233 related articles for article (PubMed ID: 22031817)
21. Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders.
Tusset C; Noel SD; Trarbach EB; Silveira LF; Jorge AA; Brito VN; Cukier P; Seminara SB; Mendonça BB; Kaiser UB; Latronico AC
Arq Bras Endocrinol Metabol; 2012 Dec; 56(9):646-52. PubMed ID: 23329188
[TBL] [Abstract][Full Text] [Related]
22. Genetics of isolated hypogonadotropic hypogonadism: role of GnRH receptor and other genes.
Beate K; Joseph N; Nicolas de R; Wolfram K
Int J Endocrinol; 2012; 2012():147893. PubMed ID: 22229029
[TBL] [Abstract][Full Text] [Related]
23. The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
Quaynor SD; Kim HG; Cappello EM; Williams T; Chorich LP; Bick DP; Sherins RJ; Layman LC
Fertil Steril; 2011 Dec; 96(6):1424-1430.e6. PubMed ID: 22035731
[TBL] [Abstract][Full Text] [Related]
24. The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism.
Bianco SD; Kaiser UB
Nat Rev Endocrinol; 2009 Oct; 5(10):569-76. PubMed ID: 19707180
[TBL] [Abstract][Full Text] [Related]
25. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.
Abreu AP; Trarbach EB; de Castro M; Frade Costa EM; Versiani B; Matias Baptista MT; Garmes HM; Mendonca BB; Latronico AC
J Clin Endocrinol Metab; 2008 Oct; 93(10):4113-8. PubMed ID: 18682503
[TBL] [Abstract][Full Text] [Related]
26. Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype-phenotype relationships.
Brioude F; Bouligand J; Trabado S; Francou B; Salenave S; Kamenicky P; Brailly-Tabard S; Chanson P; Guiochon-Mantel A; Young J
Eur J Endocrinol; 2010 May; 162(5):835-51. PubMed ID: 20207726
[TBL] [Abstract][Full Text] [Related]
27. Biallelic PROKR2 variants and congenital hypogonadotropic hypogonadism: a case report and a literature review.
Sugisawa C; Taniyama M; Sato T; Takahashi Y; Hasegawa T; Narumi S
Endocr J; 2022 Jul; 69(7):831-838. PubMed ID: 35236788
[TBL] [Abstract][Full Text] [Related]
28. R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
Maione L; Albarel F; Bouchard P; Gallant M; Flanagan CA; Bobe R; Cohen-Tannoudji J; Pivonello R; Colao A; Brue T; Millar RP; Lombes M; Young J; Guiochon-Mantel A; Bouligand J
PLoS One; 2013; 8(7):e69616. PubMed ID: 23936060
[TBL] [Abstract][Full Text] [Related]
29. Genetics of Hypogonadotropic Hypogonadism.
Topaloglu AK; Kotan LD
Endocr Dev; 2016; 29():36-49. PubMed ID: 26680571
[TBL] [Abstract][Full Text] [Related]
30. Genetics basis for GnRH-dependent pubertal disorders in humans.
Silveira LF; Trarbach EB; Latronico AC
Mol Cell Endocrinol; 2010 Aug; 324(1-2):30-8. PubMed ID: 20188792
[TBL] [Abstract][Full Text] [Related]
31. Responsiveness to a physiological regimen of GnRH therapy and relation to genotype in women with isolated hypogonadotropic hypogonadism.
Abel BS; Shaw ND; Brown JM; Adams JM; Alati T; Martin KA; Pitteloud N; Seminara SB; Plummer L; Pignatelli D; Crowley WF; Welt CK; Hall JE
J Clin Endocrinol Metab; 2013 Feb; 98(2):E206-16. PubMed ID: 23341491
[TBL] [Abstract][Full Text] [Related]
32. Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.
Barraud S; Delemer B; Poirsier-Violle C; Bouligand J; Mérol JC; Grange F; Higel-Chaufour B; Decoudier B; Zalzali M; Dwyer AA; Acierno JS; Pitteloud N; Millar RP; Young J
Neuroendocrinology; 2021; 111(1-2):99-114. PubMed ID: 32074614
[TBL] [Abstract][Full Text] [Related]
33. Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism.
Aoyama K; Mizuno H; Tanaka T; Togawa T; Negishi Y; Ohashi K; Hori I; Izawa M; Hamajima T; Saitoh S
J Pediatr Endocrinol Metab; 2017 Oct; 30(10):1111-1118. PubMed ID: 28915117
[TBL] [Abstract][Full Text] [Related]
34. Neurokinin B signalling in human puberty.
Topaloglu AK; Kotan LD; Yuksel B
J Neuroendocrinol; 2010 Jul; 22(7):765-70. PubMed ID: 20456599
[TBL] [Abstract][Full Text] [Related]
35. Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience.
Shin SJ; Sul Y; Kim JH; Cho JH; Kim GH; Kim JH; Choi JH; Yoo HW
Ann Pediatr Endocrinol Metab; 2015 Mar; 20(1):27-33. PubMed ID: 25883924
[TBL] [Abstract][Full Text] [Related]
36. Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes.
Valdes-Socin H; Rubio Almanza M; Tomé Fernández-Ladreda M; Debray FG; Bours V; Beckers A
Front Endocrinol (Lausanne); 2014; 5():109. PubMed ID: 25071724
[TBL] [Abstract][Full Text] [Related]
37. TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction.
Topaloglu AK; Reimann F; Guclu M; Yalin AS; Kotan LD; Porter KM; Serin A; Mungan NO; Cook JR; Imamoglu S; Akalin NS; Yuksel B; O'Rahilly S; Semple RK
Nat Genet; 2009 Mar; 41(3):354-358. PubMed ID: 19079066
[TBL] [Abstract][Full Text] [Related]
38. GnRH receptor gene mutations in adolescents and young adults presenting with signs of partial gonadotropin deficiency.
Hietamäki J; Hero M; Holopainen E; Känsäkoski J; Vaaralahti K; Iivonen AP; Miettinen PJ; Raivio T
PLoS One; 2017; 12(11):e0188750. PubMed ID: 29182666
[TBL] [Abstract][Full Text] [Related]
39. [Hypogonadotropic hypogonadism: new aspects in the regulation of hypothalamic-pituitary-gonadal axis].
Brioude F; Bouvattier CE; Lombès M
Ann Endocrinol (Paris); 2010 Sep; 71 Suppl 1():S33-41. PubMed ID: 21237329
[TBL] [Abstract][Full Text] [Related]
40. Additional mutation in
Ichioka K; Yoshikawa T; Kimura H; Saito R
BMJ Case Rep; 2024 Jan; 17(1):. PubMed ID: 38272512
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
