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Journal Abstract Search

96 related items for PubMed ID: 20527279

  • 21. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
    Holcombe JH, Keenan BS, Nichols BL, Kirkland RT, Clayton GW.
    Pediatrics; 1980 Apr; 65(4):777-81. PubMed ID: 6966049
    [Abstract] [Full Text] [Related]

  • 22. 17 alpha-hydroxylase deficiency syndrome associated with bilateral streak gonads and impaired development of Müllerian ducts derivatives. Report of a case.
    de Gennes JL, Jambart S, Turpin G, Elkik F, Roger M.
    Acta Endocrinol (Copenh); 1982 May; 100(1):68-76. PubMed ID: 6287777
    [Abstract] [Full Text] [Related]

  • 23. Hypertension in a neonate with 11 beta-hydroxylase deficiency.
    Mimouni M, Kaufman H, Roitman A, Morag C, Sadan N.
    Eur J Pediatr; 1985 Jan; 143(3):231-3. PubMed ID: 3872797
    [Abstract] [Full Text] [Related]

  • 24. [Problems posed by the association of hemophilia A and congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Boutte P, Madar H, d'Ollone M, Ferracci JP, Bebin B, Lambert JC, Sebag F.
    Pediatrie; 1986 Jan; 41(7):559-64. PubMed ID: 3493478
    [Abstract] [Full Text] [Related]

  • 25. [Neglected congenital adrenogenital syndrome (AGS) in an adult. A case report (21-hydroxylase deficiency) with a summary of the current status of therapy with reference to adulthood].
    Mackenroth T.
    Internist (Berl); 1986 Apr; 27(4):274-8. PubMed ID: 3519519
    [No Abstract] [Full Text] [Related]

  • 26. Congenital adrenal hyperplasia masquerading as periodic paralysis in an adolescent girl.
    Sathya A, Ganesan R, Kumar A.
    Singapore Med J; 2012 Jul; 53(7):e148-9. PubMed ID: 22815032
    [Abstract] [Full Text] [Related]

  • 27. [The deficiency of 17-hydroxylase: a cause of growth and puberty retardation in the girl. One case].
    Feit JP, David L, Patricot MC, Macabéo V, Lebacq E, François R.
    Arch Fr Pediatr; 1978 Apr; 35(4):395-405. PubMed ID: 308359
    [Abstract] [Full Text] [Related]

  • 28. Prenatal diagnosis and management of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Passarge E.
    Indian J Pediatr; 1988 Apr; 55(4):472-5. PubMed ID: 3262582
    [No Abstract] [Full Text] [Related]

  • 29. [Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups].
    Cruz-Marin F, Raffoux C, Gilgenkrantz S, Janot C, Streiff F, Pierson M.
    J Genet Hum; 1981 Mar; 29(1):103-13. PubMed ID: 6977617
    [No Abstract] [Full Text] [Related]

  • 30. [11Beta-hydroxylase deficiency].
    Narumi S, Hasegawa T.
    Nihon Rinsho; 2006 May 28; Suppl 1():699-701. PubMed ID: 16776252
    [No Abstract] [Full Text] [Related]

  • 31. 17-alpha-hydroxylase deficiency: a case report with clinical and molecular analysis.
    Li H, Qiao J, Guo H.
    Gynecol Endocrinol; 2010 Jul 28; 26(7):521-3. PubMed ID: 20170344
    [Abstract] [Full Text] [Related]

  • 32. Primary amenorrhoea with hypertension: undiagnosed 17-α-hydroxylase deficiency.
    Britten FL, Ulett KB, Duncan EL, Perry-Keene DA.
    Med J Aust; 2013 Oct 21; 199(8):556-8. PubMed ID: 24138383
    [No Abstract] [Full Text] [Related]

  • 33. [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 21; 105(4):145-9. PubMed ID: 6602259
    [No Abstract] [Full Text] [Related]

  • 34. [17 alpha-hydroxylase deficiency and 5 alpha-reductase deficiency].
    Yoshida H, Shimizu N.
    Nihon Rinsho; 1979 Jun 10; 37(6):1253-9. PubMed ID: 384051
    [No Abstract] [Full Text] [Related]

  • 35. Hypokalemic myopathy associated with 17 alpha-hydroxylase deficiency: a case report.
    Yazaki K, Kuribayashi T, Yamamura Y, Kurihara T, Araki S.
    Neurology; 1982 Jan 10; 32(1):94-7. PubMed ID: 6976525
    [Abstract] [Full Text] [Related]

  • 36. Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescents.
    Emans SJ, Grace E, Fleischnick E, Mansfield MJ, Crigler JF.
    Pediatrics; 1983 Nov 10; 72(5):690-5. PubMed ID: 6314235
    [Abstract] [Full Text] [Related]

  • 37. Pubertal delay, hypokalemia, and hypertension caused by a rare form of congenital adrenal hyperplasia.
    Olson CA, Crudo DF.
    J Pediatr Adolesc Gynecol; 2011 Apr 10; 24(2):e29-31. PubMed ID: 21190871
    [Abstract] [Full Text] [Related]

  • 38. Occurrence of male phenotype in genotypic females with congenital virilizing adrenal hyperplasia.
    Chan-Cua S, Freidenberg G, Jones KL.
    Am J Med Genet; 1989 Nov 10; 34(3):406-12. PubMed ID: 2574534
    [Abstract] [Full Text] [Related]

  • 39. Anaesthesia for a girl with severe hypertension due to 11 beta-hydroxylase deficiency.
    Okamoto T, Minami K.
    Anaesth Intensive Care; 2003 Oct 10; 31(5):596. PubMed ID: 14601294
    [No Abstract] [Full Text] [Related]

  • 40. Male pseudohermaphroditism due to 17-hydroxylase deficiency.
    D'Alberton A, Reschini E, Motta T, Catania A.
    J Endocrinol Invest; 1989 Mar 10; 12(3):193-6. PubMed ID: 2786019
    [Abstract] [Full Text] [Related]

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