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Journal Abstract Search

115 related items for PubMed ID: 24138383

  • 1. 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]

  • 2. 17-Alpha hydroxylase deficiency: an unusual cause of secondary amenorrhoea.
    Philip J, Anjali, Thomas N, Rajaratnam S, Seshadri MS.
    Aust N Z J Obstet Gynaecol; 2004 Oct 21; 44(5):477-8. PubMed ID: 15387879
    [No Abstract] [Full Text] [Related]

  • 3. A novel mutation in the N-terminal region of the CYP17A1 gene in a patient with 17 alpha-hydroxylase/17,20-lyase deficiency.
    Nuzzo V, Tauchmanova L, Brunetti-Pierri R, Zuccoli A, Lupoli G, Colao A, Brunetti-Pierri N.
    J Endocrinol Invest; 2009 Apr 21; 32(4):322-4. PubMed ID: 19636199
    [Abstract] [Full Text] [Related]

  • 4. 17-alpha-hydroxylase deficiency: a case report with clinical and molecular analysis.
    Li H, Qiao J, Guo H.
    Gynecol Endocrinol; 2010 Jul 21; 26(7):521-3. PubMed ID: 20170344
    [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. A report of congenital adrenal hyperplasia due to 17α-hydroxylase deficiency in two 46,XX sisters.
    Espinosa-Herrera F, Espín E, Tito-Álvarez AM, Beltrán LJ, Gómez-Correa D, Burgos G, Llamos A, Zurita C, Rojas S, Dueñas-Espín I, Cueva-Ludeña K, Salazar-Vega J, Pinto-Basto J.
    Gynecol Endocrinol; 2020 Jan 10; 36(1):24-29. PubMed ID: 31464148
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. P450c17 deficiency in Brazilian patients: biochemical diagnosis through progesterone levels confirmed by CYP17 genotyping.
    Martin RM, Lin CJ, Costa EM, de Oliveira ML, Carrilho A, Villar H, Longui CA, Mendonca BB.
    J Clin Endocrinol Metab; 2003 Dec 10; 88(12):5739-46. PubMed ID: 14671162
    [Abstract] [Full Text] [Related]

  • 10. [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 Dec 10; 23(2):137-40. PubMed ID: 8040569
    [Abstract] [Full Text] [Related]

  • 11. Hypokalemia: A Curious Case in a Young Woman.
    Hughes C, Koppanarayana S, Watson M, Nipah R, Laing I.
    J Appl Lab Med; 2020 Jul 01; 5(4):802-807. PubMed ID: 32395745
    [No Abstract] [Full Text] [Related]

  • 12. A Curious Case of Primary Amenorrhea.
    Burns AD, Taylor NF, Taylor DR, Bhake RC, Rahman F.
    Clin Chem; 2020 Sep 01; 66(9):1150-1154. PubMed ID: 32870997
    [No Abstract] [Full Text] [Related]

  • 13. 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 01; 30(3):241-244. PubMed ID: 38825729
    [No Abstract] [Full Text] [Related]

  • 14. Combined 17α-hydroxylase/17,20-lyase deficiency due to p.R96W mutation in the CYP17 gene in a Brazilian patient.
    Costenaro F, Rodrigues TC, Kater CE, Auchus RJ, Papari-Zareei M, Czepielewski MA.
    Arq Bras Endocrinol Metabol; 2010 Nov 01; 54(8):744-8. PubMed ID: 21340163
    [Abstract] [Full Text] [Related]

  • 15. 17α-HYDROXYLASE/17, 20-LYASE DEFICIENCY: CLINICAL AND MOLECULAR CHARACTERIZATION OF EIGHT CHINESE PATIENTS.
    Wu C, Fan S, Qian Y, Zhou Y, Jin J, Dai Z, Jiang L.
    Endocr Pract; 2017 May 01; 23(5):576-582. PubMed ID: 28225307
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 76(1):71-4. PubMed ID: 25613935
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 28(9):733-5. PubMed ID: 22309630
    [Abstract] [Full Text] [Related]

  • 18. Presentation, Diagnosis, and Follow-Up Characteristics of 17α-Hydroxylase Deficiency Cases with Exon 1-6 Deletion (Founder Mutation) in the CYP17A1Gene: 20-Year Single-Center Experience.
    Dundar I, Akinci A, Camtosun E, Ciftci N, Kayas L.
    Sex Dev; 2023 Sep 01; 17(1):43-50. PubMed ID: 36652930
    [Abstract] [Full Text] [Related]

  • 19. A young woman with hypogonadism, hypertension and hypokalaemia.
    Toh VK, Yung CH.
    Med J Malaysia; 2009 Sep 01; 64(3):242-3. PubMed ID: 20527279
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 38(1):100-3. PubMed ID: 20960109
    [Abstract] [Full Text] [Related]

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