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Journal Abstract Search

148 related items for PubMed ID: 2786019

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

  • 2. 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; 46(2):236-46. PubMed ID: 312294
    [Abstract] [Full Text] [Related]

  • 3. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.
    Yanase E, Nagai T, Kato M, Morimoto S.
    Jpn J Med; 1982 Apr; 21(2):128-34. PubMed ID: 6750188
    [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. An autopsy case of 17 alpha-hydroxylase deficiency with malignant hypertension.
    Morimoto I, Maeda R, Izumi M, Ishimaru T, Nishimori I, Nagataki S.
    J Clin Endocrinol Metab; 1983 May 07; 56(5):915-9. PubMed ID: 6300176
    [Abstract] [Full Text] [Related]

  • 6. 17 alpha-hydroxylase deficiency in genetic females. A report of two cases.
    Nagamani M, Dinh TV.
    J Reprod Med; 1986 Aug 07; 31(8):734-8. PubMed ID: 3490570
    [Abstract] [Full Text] [Related]

  • 7. [Deficiency of 17 alpha-hydroxylase. Presentation of 3 new cases].
    Gómez Sáez JM, Romero González R, Soler Ramón J, Bonnin Lafuenta R, Porta Martí M.
    Med Clin (Barc); 1984 Mar 10; 82(9):407-9. PubMed ID: 6609291
    [No Abstract] [Full Text] [Related]

  • 8. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency: diagnosis by gas chromatography--mass spectrometry.
    Burstein P, Marsh P, Fennessey P, Betz G.
    Obstet Gynecol; 1983 Mar 10; 61(3 Suppl):63S-68S. PubMed ID: 6296744
    [Abstract] [Full Text] [Related]

  • 9. [Male pseudohermaphroditism caused by enzymatic deficiency of 17-alpha-hydroxylase. 1st case reported in Puerto Rico].
    Rosado A, Alegre M, Colón G.
    Bol Asoc Med P R; 1997 Mar 10; 89(10-12):197-9. PubMed ID: 9577056
    [Abstract] [Full Text] [Related]

  • 10. 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 10; 8(3):295-9. PubMed ID: 308800
    [Abstract] [Full Text] [Related]

  • 11. [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]

  • 12. [Male pseudohermaphroditism caused by 17-alpha-hydroxylase deficiency. Personal case reports and a review of the literature].
    De Marinis L, Mancini A, Saporosi A, Calabrò F, Massari M, Moneta E, Menini E, Barbarino A.
    Minerva Ginecol; 1989 Jul 10; 41(7):337-42. PubMed ID: 2691923
    [Abstract] [Full Text] [Related]

  • 13. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency and hormonal profiles in the nuclear family.
    Rohmer V, Barbot N, Bertrand P, Nahoul K, Bigorgne JC, Forest MG.
    J Clin Endocrinol Metab; 1990 Aug 10; 71(2):523-9. PubMed ID: 2166072
    [Abstract] [Full Text] [Related]

  • 14. 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 10; 76(1):71-4. PubMed ID: 25613935
    [Abstract] [Full Text] [Related]

  • 15. A case of 17 alpha-hydroxylase deficiency syndrome associated with right adrenal tumor.
    Ogawa K, Hara A, Tanabe S, Tamori S, Yoshida H, Pak CH, Matsunaga M, Kawai C, Dodo H, Tanimura H.
    Clin Exp Hypertens A; 1984 Feb 10; 6(4):863-77. PubMed ID: 6609788
    [Abstract] [Full Text] [Related]

  • 16. Dexamethasone-suppressible hypercorticosteronism in two 46,XX subjects with ambiguous genitalia and ovarian cysts. Partial defect of 17 alpha-hydroxylase or 17-20-desmolase.
    Roger M, Merceron RE, Girard F, Canlorbe P, Dehennin L, Konopka P, Seneze J, Toublanc JE.
    Horm Res; 1982 Feb 10; 16(1):23-31. PubMed ID: 6279481
    [Abstract] [Full Text] [Related]

  • 17. Hypergonadotrophic male pseudohermaphroditism due to complete 17-alpha-hyroxylase deficiency.
    Waldhäusl WK, Herkner K, Bratusch-Marrain P, Haydl H, Nowotny P.
    Padiatr Padol Suppl; 1977 Feb 10; (5):103-7. PubMed ID: 917571
    [Abstract] [Full Text] [Related]

  • 18. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 Feb 10; 52(11-12):447-54. PubMed ID: 10748766
    [Abstract] [Full Text] [Related]

  • 19. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.
    New MI.
    J Clin Invest; 1970 Oct 10; 49(10):1930-41. PubMed ID: 5456802
    [Abstract] [Full Text] [Related]

  • 20. A case of 16-ene-synthetase deficiency in male pseudohermaphroditism due to combined 17 alpha-hydroxylase/17,20-lyase deficiency.
    Oei SG, Derksen J, Weusten JJ, Lentjes EG, Helmerhorst FM.
    Eur J Endocrinol; 1995 Mar 10; 132(3):281-5. PubMed ID: 7889174
    [Abstract] [Full Text] [Related]

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