382 related articles for article (PubMed ID: 11530701)
21. Clinical, biochemical and morphologic diagnostic markers in an infant male pseudohermaphrodite patient with compound heterozygous mutations (G115D/R246W) in SRD5A2 gene.
Fernández-Cancio M; Rodó J; Andaluz P; Martínez de Osaba MJ; Rodríguez-Hierro F; Esteban C; Carrascosa A; Audí L
Horm Res; 2004; 62(5):259-64. PubMed ID: 15528927
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. A mutation c.C2812T in the androgen receptor gene resulting in Pro817Leu substitution may affect dimerization of the androgen receptor and result in androgen insensitivity syndrome.
Turek-Plewa J; Eckersdorf-Mastalerz A; Kaluzewski B; Helszer Z; Trzeciak WH
Fertil Steril; 2006 Jun; 85(6):1822.e1-4. PubMed ID: 16759930
[TBL] [Abstract][Full Text] [Related]
24. [From gene to disease; androgen receptor gene, androgen insensitivity syndrome, and spinal and bulbar muscle atrophy].
Boehmer AL; Brinkmann AO; Niermeijer MF; Halley DJ; Drop SL
Ned Tijdschr Geneeskd; 2001 Dec; 145(48):2326-8. PubMed ID: 11766302
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Clinical and molecular aspects of androgen insensitivity.
Hiort O
Endocr Dev; 2013; 24():33-40. PubMed ID: 23392093
[TBL] [Abstract][Full Text] [Related]
27. [Intersexuality in childhood].
Knorr D
Med Klin; 1974 Nov; 69(44):1779-90. PubMed ID: 4614037
[No Abstract] [Full Text] [Related]
28. Case Report of Male Pseudohermaphroditism (Androgen Insensitivity Syndrome): Congenital Disorder of Sexual Differentiation.
Patel K; Dessi D; Trivedi S
J Assoc Physicians India; 2023 Jan; 71(1):1. PubMed ID: 37116050
[TBL] [Abstract][Full Text] [Related]
29. Phenotype, hormonal profile and genotype of subjects with partial androgen insensitivity syndrome: report of a family with four adult males and one child with disorder of sexual differentiation.
Kulshreshtha B; Philibert P; Eunice M; Audran F; Paris F; Khurana ML; Ammini AC; Charles S
Andrologia; 2009 Aug; 41(4):257-63. PubMed ID: 19601939
[TBL] [Abstract][Full Text] [Related]
30. [Intersexuality: gonadal dysgenesis and testicular feminization].
Schweikert HU
Gynakologe; 1995 Feb; 28(1):17-26. PubMed ID: 7705711
[No Abstract] [Full Text] [Related]
31. Identification of a mutant allele of the androgen receptor gene in a family with androgen insensitivity syndrome: detection of carriers and prenatal diagnosis.
Fogu G; Bertini V; Dessole S; Bandiera P; Campus PM; Capobianco G; Sanna R; Soro G; Montella A
Arch Gynecol Obstet; 2004 May; 269(4):266-9. PubMed ID: 12898143
[TBL] [Abstract][Full Text] [Related]
32. Correlation between genotype, phenotype and sex of rearing in 111 patients with partial androgen insensitivity syndrome.
Deeb A; Mason C; Lee YS; Hughes IA
Clin Endocrinol (Oxf); 2005 Jul; 63(1):56-62. PubMed ID: 15963062
[TBL] [Abstract][Full Text] [Related]
33. A novel nonsense mutation in the N-terminal domain of the androgen receptor gene causes complete androgen insensitivity syndrome.
Cai Z; Li ZS; Liu XY
J Obstet Gynaecol; 2012 Oct; 32(7):707-8. PubMed ID: 22943730
[No Abstract] [Full Text] [Related]
34. Pseudovaginal perineoscrotal hypospadias: genetic heterogeneity.
Keenan BS
Urol Clin North Am; 1980 Jun; 7(2):393-407. PubMed ID: 6105737
[TBL] [Abstract][Full Text] [Related]
35. Undervirilization in XY newborns may hide a 5α-reductase deficiency: report of three new SRD5A2 gene mutations.
Maimoun L; Philibert P; Cammas B; Audran F; Pienkowski C; Kurtz F; Heinrich C; Cartigny M; Sultan C
Int J Androl; 2010 Dec; 33(6):841-7. PubMed ID: 20132346
[TBL] [Abstract][Full Text] [Related]
36. Androgen insensitivity syndrome (or Morris syndrome) and other associated pathologies.
Dell'Edera D; Malvasi A; Vitullo E; Epifania AA; Tinelli A; Laterza F; Novelli A; Pacella E; Mazzone E; Novelli G
Eur Rev Med Pharmacol Sci; 2010 Nov; 14(11):947-57. PubMed ID: 21284344
[TBL] [Abstract][Full Text] [Related]
37. Phenotypic diversity and testosterone-induced normalization of mutant L712F androgen receptor function in a kindred with androgen insensitivity.
Holterhus PM; Sinnecker GH; Hiort O
J Clin Endocrinol Metab; 2000 Sep; 85(9):3245-50. PubMed ID: 10999816
[TBL] [Abstract][Full Text] [Related]
38. Complete androgen insensitivity syndrome: clinical and anatomopathological findings in 23 patients.
Alvarez-Nava F; Gonzalez S; Soto M; Martinez C; Prieto M
Genet Couns; 1997; 8(1):7-12. PubMed ID: 9101272
[TBL] [Abstract][Full Text] [Related]
39. [Complete androgen insensitivity syndrome: diagnosis and clinical characteristics].
Solari A; Groisman B; Bidondo MP; Cinca C; Alba L
Arch Argent Pediatr; 2008 Jun; 106(3):265-8. PubMed ID: 18695842
[TBL] [Abstract][Full Text] [Related]
40. Endocrinological problems in malformation of the male genitalia.
Glatzl J
Prog Pediatr Surg; 1984; 17():1-10. PubMed ID: 6425967
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
