BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

381 related articles for article (PubMed ID: 11530701)

  • 1. [Differential diagnosis and treatment of girls with 46XY-karyotype and androgen insensitivity syndrome].
    Drop SL; Boehmer AL; Slijper FM; Nijman JM; Hazebroek FW; Niermeijer MF
    Ned Tijdschr Geneeskd; 2001 Apr; 145(14):665-9. PubMed ID: 11530701
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Androgen insensitivity syndrome].
    Giwercman YL; Svensson J
    Tidsskr Nor Laegeforen; 2008 Feb; 128(5):581-5. PubMed ID: 18311203
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Incomplete androgen insensitivity].
    Luczay A; Sólyom J; Hiort O; Szabó E; Dobos M; Jenovári Z; Fekete G
    Orv Hetil; 2006 Sep; 147(37):1805-7. PubMed ID: 17131800
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Androgen resistance.
    Hughes IA; Deeb A
    Best Pract Res Clin Endocrinol Metab; 2006 Dec; 20(4):577-98. PubMed ID: 17161333
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome].
    Soriano Guillén L; Muñoz Calvo MT; Martinez Pérez J; Pozo Román J; Martín Sobrino MA; González Medeiro I; Argente Oliver J
    An Esp Pediatr; 2002 Apr; 56(4):347-52. PubMed ID: 11927080
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 180(4):1496-501. PubMed ID: 18710728
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial androgen insensitivity syndrome with R840H mutation in androgen receptor: report of one case.
    Yen JL; Chang KH; Sheu JC; Lee YJ; Tsai LP
    Acta Paediatr Taiwan; 2005; 46(2):101-5. PubMed ID: 16302589
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a critical novel mutation in the exon 1 of androgen receptor gene in 2 brothers with complete androgen insensitivity syndrome.
    Radpour R; Falah M; Aslani A; Zhong XY; Saleki A
    J Androl; 2009; 30(3):230-2. PubMed ID: 19023143
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Disorders of androgen action.
    Sultan C; Lumbroso S; Paris F; Jeandel C; Terouanne B; Belon C; Audran F; Poujol N; Georget V; Gobinet J; Jalaguier S; Auzou G; Nicolas JC
    Semin Reprod Med; 2002 Aug; 20(3):217-28. PubMed ID: 12428202
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of a novel receptor mutation A-->T at exon 4 in complete androgen insensitivity syndrome and a carrier sibling via bidirectional polymorphism sequence analysis.
    Sills ES; Sholes TE; Perloe M; Kaplan CR; Davis JG; Tucker MJ
    Int J Mol Med; 2002 Jan; 9(1):45-8. PubMed ID: 11744994
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome.
    Raicu F; Giuliani R; Gatta V; Palka C; Franchi PG; Lelli-Chiesa P; Tumini S; Stuppia L
    Asian J Androl; 2008 Jul; 10(4):687-91. PubMed ID: 18097502
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Androgen insensitivity syndrome.
    Mendoza N; Motos MA
    Gynecol Endocrinol; 2013 Jan; 29(1):1-5. PubMed ID: 22812659
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ala 586 Asp mutation in androgen receptor disrupts transactivation function without affecting androgen binding.
    Rajender S; Gupta NJ; Chakrabarty B; Singh L; Thangaraj K
    Fertil Steril; 2009 Mar; 91(3):933.e23-8. PubMed ID: 19062009
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Severe 46,XY virilization deficit due to 17beta-hydroxysteroid dehydrogenase deficiency].
    Twesten W; Johannisson R; Holterhus PM; Hiort O
    Klin Padiatr; 2002; 214(5):314-5. PubMed ID: 12235550
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular studies of a patient with complete androgen insensitivity and a 47,XXY karyotype.
    Girardin CM; Deal C; Lemyre E; Paquette J; Lumbroso R; Beitel LK; Trifiro MA; Van Vliet G
    J Pediatr; 2009 Sep; 155(3):439-43. PubMed ID: 19732585
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Complete androgen insensitivity without Wolffian duct development: the AR-A form of the androgen receptor is not sufficient for male genital development.
    Barbaro M; Oscarson M; Almskog I; Hamberg H; Wedell A
    Clin Endocrinol (Oxf); 2007 Jun; 66(6):822-6. PubMed ID: 17408421
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Androgen insensitivity syndrome. Clinical features and molecular genetics].
    Sólyom J; Scheiber D; Fekete G
    Orv Hetil; 2001 Aug; 142(31):1659-65. PubMed ID: 11556259
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ambiguous genitalia: an overview of 22 years experience and the diagnostic approach in the Pediatric Department, Siriraj Hospital.
    Nimkarn S; Likitmaskul S; Sangacharoenkit P; Pathomvanich A; Sawathiparnich P; Wacharasindhu S; Punnakanta L; Angsusingha K; Tuchinda C
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S496-505. PubMed ID: 12403225
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 46(10):560-5. PubMed ID: 11587068
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome.
    Melo KF; Latronico AC; Costa EM; Billerbeck AE; Mendonca BB; Arnhold IJ
    Hum Mutat; 1999 Oct; 14(4):353. PubMed ID: 10502786
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.