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Journal Abstract Search

130 related items for PubMed ID: 20960109

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

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

  • 3. 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 Feb; 17(1):43-50. PubMed ID: 36652930
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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; 34(6):540-544. PubMed ID: 29345162
    [Abstract] [Full Text] [Related]

  • 6. Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency.
    Kurnaz E, Kartal Baykan E, Türkyılmaz A, Yaralı O, Yavaş Abalı Z, Turan S, Bereket A, Çayır A, Guran T.
    Horm Res Paediatr; 2020 Jun; 93(9-10):558-566. PubMed ID: 33780934
    [Abstract] [Full Text] [Related]

  • 7. 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; 23(5):576-582. PubMed ID: 28225307
    [Abstract] [Full Text] [Related]

  • 8. 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; 36(1):24-29. PubMed ID: 31464148
    [Abstract] [Full Text] [Related]

  • 9. 17α-hydroxlyase/17, 20-lyase deficiency in three siblings with primary amenorrhea and absence of secondary sexual development.
    Oh YK, Ryoo U, Kim D, Cho SY, Jin DK, Yoon BK, Lee DY, Choi D.
    J Pediatr Adolesc Gynecol; 2012 Oct; 25(5):e103-5. PubMed ID: 22841373
    [Abstract] [Full Text] [Related]

  • 10. 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; 28(9):733-5. PubMed ID: 22309630
    [Abstract] [Full Text] [Related]

  • 11. 17-alpha-hydroxylase deficiency: a case report with clinical and molecular analysis.
    Li H, Qiao J, Guo H.
    Gynecol Endocrinol; 2010 Jul; 26(7):521-3. PubMed ID: 20170344
    [Abstract] [Full Text] [Related]

  • 12. 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; 15(1):339-344. PubMed ID: 27959413
    [Abstract] [Full Text] [Related]

  • 13. Genetic diagnosis and clinical analysis of 17α-hydroxylase/17, 20-lyase deficiency combined with type 2 diabetes mellitus: A case report.
    Zhang Y, Yuan Y.
    Medicine (Baltimore); 2023 Dec 29; 102(52):e36727. PubMed ID: 38206738
    [Abstract] [Full Text] [Related]

  • 14. 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 29; 32(4):322-4. PubMed ID: 19636199
    [Abstract] [Full Text] [Related]

  • 15. A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations.
    Kardelen AD, Toksoy G, Baş F, Yavaş Abalı Z, Gençay G, Poyrazoğlu Ş, Bundak R, Altunoğlu U, Avcı Ş, Najaflı A, Uyguner O, Karaman B, Başaran S, Darendeliler F.
    J Clin Res Pediatr Endocrinol; 2018 Jul 31; 10(3):206-215. PubMed ID: 29595516
    [Abstract] [Full Text] [Related]

  • 16. Steroid 17-hydroxylase and 17,20-lyase deficiencies, genetic and pharmacologic.
    Auchus RJ.
    J Steroid Biochem Mol Biol; 2017 Jan 31; 165(Pt A):71-78. PubMed ID: 26862015
    [Abstract] [Full Text] [Related]

  • 17. Phenotypic Heterogeneity and Fertility Potential of Patients With 17-Hydroxylase/17,20-lyase Deficiency.
    Xu Y, Jiang S, Yan Z, Niu Y, Du W, Liu B, Han B, Liu X, Zhao S, Song H, Kuang Y, Qiao J.
    J Clin Endocrinol Metab; 2022 May 17; 107(6):e2610-e2618. PubMed ID: 35043964
    [Abstract] [Full Text] [Related]

  • 18. Clinical Features of Unrecognized Congenital Adrenal Hyperplasia Due to 17α-hydroxylase Deficiency Since Adolescence: A Case Report.
    Rashmi KG, Ravichandran L, Roy A, Naik D, Kamalanathan S, Sahoo J, Chapla A, Thomas N.
    J ASEAN Fed Endocr Soc; 2023 May 17; 38(2):131-134. PubMed ID: 38045661
    [Abstract] [Full Text] [Related]

  • 19. Two rare forms of congenital adrenal hyperplasia, 11β hydroxylase deficiency and 17-hydroxylase/17,20-lyase deficiency, presenting with novel mutations.
    Bulsari K, Maple-Brown L, Falhammar H.
    Hormones (Athens); 2018 Mar 17; 17(1):127-132. PubMed ID: 29858860
    [Abstract] [Full Text] [Related]

  • 20. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 Mar 17; 52(11-12):447-54. PubMed ID: 10748766
    [Abstract] [Full Text] [Related]

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