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Journal Abstract Search

147 related items for PubMed ID: 21823532

  • 1. Rare hypertension as a result of 17alpha-hydroxylase deficiency.
    Wang W, Fu JF, Gong FQ, Zhu WH, Shen Z.
    J Pediatr Endocrinol Metab; 2011; 24(5-6):333-7. PubMed ID: 21823532
    [Abstract] [Full Text] [Related]

  • 2. Study on the genetic mutations of 17 alpha-hydroxylase/17,20-lyase deficiency in Chinese patients.
    Tao H, Lu ZL, Zhang B, Mi SH, Wang NY, Wang XZ, Wu J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Apr; 23(2):125-8. PubMed ID: 16604478
    [Abstract] [Full Text] [Related]

  • 3. Phenotype-genotype correlation in eight Chinese 17alpha-hydroxylase/17,20 lyase-deficiency patients with five novel mutations of CYP17A1 gene.
    Yang J, Cui B, Sun S, Shi T, Zheng S, Bi Y, Liu J, Zhao Y, Chen J, Ning G, Li X.
    J Clin Endocrinol Metab; 2006 Sep; 91(9):3619-25. PubMed ID: 16772352
    [Abstract] [Full Text] [Related]

  • 4. [New compound heterozygous mutation causes partial combined 17 alpha-hydroxylase/17,20-lyase deficiency].
    Tao H, Zhang B, Lu ZL, Pei Y, Mi SH.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb; 24(1):19-22. PubMed ID: 17285537
    [Abstract] [Full Text] [Related]

  • 5. New, recurrent, and prevalent mutations: Clinical and molecular characterization of 26 Chinese patients with 17alpha-hydroxylase/17,20-lyase deficiency.
    Zhang M, Sun S, Liu Y, Zhang H, Jiao Y, Wang W, Li X.
    J Steroid Biochem Mol Biol; 2015 Jun; 150():11-6. PubMed ID: 25697092
    [Abstract] [Full Text] [Related]

  • 6. 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; 24(133):175-182. PubMed ID: 29278670
    [Abstract] [Full Text] [Related]

  • 7. A new compound heterozygous mutation in the CYP17A1 gene in a female with 17α-hydroxylase/17,20-lyase deficiency.
    Lee ES, Kim M, Moon S, Jekarl DW, Lee S, Kim Y, Choi GY.
    Gynecol Endocrinol; 2013 Jul; 29(7):720-3. PubMed ID: 23772786
    [Abstract] [Full Text] [Related]

  • 8. Phenotypic variation in a Chinese family with 46,XY and 46,XX 17α-hydroxylase deficiency.
    Bee YM, Manju C, Papari-Zareei M, Auchus RJ.
    Gynecol Endocrinol; 2012 Apr; 28(4):322-5. PubMed ID: 22087567
    [Abstract] [Full Text] [Related]

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  • 10. Genotyping of five chinese patients with 17alpha-hydroxylase deficiency diagnosed through high-performance liquid chromatography serum adrenal profile: identification of two novel CYP17 mutations.
    Wei JQ, Wei JL, Li WC, Bi YS, Wei FC.
    J Clin Endocrinol Metab; 2006 Sep; 91(9):3647-53. PubMed ID: 16822828
    [Abstract] [Full Text] [Related]

  • 11. CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiency.
    Yao F, Huang S, Kang X, Zhang W, Wang P, Tian Q.
    Gynecol Endocrinol; 2013 Jan; 29(1):10-5. PubMed ID: 22954317
    [Abstract] [Full Text] [Related]

  • 12. Novel CYP17A1 mutation in a Japanese patient with combined 17alpha-hydroxylase/17,20-lyase deficiency.
    Katsumata N, Ogawa E, Fujiwara I, Fujikura K.
    Metabolism; 2010 Feb; 59(2):275-8. PubMed ID: 19793597
    [Abstract] [Full Text] [Related]

  • 13. [Analysis of CYP17A1 gene mutation in a child patient with 17 alpha-hydroxylase/17, 20-lyase deficiency].
    Yang K, Zhang B, Cui SX, Guo QN, Hou QF, Li QC, Liao SX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):439-42. PubMed ID: 23926012
    [Abstract] [Full Text] [Related]

  • 14. [A compound heterozygous mutation in CYP17A1 gene in a female subject with partial 17α-hydroxylase/17, 20 lyase deficiency].
    Jiang Y, Zhang D, Nie M, Xiao XH, Yu Q, Lu ZL.
    Zhonghua Yi Xue Za Zhi; 2011 Sep 13; 91(34):2416-9. PubMed ID: 22321788
    [Abstract] [Full Text] [Related]

  • 15. A novel compound heterozygous mutation of K494_V495 deletion plus R496L and D487_F489 deletion in extreme C-terminus of cytochrome P450c17 causes 17alpha-hydroxylase deficiency.
    Lee LS, Shu WJ, Wu CM, Hsieh CH, Chen SM, Hu CJ, Chen WY, Chung BC.
    Mol Cell Endocrinol; 2006 Apr 25; 249(1-2):16-20. PubMed ID: 16483711
    [Abstract] [Full Text] [Related]

  • 16. A review of the literature on common CYP17A1 mutations in adults with 17-hydroxylase/17,20-lyase deficiency, a case series of such mutations among Koreans and functional characteristics of a novel mutation.
    Kim YM, Kang M, Choi JH, Lee BH, Kim GH, Ohn JH, Kim SY, Park MS, Yoo HW.
    Metabolism; 2014 Jan 25; 63(1):42-9. PubMed ID: 24140098
    [Abstract] [Full Text] [Related]

  • 17. [Clinical and molecular genetic analysis for 7 patients from 5 pedigrees with 17a-hydroxylase/17, 20 lyase deficiency].
    Liu BL, Qiao J, Chen X, Liang J, Zuo CL, Gu YY, Han B, Gong J, Ru Y, Lu YL, Wu WL, Chen MD, Song HD.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun 25; 26(3):282-7. PubMed ID: 19504440
    [Abstract] [Full Text] [Related]

  • 18. CYP17A1 gene mutations and hypertension variations found in 46, XY females with combined 17α-hydroxylase/17, 20-lyase deficiency.
    Wang YP, Zhao YJ, Zhou GY, He B.
    Gynecol Endocrinol; 2014 Jun 25; 30(6):456-60. PubMed ID: 24597476
    [Abstract] [Full Text] [Related]

  • 19. Homozygous CYP17A1 mutation (H373L) identified in a 46,XX female with combined 17α-hydroxylase/17,20-lyase deficiency.
    Lee MH, Won Park S, Yoon TK, Shim SH.
    Gynecol Endocrinol; 2012 Jul 25; 28(7):573-6. PubMed ID: 22452398
    [Abstract] [Full Text] [Related]

  • 20. Identification of steroid biosynthetic defects in genotype-proven heterozygous individuals for 17alpha-hydroxylase/17,20-lyase deficiency.
    Qiao J, Chen X, Zuo CL, Gu YY, Liu BL, Liang J, Lu YL, Tang JF, Wu YX, Chen MD, Chen JL, Wu WL, Song HD.
    Clin Endocrinol (Oxf); 2010 Mar 25; 72(3):312-9. PubMed ID: 19508587
    [Abstract] [Full Text] [Related]

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