1984; 41(7):483-5. PubMed ID: 6333857
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. [Hormonal profile and HLA typing of adult subjects from 7 families with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Bercovici JP, Tater D, Khoury S, Le Fur JM, Saleun JP, Nahoul K, Scholler R.
    Ann Endocrinol (Paris); 1982 Mar; 43(3):203-11. PubMed ID: 6984316
    [Abstract] [Full Text] [Related]

  • 6. [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 Mar; 112(5-6):138-41. PubMed ID: 2172673
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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]

  • 9. 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]

  • 10. HLA and hormonal studies in 5 patients with late-onset 21-hydroxylase deficiency syndrome (21OHDS).
    Scaroni C, Orlandini E, Venturi Pasini C, Gangemi M, Mantero F.
    J Endocrinol Invest; 1986 Feb; 9(1):65-70. PubMed ID: 3009598
    [Abstract] [Full Text] [Related]

  • 11. Ascertainment of 21-hydroxylase deficiency in individuals with HLA-B14 haplotype.
    Libber SM, Migeon CJ, Bias WB.
    J Clin Endocrinol Metab; 1985 Apr; 60(4):727-30. PubMed ID: 3871788
    [Abstract] [Full Text] [Related]

  • 12. [Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Couillin P.
    Presse Med; 1984 Apr 21; 13(17):1087-90. PubMed ID: 6232534
    [Abstract] [Full Text] [Related]

  • 13. 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 21; 116(2):211-5. PubMed ID: 2821719
    [Abstract] [Full Text] [Related]

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

  • 15. Hormonal profiles of heterozygotes in humans for 21-hydroxylase deficiency defined by HLA B typing.
    Bercovici JP, Khoury S, Le Fur JM, Saleun JP, Nahoul K, Scholler R.
    J Steroid Biochem; 1981 Oct 21; 14(10):1049-54. PubMed ID: 6975398
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. [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]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [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 15; 105(4):145-9. PubMed ID: 6602259
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.