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Journal Abstract Search

82 related items for PubMed ID: 18241541

  • 1. [Incomplete P450 17 alpha enzyme deficiency: report of six cases].
    Tian QJ, Zhang YW, Lu ZL, Sha GH, Gao H.
    Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):670-4. PubMed ID: 18241541
    [Abstract] [Full Text] [Related]

  • 2. Partial 17alpha-hydroxylase/17,20-lyase deficiency-clinical report of five Chinese 46,XX cases.
    Tian Q, Zhang Y, Lu Z.
    Gynecol Endocrinol; 2008 Jul; 24(7):362-7. PubMed ID: 18645707
    [Abstract] [Full Text] [Related]

  • 3. [Clinical study on 48 cases with complete 17α-hydroxylase deficiency].
    Wang HB, Tian QJ, Sun AJ, Yao FX, Kang XD, Zhang Y, Chen R.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Jul; 47(7):518-21. PubMed ID: 23141163
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  • 4. Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign.
    Çamtosun E, Şıklar Z, Ceylaner S, Kocaay P, Berberoğlu M.
    J Clin Res Pediatr Endocrinol; 2017 Jun 01; 9(2):163-167. PubMed ID: 28008861
    [Abstract] [Full Text] [Related]

  • 5. 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 01; 23(2):94-8. PubMed ID: 17454159
    [Abstract] [Full Text] [Related]

  • 6. A novel homozygous CYP17A1 mutation causes partial 17 α-hydroxylase/17,20-lyase deficiency in 46,XX: a case report and literature review.
    Chen H, Chen Y, Mao H, Huang H, Lou X.
    Blood Press; 2023 Dec 01; 32(1):2195008. PubMed ID: 37088984
    [Abstract] [Full Text] [Related]

  • 7. [Clinical characteristics of 17alpha-hydroxylase/17,20-lyase deficiency and long term follow up results].
    Tao H, Lu ZL, Zhang B, Wang Y, Sun ML.
    Zhonghua Nei Ke Za Zhi; 2005 Jun 01; 44(6):442-5. PubMed ID: 16008859
    [Abstract] [Full Text] [Related]

  • 8. 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
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  • 10. 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 01; 101(2):317-22. PubMed ID: 24485502
    [Abstract] [Full Text] [Related]

  • 11. Deficiency of 17,20-lyase causing giant ovarian cysts in a girl and a female phenotype in her 46,XY sister: case report.
    ten Kate-Booij MJ, Cobbaert C, Koper JW, de Jong FH.
    Hum Reprod; 2004 Feb 01; 19(2):456-9. PubMed ID: 14747197
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 44(5):477-8. PubMed ID: 15387879
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  • 14. Combined 17α-hydroxylase/17,20-lyase deficiency with short stature: case study.
    Ma L, Peng F, Yu L, Chen J, Ji W, Zhang C, Zhang X.
    Gynecol Endocrinol; 2016 Oct 01; 32(4):264-6. PubMed ID: 26607998
    [Abstract] [Full Text] [Related]

  • 15. Clinical characteristics and molecular etiology of partial 17α-hydroxylase deficiency diagnosed in 46,XX patients.
    Zhang D, Yao F, Luo M, Wang Y, Tian T, Deng S, Tian Q.
    Front Endocrinol (Lausanne); 2022 Oct 01; 13():978026. PubMed ID: 36589849
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 15(1):339-344. PubMed ID: 27959413
    [Abstract] [Full Text] [Related]

  • 17. [A novel homozygous mutation p.E25X in the HSD3B2 gene causing salt wasting 3β-hydroxysteroid dehydrogenases deficiency in a Chinese pubertal girl: a delayed diagnosis until recurrent ovary cysts].
    Huang Y, Zheng J, Xie T, Xiao Q, Lu S, Li X, Cheng J, Chen L, Liu L.
    Zhonghua Er Ke Za Zhi; 2014 Dec 01; 52(12):948-51. PubMed ID: 25619355
    [Abstract] [Full Text] [Related]

  • 18. Seventeen alpha-hydroxylase deficiency.
    Wong SL, Shu SG, Tsai CR.
    J Formos Med Assoc; 2006 Feb 01; 105(2):177-81. PubMed ID: 16477341
    [Abstract] [Full Text] [Related]

  • 19. [Identification of congenital adrenal hyperplasia by measurement of blood-spot 17-hydroxyprogesterone].
    Sólyom J, Eckhardt G, Török D.
    Orv Hetil; 2004 Oct 03; 145(40):2051-6. PubMed ID: 15559532
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