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Journal Abstract Search

157 related items for PubMed ID: 28739554

  • 41. Complexities of gender assignment in 17β-hydroxysteroid dehydrogenase type 3 deficiency: is there a role for early orchiectomy?
    Chuang J, Vallerie A, Breech L, Saal HM, Alam S, Crawford P, Rutter MM.
    Int J Pediatr Endocrinol; 2013 Sep 12; 2013(1):15. PubMed ID: 24025597
    [Abstract] [Full Text] [Related]

  • 42. 17β-Hydroxysteroid dehydrogenase 3 deficiency: Three case reports and a systematic review.
    Yang Z, Ye L, Wang W, Zhao Y, Wang W, Jia H, Dong Z, Chen Y, Wang W, Ning G, Sun S.
    J Steroid Biochem Mol Biol; 2017 Nov 12; 174():141-145. PubMed ID: 28847746
    [Abstract] [Full Text] [Related]

  • 43. Four novel mutations identification in 17 beta-hydroxysteroid dehydrogenase-3 deficiency and our clinical experience: possible benefits of early treatment.
    Wang Y, Xu Y, Zhang H, Yin D, Pan Y, He X, Li S, Cheng Z, Zhu G, Zhao T, Huang H, Zhu M.
    Front Endocrinol (Lausanne); 2023 Nov 12; 14():1267967. PubMed ID: 38425490
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  • 44. 17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence.
    Bertelloni S, Balsamo A, Giordani L, Fischetto R, Russo G, Delvecchio M, Gennari M, Nicoletti A, Maggio MC, Concolino D, Cavallo L, Cicognani A, Chiumello G, Hiort O, Baroncelli GI, Faienza MF.
    J Endocrinol Invest; 2009 Sep 12; 32(8):666-70. PubMed ID: 19498320
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  • 45. Serum steroid metabolite profiling by LC-MS/MS in two phenotypic male patients with HSD17B3 deficiency: Implications for hormonal diagnosis.
    Fujisawa Y, Masunaga Y, Tanikawa W, Nakashima S, Ueda D, Sano S, Fukami M, Saitsu H, Yazawa T, Ogata T.
    J Steroid Biochem Mol Biol; 2023 Nov 12; 234():106403. PubMed ID: 37741351
    [Abstract] [Full Text] [Related]

  • 46. 17β-hydroxysteroid dehydrogenase type 3 deficiency: female sex assignment and follow-up.
    Faienza MF, Baldinotti F, Marrocco G, TyuTyusheva N, Peroni D, Baroncelli GI, Bertelloni S.
    J Endocrinol Invest; 2020 Dec 12; 43(12):1711-1716. PubMed ID: 32297288
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  • 47. 17beta-hydroxysteroid dehydrogenase-3 deficiency: a rare endocrine cause of male-to-female sex reversal.
    Bertelloni S, Maggio MC, Federico G, Baroncelli G, Hiort O.
    Gynecol Endocrinol; 2006 Sep 12; 22(9):488-94. PubMed ID: 17071532
    [Abstract] [Full Text] [Related]

  • 48. Novel mutations of HSD17B3 in three Chinese patients with 46,XY Disorders of Sex Development.
    Yu B, Liu Z, Mao J, Wang X, Zheng J, Xiong S, Cui M, Ma W, Huang Q, Xu H, Huang B, Nie M, Wu X.
    Steroids; 2017 Oct 12; 126():1-6. PubMed ID: 28774765
    [Abstract] [Full Text] [Related]

  • 49. HSD17B1 Compensates for HSD17B3 Deficiency in Fetal Mouse Testis but Not in Adults.
    Junnila A, Zhang FP, Martínez Nieto G, Hakkarainen J, Mäkelä JA, Ohlsson C, Sipilä P, Poutanen M.
    Endocrinology; 2024 Apr 29; 165(6):. PubMed ID: 38785348
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  • 50. Initial assessment of a child with suspected disorder of sex development.
    Ahmad A, Ayub F, Saleem I, Ahmad N.
    J Pak Med Assoc; 2019 May 29; 69(5):711-717. PubMed ID: 31105293
    [Abstract] [Full Text] [Related]

