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Journal Abstract Search

118 related items for PubMed ID: 308800

  • 1. Hypertension due to 17alpha-hydroxylase deficiency.
    Wang C, Yeung RT, Coghlan JP, Oddie CJ, Scoggins BA, Stockigt JR.
    Aust N Z J Med; 1978 Jun; 8(3):295-9. PubMed ID: 308800
    [Abstract] [Full Text] [Related]

  • 2. Severe hypertension with absent secondary sex characteristics due to partial deficiency of steroid 17 alpha-hydroxylase activity.
    Fraser R, Brown JJ, Mason PA, Morton JJ, Lever AF, Robertson JI, Lee HA, Miller H.
    J Hum Hypertens; 1987 Jun; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 3. Partial deficiency of adrenal 11-hydroxylase. A possible cause of primary hypertension.
    de Simone G, Tommaselli AP, Rossi R, Valentino R, Lauria R, Scopacasa F, Lombardi G.
    Hypertension; 1985 Jun; 7(2):204-10. PubMed ID: 2984117
    [Abstract] [Full Text] [Related]

  • 4. Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
    Peterson RE, Imperato-McGinley J, Gautier T, Shackleton C.
    N Engl J Med; 1985 Nov 07; 313(19):1182-91. PubMed ID: 2932643
    [Abstract] [Full Text] [Related]

  • 5. 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 07; 60(4):631-8. PubMed ID: 2982904
    [Abstract] [Full Text] [Related]

  • 6. 19-Nor-corticosteroids in health, in hypertensive states in humans including 17 alpha-hydroxylase deficiency and in the spontaneously hypertensive rat (SHR).
    Melby JC, Dale SL, Holbrook M, Wilson TE, Griffing GT, Arison BH.
    Endocr Res; 1985 Apr 07; 10(3-4):591-607. PubMed ID: 6336061
    [Abstract] [Full Text] [Related]

  • 7. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
    Holcombe JH, Keenan BS, Nichols BL, Kirkland RT, Clayton GW.
    Pediatrics; 1980 Apr 07; 65(4):777-81. PubMed ID: 6966049
    [Abstract] [Full Text] [Related]

  • 8. New studies of the 11 beta-hydroxylase and 18-hydroxylase enzymes in the hypertensive form of congenital adrenal hyperplasia.
    Levine LS, Rauh W, Gottesdiener K, Chow D, Gunczler P, Rapaport R, Pang S, Schneider B, New MI.
    J Clin Endocrinol Metab; 1980 Feb 07; 50(2):258-63. PubMed ID: 6243663
    [Abstract] [Full Text] [Related]

  • 9. Male pseudohermaphroditism due to 17-hydroxylase deficiency.
    D'Alberton A, Reschini E, Motta T, Catania A.
    J Endocrinol Invest; 1989 Mar 07; 12(3):193-6. PubMed ID: 2786019
    [Abstract] [Full Text] [Related]

  • 10. A late 17α-hydroxylase deficiency diagnosis that leads to the discovery of a new CYP17 gene mutation.
    Guenego A, Morel Y, Ionesco O, Mallet D, Priou-Guesdon M.
    Ann Endocrinol (Paris); 2015 Feb 07; 76(1):71-4. PubMed ID: 25613935
    [Abstract] [Full Text] [Related]

  • 11. Plasma and urinary 19-nor-deoxycorticosterone in 17 alpha-hydroxylase deficiency syndrome.
    Griffing GT, Wilson TE, Holbrook MM, Dale SL, Jackson TK, Ullrich I, Melby JC.
    J Clin Endocrinol Metab; 1984 Nov 07; 59(5):1011-5. PubMed ID: 6332824
    [Abstract] [Full Text] [Related]

  • 12. Response of several adrenal steroids to ACTH stimulation in essential hypertension.
    Honda M, Nowaczynski W, Guthrie GP, Messerli FH, Tolis G, Kuchel O, Genest J.
    J Clin Endocrinol Metab; 1977 Feb 07; 44(2):264-72. PubMed ID: 190252
    [Abstract] [Full Text] [Related]

  • 13. A young woman with hypogonadism, hypertension and hypokalaemia.
    Toh VK, Yung CH.
    Med J Malaysia; 2009 Sep 07; 64(3):242-3. PubMed ID: 20527279
    [Abstract] [Full Text] [Related]

  • 14. Early diagnosis of 11 beta-hydroxylase deficiency in two siblings confirmed by analysis of a novel steroid metabolite in newborn urine.
    Hughes IA, Arisaka O, Perry LA, Honour JW.
    Acta Endocrinol (Copenh); 1986 Mar 07; 111(3):349-54. PubMed ID: 3515819
    [Abstract] [Full Text] [Related]

  • 15. Two cases of 17 alpha-hydroxylase deficiency--one combined with complete gonadal agenesis.
    Tvedegaard E, Frederiksen V, Olgaard K, Nielsen MD, Starup J.
    Acta Endocrinol (Copenh); 1981 Oct 07; 98(2):267-73. PubMed ID: 6270940
    [Abstract] [Full Text] [Related]

  • 16. 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 07; 100(1):68-76. PubMed ID: 6287777
    [Abstract] [Full Text] [Related]

  • 17. Combined 17 alpha- and 18-hydroxylase deficiency associated with complete male pseudohermaphroditism and hypoaldosteronism.
    Waldhäusl W, Herkner K, Nowotny P, Bratusch-Marrain P.
    J Clin Endocrinol Metab; 1978 Feb 07; 46(2):236-46. PubMed ID: 312294
    [Abstract] [Full Text] [Related]

  • 18. Diagnosis and natural history of 17-hydroxylase deficiency in a newborn male.
    Dean HJ, Shackleton CH, Winter JS.
    J Clin Endocrinol Metab; 1984 Sep 07; 59(3):513-20. PubMed ID: 6086702
    [Abstract] [Full Text] [Related]

  • 19. Extraadrenal steroid 21-hydroxylase activity in a woman with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Winkel CA, Casey ML, Worley RJ, Madden JD, MacDonald PC.
    J Clin Endocrinol Metab; 1983 Jan 07; 56(1):104-7. PubMed ID: 6600168
    [Abstract] [Full Text] [Related]

  • 20. A case of adrenogenital syndrome with aberrant 11beta-hydroxylation.
    Maschler I, Weidenfeld J, Muller A, Slavin S, Shaefer J, Chowers I, Finkelstein M.
    Acta Endocrinol (Copenh); 1977 Aug 07; 85(4):832-9. PubMed ID: 578062
    [Abstract] [Full Text] [Related]

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