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

258 related items for PubMed ID: 6251108

  • 21. 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]

  • 22. Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein.
    Donohoue PA, van Dop C, McLean RH, White PC, Jospe N, Migeon CJ.
    J Clin Endocrinol Metab; 1986 May; 62(5):995-1002. PubMed ID: 3007562
    [Abstract] [Full Text] [Related]

  • 23. Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus.
    O'Neill GJ, Dupont B, Pollack MS, Levine LS, New MI.
    Clin Immunol Immunopathol; 1982 May; 23(2):312-22. PubMed ID: 6980755
    [No Abstract] [Full Text] [Related]

  • 24. 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]

  • 25. 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]

  • 26. Adult-onset familial adrenal 21-hydroxylase deficiency.
    Blankstein J, Faiman C, Reyes FI, Schroeder ML, Winter JS.
    Am J Med; 1980 Mar; 68(3):441-8. PubMed ID: 6965821
    [Abstract] [Full Text] [Related]

  • 27. Genetics of congenital adrenal hyperplasia.
    New MI.
    Prog Clin Biol Res; 1985 Mar; 200():233-41. PubMed ID: 3878527
    [No Abstract] [Full Text] [Related]

  • 28. "Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia.
    New MI, Lorenzen F, Pang S, Gunczler P, Dupont B, Levine LS.
    J Clin Endocrinol Metab; 1979 Feb; 48(2):356-9. PubMed ID: 218988
    [Abstract] [Full Text] [Related]

  • 29. Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Layrisse Z, White C, Gunczler P, Gafaro Valera L, Arias S, Yunis EJ, Alper CA, Awdeh ZL.
    Immunogenetics; 1987 Feb; 25(2):99-103. PubMed ID: 3493216
    [Abstract] [Full Text] [Related]

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

  • 31. Adult manifestation of congenital adrenal hyperplasia due to incomplete 21-hydroxylase deficiency mimicking polycystic ovarian disease.
    Lobo RA, Goebelsmann U.
    Am J Obstet Gynecol; 1980 Nov 15; 138(6):720-6. PubMed ID: 6254362
    [Abstract] [Full Text] [Related]

  • 32. Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.
    Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield S, 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; 1980 Dec 15; 51(6):1316-24. PubMed ID: 6449518
    [Abstract] [Full Text] [Related]

  • 33. No linkage between HLA and congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency.
    Mantero F, Scaroni C, Pasini CV, Fagiolo U.
    N Engl J Med; 1980 Aug 28; 303(9):530. PubMed ID: 6967187
    [No Abstract] [Full Text] [Related]

  • 34. The 21-hydroxylase activity in the glomerulosa and fasciculata of the adrenal cortex in congenital adrenal hyperplasia.
    Kuhnle U, Chow D, Rapaport R, Pang S, Levine LS, New MI.
    J Clin Endocrinol Metab; 1981 Mar 28; 52(3):534-44. PubMed ID: 6257750
    [Abstract] [Full Text] [Related]

  • 35. Genotyping steroid 21-hydroxylase deficiency: hormonal reference data.
    New MI, Lorenzen F, Lerner AJ, Kohn B, Oberfield SE, Pollack MS, Dupont B, Stoner E, Levy DJ, Pang S, Levine LS.
    J Clin Endocrinol Metab; 1983 Aug 28; 57(2):320-6. PubMed ID: 6306039
    [Abstract] [Full Text] [Related]

  • 36. [HLA and congenital genital adrenal syndrome caused by 21-hydroxylase deficiency].
    Colabucci F, Saraca S, Rossodivita A, Giordano P, Luciani G.
    Minerva Pediatr; 1985 Sep 30; 37(18):696-7. PubMed ID: 3878454
    [No Abstract] [Full Text] [Related]

  • 37. [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 Sep 30; 105(7-8):290-2. PubMed ID: 6605467
    [No Abstract] [Full Text] [Related]

  • 38. HLA associations in 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) in France.
    Couillin P, Rappaport R, Kuttenn F, Hors J, Feingold J, Boué J, Boué A.
    Ann N Y Acad Sci; 1985 Sep 30; 458():41-5. PubMed ID: 3879129
    [No Abstract] [Full Text] [Related]

  • 39. The biochemical basis for genotyping 21-hydroxylase deficiency.
    New MI, Dupont B, Pollack MS, Levine LS.
    Hum Genet; 1981 Sep 30; 58(1):123-7. PubMed ID: 6269988
    [Abstract] [Full Text] [Related]

  • 40. '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 30; 109(3):386-92. PubMed ID: 2992207
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 13.