357 related articles for article (PubMed ID: 23329762)
1. 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; 25(11-12):1145-51. PubMed ID: 23329762
[TBL] [Abstract][Full Text] [Related]
2. 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; 80(1):216-8. PubMed ID: 22608796
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Complete androgen insensitivity syndrome and discordant Müllerian remnants: two cases with novel mutation in the androgen receptor.
Güven A; Dursun F; Özkanlı S; Güçlüer B; Kuru Lİ
J Pediatr Endocrinol Metab; 2013; 26(9-10):909-14. PubMed ID: 23729616
[TBL] [Abstract][Full Text] [Related]
5. 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
[TBL] [Abstract][Full Text] [Related]
6. Sex-reversed phenotype in association with two novel mutations c.2494delA and c.T3004C in the ligand-binding domain of the androgen receptor gene.
Galani A; Sofocleous C; Karahaliou F; Papathanasiou A; Kitsiou-Tzeli S; Kalpini-Mavrou A
Fertil Steril; 2008 Nov; 90(5):2008.e1-4. PubMed ID: 18342859
[TBL] [Abstract][Full Text] [Related]
7. Androgen insensitivity syndrome.
Mendoza N; Motos MA
Gynecol Endocrinol; 2013 Jan; 29(1):1-5. PubMed ID: 22812659
[TBL] [Abstract][Full Text] [Related]
8. A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndrome.
Dörk T; Schnieders F; Jakubiczka S; Wieacker P; Schroeder-Kurth T; Schmidtke J
Hum Mutat; 1998; 11(4):337-9. PubMed ID: 9554754
[TBL] [Abstract][Full Text] [Related]
9. A novel Arg615Ser mutation of androgen receptor DNA-binding domain in three 46,XY sisters with complete androgen insensitivity syndrome and bilateral inguinal hernia.
Sharma V; Singh R; Thangaraj K; Jyothy A
Fertil Steril; 2011 Feb; 95(2):804.e19-21. PubMed ID: 20888558
[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. Genotype versus phenotype in families with androgen insensitivity syndrome.
Boehmer AL; Brinkmann O; Brüggenwirth H; van Assendelft C; Otten BJ; Verleun-Mooijman MC; Niermeijer MF; Brunner HG; Rouwé CW; Waelkens JJ; Oostdijk W; Kleijer WJ; van der Kwast TH; de Vroede MA; Drop SL
J Clin Endocrinol Metab; 2001 Sep; 86(9):4151-60. PubMed ID: 11549642
[TBL] [Abstract][Full Text] [Related]
12. A(870)E mutation of the androgen receptor gene in a patient with complete androgen insensitivity syndrome and Sertoli cell tumor.
Knoke I; Jakubiczka S; Ottersen T; Göppinger A; Wieacker P
Cancer Genet Cytogenet; 1997 Oct; 98(2):139-41. PubMed ID: 9332480
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Complete androgen insensitivity syndrome caused by a novel mutation in the ligand-binding domain of the androgen receptor: functional characterization.
Rosa S; Biason-Lauber A; Mongan NP; Navratil F; Schoenle EJ
J Clin Endocrinol Metab; 2002 Sep; 87(9):4378-82. PubMed ID: 12213902
[TBL] [Abstract][Full Text] [Related]
15. A novel E153X point mutation in the androgen receptor gene in a patient with complete androgen insensitivity syndrome.
Copelli SB; Lumbroso S; Audran F; Pellizzari EH; Heinrich JJ; Cigorraga SB; Sultan C; Chemes HE
Asian J Androl; 1999 Jun; 1(1-2):73-7. PubMed ID: 11225909
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. L712V mutation in the androgen receptor gene causes complete androgen insensitivity syndrome due to severe loss of androgen function.
Rajender S; Gupta NJ; Chakrabarty B; Singh L; Thangaraj K
Steroids; 2013 Dec; 78(12-13):1288-92. PubMed ID: 24055831
[TBL] [Abstract][Full Text] [Related]
18. [Male pseudohermaphroditism due to disorder of androgen receptor function].
Miyamoto J; Hasegawa Y
Nihon Rinsho; 2002 Feb; 60(2):367-72. PubMed ID: 11857928
[TBL] [Abstract][Full Text] [Related]
19. [Identification of a novel frameshift mutation of human androgen receptor gene in a patient featuring complete androgen insensitivity syndrome].
Xie JH; Qu JH; Xiao QZ; Zhou YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):99-101. PubMed ID: 23450491
[TBL] [Abstract][Full Text] [Related]
20. A novel androgen receptor mutation resulting in complete androgen insensitivity syndrome and bilateral Leydig cell hyperplasia.
Singh R; Shastry PK; Rasalkar AA; Singh L; Thangaraj K
J Androl; 2006; 27(4):510-6. PubMed ID: 16582414
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]