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Journal Abstract Search

103 related items for PubMed ID: 15387879

  • 1.
    ; . PubMed ID:
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  • 2. 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]

  • 3. 17-Hydroxyprogesterone deficiency as a cause of sexual infantilism and arterial hypertension: laboratory and molecular diagnosis--a case report.
    Benetti-Pinto CL, Vale D, Garmes H, Bedone A.
    Gynecol Endocrinol; 2007 Feb 21; 23(2):94-8. PubMed ID: 17454159
    [Abstract] [Full Text] [Related]

  • 4. 17α‑hydroxylase/17,20‑lyase deficiency in congenital adrenal hyperplasia: A case report.
    Xu S, Hu S, Yu X, Zhang M, Yang Y.
    Mol Med Rep; 2017 Jan 21; 15(1):339-344. PubMed ID: 27959413
    [Abstract] [Full Text] [Related]

  • 5. Pubertal delay, hypokalemia, and hypertension caused by a rare form of congenital adrenal hyperplasia.
    Olson CA, Crudo DF.
    J Pediatr Adolesc Gynecol; 2011 Apr 21; 24(2):e29-31. PubMed ID: 21190871
    [Abstract] [Full Text] [Related]

  • 6. [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]

  • 7.
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  • 8. Male pseudohermaphroditism as a cause of secondary hypertension: a case report.
    Aydin Z, Ozturk S, Gursu M, Uzun S, Karadag S, Kazancioglu R.
    Endocrine; 2010 Aug 10; 38(1):100-3. PubMed ID: 20960109
    [Abstract] [Full Text] [Related]

  • 9. Primary amenorrhea in two sisters: description of a Mexican family with 17α hydroxylase-17 lyase deficiency caused by arginine - stop mutation.
    Escamilla-Márquez MA, Garduño-Garcia Jde J, Ordóñez-Sanchez ML, Reza-Albarrán A, Tusie-Luna MT, Gómez Pérez FJ, Aguilar-Salinas CA.
    Gynecol Endocrinol; 2012 Sep 10; 28(9):733-5. PubMed ID: 22309630
    [Abstract] [Full Text] [Related]

  • 10. [Malignant arterial hypertension disclosing late congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency].
    Ribstein J, Sciolla JP, Barjon P, Sultan C, Forest M, de Peretti E.
    Arch Mal Coeur Vaiss; 1988 Jun 10; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 11. Congenital adrenal hyperplasia secondary to 17-hydroxylase deficiency. Two sisters with amenorrhea, hypokalemia, hypertension, and cystic ovaries.
    Mallin SR.
    Ann Intern Med; 1969 Jan 10; 70(1):69-75. PubMed ID: 4303304
    [No Abstract] [Full Text] [Related]

  • 12. A three-year-old with persistent hypokalemia.
    Shoemaker LR, Eaton BV, Buchino JJ.
    J Pediatr; 2007 Dec 10; 151(6):696-9. PubMed ID: 18035156
    [No Abstract] [Full Text] [Related]

  • 13. Seventeen alpha-hydroxylase deficiency.
    Wong SL, Shu SG, Tsai CR.
    J Formos Med Assoc; 2006 Feb 10; 105(2):177-81. PubMed ID: 16477341
    [Abstract] [Full Text] [Related]

  • 14. Congenital adrenal hyperplasia masquerading as periodic paralysis in an adolescent girl.
    Sathya A, Ganesan R, Kumar A.
    Singapore Med J; 2012 Jul 10; 53(7):e148-9. PubMed ID: 22815032
    [Abstract] [Full Text] [Related]

  • 15. [Primary amenorrhea and arterial hypertension in a case of 17 alpha-hydroxylase deficiency].
    Martin-Du Pan RC, Dahoun S, Stalberg A, Campana A.
    J Gynecol Obstet Biol Reprod (Paris); 1994 Jul 10; 23(2):137-40. PubMed ID: 8040569
    [Abstract] [Full Text] [Related]

  • 16. Hypokalaemic hypertension and 17-alpha-hydroxylase/17,20-lyase deficiency in a young girl: a case report.
    Yau HN, Lo WC, Yuen YP, Leung MT, Ng KL.
    Hong Kong Med J; 2024 Jun 10; 30(3):241-244. PubMed ID: 38825729
    [No Abstract] [Full Text] [Related]

  • 17. Case report: 17 alpha-hydroxylase/17,20-lyase deficiency: a rare cause of endocrine hypertension.
    Hermans C, de Plaen JF, de Nayer P, Maiter D.
    Am J Med Sci; 1996 Sep 10; 312(3):126-9. PubMed ID: 8783679
    [Abstract] [Full Text] [Related]

  • 18. A compound heterozygous mutation in the CYP17 (17alpha-hydroxylase/17,20-lyase) gene in a Chinese subject with congenital adrenal hyperplasia.
    Won GS, Chiu CY, Tso YC, Jenq SF, Cheng PS, Jap TS.
    Metabolism; 2007 Apr 10; 56(4):504-7. PubMed ID: 17379008
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Delayed puberty from partial 17-alpha hydroxylase enzyme deficiency.
    Croxson M, Ogilvie CM, Milsom S, Lewis J, Davidson J, Rumsby G.
    N Z Med J; 2012 May 25; 125(1355):71-4. PubMed ID: 22722218
    [Abstract] [Full Text] [Related]

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