ALLMedicine™ Androgen Insensitivity Syndrome Center
Research & Reviews 439 results
https://doi.org/10.1016/j.fertnstert.2021.02.035
Fertility and Sterility; Blachman-Braun R, Gonzalez DC
Mar 22nd, 2021 - Using molecular genetics in complete androgen insensitivity syndrome: toward a more personalized medicine approach.|2021|Blachman-Braun R,Gonzalez DC,|
https://doi.org/10.1159/000514070
Sexual Development : Genetics, Molecular Biology, Evoluti... Lee SR
Mar 4th, 2021 - Androgen insensitivity syndrome (AIS) is a congenital condition characterized by a 46,XY karyotype but with a female phenotype caused by mutations in the androgen receptor gene located on the X chromosome. In patients with complete AIS (CAIS), pre...
https://doi.org/10.1016/j.fertnstert.2020.12.008
Fertility and Sterility; Zhang D, Yao F et. al.
Feb 19th, 2021 - To study the clinical characteristics and genetic basis of complete androgen insensitivity syndrome (CAIS) in patients from the People's Republic of China. CAIS patients with 46 XY karyotype produce male levels of androgens but present with female...
https://doi.org/10.1515/jpem-2008-210609
Journal of Pediatric Endocrinology & Metabolism : JPEM; Choi JH, Kim GH et. al.
Feb 18th, 2021 - The aim of this study was to assess the clinical and endocrinological features, and to analyze AR and SRD5A2 genes in patients with 46,XY disorders of sex development (DSD). This study included 20 patients from 19 families showing clinical feature...
https://doi.org/10.1016/j.jpag.2020.11.012
Journal of Pediatric and Adolescent Gynecology; Duranteau L, Rapp M et. al.
Nov 28th, 2020 - To evaluate the outcomes of genital surgery through participant's and observer's satisfaction with the anatomical and functional result. Multicenter cross-sectional study in 14 clinics in 6 European countries in 2014-2015. Seventy-one individuals ...
Clinicaltrials.gov 439 results
https://doi.org/10.1016/j.fertnstert.2021.02.035
Fertility and Sterility; Blachman-Braun R, Gonzalez DC
Mar 22nd, 2021 - Using molecular genetics in complete androgen insensitivity syndrome: toward a more personalized medicine approach.|2021|Blachman-Braun R,Gonzalez DC,|
https://doi.org/10.1159/000514070
Sexual Development : Genetics, Molecular Biology, Evoluti... Lee SR
Mar 4th, 2021 - Androgen insensitivity syndrome (AIS) is a congenital condition characterized by a 46,XY karyotype but with a female phenotype caused by mutations in the androgen receptor gene located on the X chromosome. In patients with complete AIS (CAIS), pre...
https://doi.org/10.1016/j.fertnstert.2020.12.008
Fertility and Sterility; Zhang D, Yao F et. al.
Feb 19th, 2021 - To study the clinical characteristics and genetic basis of complete androgen insensitivity syndrome (CAIS) in patients from the People's Republic of China. CAIS patients with 46 XY karyotype produce male levels of androgens but present with female...
https://doi.org/10.1515/jpem-2008-210609
Journal of Pediatric Endocrinology & Metabolism : JPEM; Choi JH, Kim GH et. al.
Feb 18th, 2021 - The aim of this study was to assess the clinical and endocrinological features, and to analyze AR and SRD5A2 genes in patients with 46,XY disorders of sex development (DSD). This study included 20 patients from 19 families showing clinical feature...
https://doi.org/10.1016/j.jpag.2020.11.012
Journal of Pediatric and Adolescent Gynecology; Duranteau L, Rapp M et. al.
Nov 28th, 2020 - To evaluate the outcomes of genital surgery through participant's and observer's satisfaction with the anatomical and functional result. Multicenter cross-sectional study in 14 clinics in 6 European countries in 2014-2015. Seventy-one individuals ...
