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PUBMED FOR HANDHELDS

Journal Abstract Search


221 related items for PubMed ID: 33960260

  • 1. 18-Year-old patient with Klinefelter syndrome (47, XXY) and complete androgen insensitivity syndrome (CAIS) - case report.
    Skalska K, Ziółkowski M, Skoczylas A, Teleon M, Grymowicz M, Pollak A, Smolarczyk R, Płoski R, Męczekalski B.
    Gynecol Endocrinol; 2021 Jun; 37(6):572-575. PubMed ID: 33960260
    [Abstract] [Full Text] [Related]

  • 2. Primary amenorrhea in a young Polish woman with complete androgen insensitivity syndrome and Sertoli-Leydig cell tumor: identification of a new androgen receptor gene mutation and evidence of aromatase hyperactivity and apoptosis dysregulation within the tumor.
    Jarzabek K, Philibert P, Koda M, Sulkowski S, Kotula-Balak M, Bilinska B, Kottler ML, Wolczynski S, Sultan C.
    Gynecol Endocrinol; 2007 Sep; 23(9):499-504. PubMed ID: 17852420
    [Abstract] [Full Text] [Related]

  • 3. Heterozygous Nonsense Mutation in the Androgen Receptor Gene Associated with Partial Androgen Insensitivity Syndrome in an Individual with 47,XXY Karyotype.
    Batista RL, Rodrigues AS, Nishi MY, Feitosa ACR, Gomes NLRA, Junior JAF, Domenice S, Costa EMF, de Mendonça BB.
    Sex Dev; 2017 Sep; 11(2):78-81. PubMed ID: 28456808
    [Abstract] [Full Text] [Related]

  • 4. An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome.
    Ha TMT, Le PTQ, Le TNU, Hoang TTY.
    Nagoya J Med Sci; 2023 May; 85(2):362-368. PubMed ID: 37346838
    [Abstract] [Full Text] [Related]

  • 5. Clinical characteristics and molecular genetics of complete androgen insensitivity syndrome patients: a series study of 30 cases from a Chinese tertiary medical center.
    Zhang D, Yao F, Tian T, Deng S, Luo M, Tian Q.
    Fertil Steril; 2021 May; 115(5):1270-1279. PubMed ID: 33602557
    [Abstract] [Full Text] [Related]

  • 6. A case of complete androgen insensitivity syndrome with a novel androgen receptor mutation.
    Chin VL, Sheffer-Babila S, Lee TA, Tanaka K, Zhou P.
    J Pediatr Endocrinol Metab; 2012 May; 25(11-12):1145-51. PubMed ID: 23329762
    [Abstract] [Full Text] [Related]

  • 7. Complete androgen insensitivity syndrome: a case report and literature review.
    Guo M, Huang JC, Li CF, Liu YY.
    J Int Med Res; 2023 Feb; 51(2):3000605231154413. PubMed ID: 36851849
    [Abstract] [Full Text] [Related]

  • 8. Frequency of gonadal tumours in complete androgen insensitivity syndrome (CAIS): A retrospective case-series analysis.
    Chaudhry S, Tadokoro-Cuccaro R, Hannema SE, Acerini CL, Hughes IA.
    J Pediatr Urol; 2017 Oct; 13(5):498.e1-498.e6. PubMed ID: 28351649
    [Abstract] [Full Text] [Related]

  • 9. Clinical, hormonal and genetic characteristics of androgen insensitivity syndrome in 39 Chinese patients.
    Liu Q, Yin X, Li P.
    Reprod Biol Endocrinol; 2020 Apr 28; 18(1):34. PubMed ID: 32345305
    [Abstract] [Full Text] [Related]

  • 10. Complete androgen insensitivity syndrome in a young woman with metabolic disorder and diabetes: A case report.
    Yang P, Liu X, Gao J, Qu S, Zhang M.
    Medicine (Baltimore); 2018 Aug 28; 97(33):e11353. PubMed ID: 30113450
    [Abstract] [Full Text] [Related]

