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Journal Abstract Search

191 related items for PubMed ID: 6290362

  • 1. 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; 16(4):193-200. PubMed ID: 6290362
    [Abstract] [Full Text] [Related]

  • 2. Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Lee PA, Rosenwaks Z, Urban MD, Migeon CJ, Bias WD.
    J Clin Endocrinol Metab; 1982 Nov; 55(5):866-71. PubMed ID: 6288754
    [Abstract] [Full Text] [Related]

  • 3. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.
    Kohn B, Levine LS, Pollack MS, Pang S, Lorenzen F, Levy D, Lerner AJ, Rondanini GF, Dupont B, New MI.
    J Clin Endocrinol Metab; 1982 Nov; 55(5):817-27. PubMed ID: 6288753
    [Abstract] [Full Text] [Related]

  • 4. 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 Nov; 14(2):73-8. PubMed ID: 6268517
    [No Abstract] [Full Text] [Related]

  • 5. Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease.
    Chrousos GP, Loriaux DL, Mann DL, Cutler GB.
    Ann Intern Med; 1982 Feb; 96(2):143-8. PubMed ID: 6977282
    [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. 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]

  • 8. 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]

  • 9. The attenuated form of congenital adrenal hyperplasia as an allelic form of 21-hydroxylase deficiency.
    Migeon CJ, Rosenwaks Z, Lee PA, Urban MD, Bias WB.
    J Clin Endocrinol Metab; 1980 Sep; 51(3):647-9. PubMed ID: 6251108
    [Abstract] [Full Text] [Related]

  • 10. Late-onset type of 21-hydroxylase deficiency in childhood.
    Roitman A, Stivel M, Zamir R, Kaufman H, Pertzelan A, Laron Z.
    Isr J Med Sci; 1982 Jul; 18(7):763-8. PubMed ID: 6980865
    [Abstract] [Full Text] [Related]

  • 11. Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency.
    Speiser PW, New MI.
    J Clin Endocrinol Metab; 1987 Jan; 64(1):86-91. PubMed ID: 3023431
    [Abstract] [Full Text] [Related]

  • 12. [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]

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

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

  • 15. 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 13; 116(2):211-5. PubMed ID: 2821719
    [Abstract] [Full Text] [Related]

  • 16. 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 13; 60(4):631-8. PubMed ID: 2982904
    [Abstract] [Full Text] [Related]

  • 17. '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]

  • 18. 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]

  • 19. Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency.
    Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI.
    J Clin Endocrinol Metab; 1981 Dec 13; 53(6):1193-8. PubMed ID: 6271801
    [Abstract] [Full Text] [Related]

  • 20. 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 Dec 13; 200():243-55. PubMed ID: 3001775
    [No Abstract] [Full Text] [Related]

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