  • 51. Steroid 17β-hydroxysteroid dehydrogenase deficiency in man: an inherited form of male pseudohermaphroditism.
    Rösler A.
    J Steroid Biochem Mol Biol; 1992 Dec 29; 43(8):989-1002. PubMed ID: 22217844
    [Abstract] [Full Text] [Related]

  • 52. Germ cell neoplasia in situ complicating 17β-hydroxysteroid dehydrogenase type 3 deficiency.
    Folsom LJ, Hjaige M, Liu J, Eugster EA, Auchus RJ.
    Mol Cell Endocrinol; 2019 Jun 01; 489():3-8. PubMed ID: 30508571
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  • 53. Deficiency of 17-ketoreductase presenting before puberty.
    Gregory JW, Aynsley-Green A, Evans BA, Hughes IA, Werder EA, Zachmann M.
    Horm Res; 1993 Jun 01; 40(4):145-8. PubMed ID: 8300063
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  • 54. Novel mutations of the SRD5A2 and AR genes in Thai patients with 46, XY disorders of sex development.
    Ittiwut C, Pratuangdejkul J, Supornsilchai V, Muensri S, Hiranras Y, Sahakitrungruang T, Watcharasindhu S, Suphapeetiporn K, Shotelersuk V.
    J Pediatr Endocrinol Metab; 2017 Jan 01; 30(1):19-26. PubMed ID: 27849622
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  • 55. Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase 3 deficiency. Diagnosis, psychological evaluation, and management.
    Mendonca BB, Inacio M, Arnhold IJ, Costa EM, Bloise W, Martin RM, Denes FT, Silva FA, Andersson S, Lindqvist A, Wilson JD.
    Medicine (Baltimore); 2000 Sep 01; 79(5):299-309. PubMed ID: 11039078
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  • 56. Whole exome sequencing and functional characterization increase diagnostic yield in siblings with a 46, XY difference of sexual development (DSD).
    Luna SE, Wegner DJ, Gale S, Yang P, Hollander A, St Dennis-Feezle L, Nabhan ZM, Ory DS, Cole FS, Wambach JA.
    J Steroid Biochem Mol Biol; 2021 Sep 01; 212():105908. PubMed ID: 33984517
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  • 57. 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
    Rosler A.
    Pediatr Endocrinol Rev; 2006 Aug 01; 3 Suppl 3():455-61. PubMed ID: 17551466
    [Abstract] [Full Text] [Related]

  • 58. Familial male pseudohermaphroditism with gynaecomastia due to 17 beta-hydroxysteroid dehydrogenase deficiency. A report of 3 cases.
    Balducci R, Toscano V, Wright F, Bozzolan F, Di Piero G, Maroder M, Panei P, Sciarra F, Boscherini B.
    Clin Endocrinol (Oxf); 1985 Oct 01; 23(4):439-44. PubMed ID: 2998649
    [Abstract] [Full Text] [Related]

  • 59. A novel missense (R80W) mutation in 17-beta-hydroxysteroid dehydrogenase type 3 gene associated with male pseudohermaphroditism.
    Bilbao JR, Loridan L, Audí L, Gonzalo E, Castaño L.
    Eur J Endocrinol; 1998 Sep 01; 139(3):330-3. PubMed ID: 9758445
    [Abstract] [Full Text] [Related]

  • 60. 46,XY disorder of sex development due to 17-beta hydroxysteroid dehydrogenase type 3 deficiency: a plea for timely genetic testing.
    Grimbly C, Caluseriu O, Metcalfe P, Jetha MM, Rosolowsky ET.
    Int J Pediatr Endocrinol; 2016 Sep 01; 2016():12. PubMed ID: 27307783
    [Abstract] [Full Text] [Related]

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