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Journal Abstract Search

108 related items for PubMed ID: 38825729

  • 1. 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; 30(3):241-244. PubMed ID: 38825729
    [No Abstract] [Full Text] [Related]

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

  • 3. 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]

  • 4. 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 21; 36(1):24-29. PubMed ID: 31464148
    [Abstract] [Full Text] [Related]

  • 5. Seventeen alpha-hydroxylase deficiency.
    Wong SL, Shu SG, Tsai CR.
    J Formos Med Assoc; 2006 Feb 21; 105(2):177-81. PubMed ID: 16477341
    [Abstract] [Full Text] [Related]

  • 6. 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 21; 54(8):744-8. PubMed ID: 21340163
    [Abstract] [Full Text] [Related]

  • 7. Fertility in patients with genetic deficiencies of cytochrome P450c17 (CYP17A1): combined 17-hydroxylase/17,20-lyase deficiency and isolated 17,20-lyase deficiency.
    Marsh CA, Auchus RJ.
    Fertil Steril; 2014 Feb 21; 101(2):317-22. PubMed ID: 24485502
    [Abstract] [Full Text] [Related]

  • 8. A novel compound heterozygous mutation in the CYP17A1 gene in a patient with 17α-hydroxylase/17,20-lyase deficiency.
    Sun M, Yan X, Feng A, Wu X, Ye E, Wu H, Lu X, Yang H.
    Discov Med; 2017 Nov 21; 24(133):175-182. PubMed ID: 29278670
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Genetic defect of a combined 17 α-hydroxylase/17,20-lyase deficiency patient with adrenal crisis.
    Zhang Y, Zhang X, Wang Y, Hua K, Ding J.
    Gynecol Endocrinol; 2018 Jun 21; 34(6):540-544. PubMed ID: 29345162
    [Abstract] [Full Text] [Related]

  • 11. 17-Hydroxylase/17,20 lyase deficiency diagnosed during childhood.
    Wolthers OD, Rumsby G, Techatraisak K, Honour JW, Hindmarsh PC.
    Horm Res; 2002 Jun 21; 57(3-4):133-6. PubMed ID: 12006710
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Disorders of steroid 17 alpha-hydroxylase deficiency.
    Kater CE, Biglieri EG.
    Endocrinol Metab Clin North Am; 1994 Jun 21; 23(2):341-57. PubMed ID: 8070426
    [Abstract] [Full Text] [Related]

  • 14. 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 21; 38(1):100-3. PubMed ID: 20960109
    [Abstract] [Full Text] [Related]

  • 15. Congenital adrenal hyperplasia secondary to 17-hydroxylase deficiency. Two sisters with amenorrhea, hypokalemia, hypertension, and cystic ovaries.
    Mallin SR.
    Ann Intern Med; 1969 Jan 21; 70(1):69-75. PubMed ID: 4303304
    [No Abstract] [Full Text] [Related]

  • 16. 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 21; 28(9):733-5. PubMed ID: 22309630
    [Abstract] [Full Text] [Related]

  • 17. The Glu331del mutation in the CYP17A1 gene causes atypical congenital adrenal hyperplasia in a 46,XX female.
    Lanzolla G, Vancieri G, Lanciotti S, Sangiuolo F, Menegatti E, Federici L, Moretti C, Brancati F.
    Gynecol Endocrinol; 2017 Dec 21; 33(12):918-922. PubMed ID: 28609197
    [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 21; 56(4):504-7. PubMed ID: 17379008
    [Abstract] [Full Text] [Related]

  • 19. Steroid 11beta- hydroxylase deficiency congenital adrenal hyperplasia.
    Nimkarn S, New MI.
    Trends Endocrinol Metab; 2008 Apr 21; 19(3):96-9. PubMed ID: 18294861
    [Abstract] [Full Text] [Related]

  • 20. Point mutation of Arg440 to His in cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency.
    Fardella CE, Hum DW, Homoki J, Miller WL.
    J Clin Endocrinol Metab; 1994 Jul 21; 79(1):160-4. PubMed ID: 8027220
    [Abstract] [Full Text] [Related]

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