  • 11. Complete Androgen Insensitivity Syndrome: From the Relevance of an Accurate Genetic Diagnosis to the Challenge of Clinical Management. A Case Report.
    Barbagallo F, Cannarella R, Bertelli M, Crafa A, La Vignera S, Condorelli RA, Calogero AE.
    Medicina (Kaunas); 2021 Oct 21; 57(11):. PubMed ID: 34833359
    [Abstract] [Full Text] [Related]

  • 12. R831X mutation of the androgen receptor gene in an adolescent with complete androgen insensitivity syndrome and bilateral testicular hamartomata.
    Goulis DG, Iliadou PK, Papanicolaou A, Georgiou I, Chatzikyriakidou A, Gerou S, Bondis IN, Papadimas I.
    Hormones (Athens); 2006 Oct 21; 5(3):200-4. PubMed ID: 16950754
    [Abstract] [Full Text] [Related]

  • 13. [Genetic analysis and prenatal diagnosis of a Chinese pedigree affected with Complete androgen insensitivity syndrome due to a novel variant of AR gene].
    Meng F, Li X, Shi Y, Ju D, Wang X, Wang C, Li X, Yu W, Wang Y, Zhou X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Oct 10; 41(10):1206-1212. PubMed ID: 39344615
    [Abstract] [Full Text] [Related]

  • 14. Complete androgen insensitivity syndrome in juveniles and adults with female phenotypes.
    Wang Z, Sa YL, Ye XX, Zhang J, Xu YM.
    J Obstet Gynaecol Res; 2014 Sep 10; 40(9):2044-50. PubMed ID: 25170741
    [Abstract] [Full Text] [Related]

  • 15. Complete androgen insensitivity syndrome in a 13-year-old Lebanese child, reared as female, with bilateral inguinal hernia: a case report.
    Farah S, El Masri D, Hirbli K.
    J Med Case Rep; 2021 Apr 17; 15(1):202. PubMed ID: 33863387
    [Abstract] [Full Text] [Related]

  • 16. Androgen insensitivity syndrome.
    Hughes IA, Werner R, Bunch T, Hiort O.
    Semin Reprod Med; 2012 Oct 17; 30(5):432-42. PubMed ID: 23044881
    [Abstract] [Full Text] [Related]

  • 17. Features of the fetal gonad in androgen synthesis in the postpubertal testis are preserved in complete androgen insensitivity syndrome due to a novel genetic splice site donor variant in androgen receptor gene intron 1.
    Jarzabek K, Koda M, Chrusciel M, Kanczuga-Koda L, Sobczynska-Tomaszewska A, Rahman NA, Wolczynski S.
    J Steroid Biochem Mol Biol; 2019 Oct 17; 193():105420. PubMed ID: 31283987
    [Abstract] [Full Text] [Related]

  • 18. 47,XXY female with testicular feminization and positive SRY: a case report.
    Saavedra-Castillo E, Cortés-Gutiérrez EI, Dávila-Rodríguez MI, Reyes-Martínez ME, Oliveros-Rodríguez A.
    J Reprod Med; 2005 Feb 17; 50(2):138-40. PubMed ID: 15755052
    [Abstract] [Full Text] [Related]

  • 19. Novel androgen receptor gene mutation in patient with complete androgen insensitivity syndrome.
    Ning Y, Zhang F, Zhu Y, Chen H, Lu J, Li Z.
    Urology; 2012 Jul 17; 80(1):216-8. PubMed ID: 22608796
    [Abstract] [Full Text] [Related]

  • 20. [A case of complete androgen insensitivity syndrome with special family history and its genetic analysis].
    Wang YH, Chen XL, Qin C, Su SF.
    Zhonghua Nan Ke Xue; 2022 Jul 17; 28(7):618-621. PubMed ID: 37556220
    [Abstract] [Full Text] [Related]


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