Detalhe da pesquisa
1.
GnRH stimulation testing and serum inhibin B in males: insufficient specificity for discriminating between congenital hypogonadotropic hypogonadism from constitutional delay of growth and puberty.
Hum Reprod
; 35(10): 2312-2322, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32862222
2.
Prevalence of KISS1 Receptor mutations in a series of 603 patients with normosmic congenital hypogonadotrophic hypogonadism and characterization of novel mutations: a single-centre study.
Hum Reprod
; 31(6): 1363-74, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27094476
3.
Mitotane for 21-hydroxylase deficiency in an infertile man.
N Engl J Med
; 371(21): 2042-4, 2014 Nov 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25409392
4.
Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life.
Orphanet J Rare Dis
; 10: 71, 2015 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26051373
5.
Terapia hormonal en persona transgénero según world professional association for transgender health (WPATH) () y guías clinicas de la endocrine society. () / Hormone therapy in transgender person according to world professional association for transgender health (WPATH) and clinical guidelines of the endocrine society
Rev. chil. obstet. ginecol. (En línea)
; 83(4): 426-441, 2018. tab
Artigo
em Espanhol
| LILACS | ID: biblio-978115
6.
Terapia hormonal en la transición femenino a masculino (ftm), androgénica, para trans masculino o para hombre transgénero / Hormone Therapy in Female to Male Transition (FTM), Androgenic, Trans Male, or Transgender Male
Rev. chil. obstet. ginecol. (En línea)
; 83(3): 318-328, jun. 2018. tab
Artigo
em Espanhol
| LILACS | ID: biblio-959521