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Journal Abstract Search

723 related items for PubMed ID: 15522944

  • 1. Androgen insensitivity syndrome: somatic mosaicism of the androgen receptor in seven families and consequences for sex assignment and genetic counseling.
    Köhler B, Lumbroso S, Leger J, Audran F, Grau ES, Kurtz F, Pinto G, Salerno M, Semitcheva T, Czernichow P, Sultan C.
    J Clin Endocrinol Metab; 2005 Jan; 90(1):106-11. PubMed ID: 15522944
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  • 4. Partial androgen insensitivity syndrome due to somatic mosaicism of the androgen receptor.
    Batista RL, Rodrigues AS, Machado AZ, Nishi MY, Cunha FS, Silva RB, Costa EMF, Mendonca BB, Domenice S.
    J Pediatr Endocrinol Metab; 2018 Jan 26; 31(2):223-228. PubMed ID: 29267169
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  • 5. Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome.
    Ahmed SF, Cheng A, Dovey L, Hawkins JR, Martin H, Rowland J, Shimura N, Tait AD, Hughes IA.
    J Clin Endocrinol Metab; 2000 Feb 26; 85(2):658-65. PubMed ID: 10690872
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  • 6. 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
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  • 9. Clinical and molecular spectrum of somatic mosaicism in androgen insensitivity syndrome.
    Holterhus PM, Wiebel J, Sinnecker GH, Brüggenwirth HT, Sippell WG, Brinkmann AO, Kruse K, Hiort O.
    Pediatr Res; 1999 Dec 28; 46(6):684-90. PubMed ID: 10590024
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  • 10. AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity.
    Akcay T, Fernandez-Cancio M, Turan S, Güran T, Audi L, Bereket A.
    Andrology; 2014 Jul 28; 2(4):572-8. PubMed ID: 24737579
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  • 11. Expression of two functionally different androgen receptors in a patient with androgen insensitivity.
    Holterhus PM, Sinnecker GH, Wollmann HA, Struve D, Homburg N, Kruse K, Hiort O.
    Eur J Pediatr; 1999 Sep 28; 158(9):702-6. PubMed ID: 10485299
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  • 12. Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center Cohort.
    Touzon MS, Garrido NP, Marino R, Ramirez P, Costanzo M, Guercio G, Berensztein E, Rivarola MA, Belgorosky A.
    J Clin Res Pediatr Endocrinol; 2019 Feb 20; 11(1):24-33. PubMed ID: 30251955
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  • 13. Long-term followup and comparison between genotype and phenotype in 29 cases of complete androgen insensitivity syndrome.
    Cheikhelard A, Morel Y, Thibaud E, Lortat-Jacob S, Jaubert F, Polak M, Nihoul-Fekete C.
    J Urol; 2008 Oct 20; 180(4):1496-501. PubMed ID: 18710728
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  • 15. Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome.
    Chávez B, Méndez JP, Ulloa-Aguirre A, Larrea F, Vilchis F.
    J Hum Genet; 2001 Oct 20; 46(10):560-5. PubMed ID: 11587068
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  • 19. Mutations in the amino-terminal domain of the human androgen receptor may be associated with partial androgen insensitivity and impaired transactivation in vitro.
    Holterhus PM, Werner R, Struve D, Hauffa BP, Schroeder C, Hiort O.
    Exp Clin Endocrinol Diabetes; 2005 Sep 20; 113(8):457-63. PubMed ID: 16151980
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  • 20. Clinical and biochemical investigations and molecular analysis of subjects with mutations in the androgen receptor gene.
    Weidemann W, Linck B, Haupt H, Mentrup B, Romalo G, Stockklauser K, Brinkmann AO, Schweikert HU, Spindler KD.
    Clin Endocrinol (Oxf); 1996 Dec 20; 45(6):733-9. PubMed ID: 9039340
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