169 related articles for article (PubMed ID: 21664240)
1. Isolated cryptorchidism: no evidence for involvement of genes underlying isolated hypogonadotropic hypogonadism.
Laitinen EM; Tommiska J; Virtanen HE; Oehlandt H; Koivu R; Vaaralahti K; Toppari J; Raivio T
Mol Cell Endocrinol; 2011 Jul; 341(1-2):35-8. PubMed ID: 21664240
[TBL] [Abstract][Full Text] [Related]
2. The role of gene defects underlying isolated hypogonadotropic hypogonadism in patients with constitutional delay of growth and puberty.
Vaaralahti K; Wehkalampi K; Tommiska J; Laitinen EM; Dunkel L; Raivio T
Fertil Steril; 2011 Jun; 95(8):2756-8. PubMed ID: 21292259
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Complex genetics in idiopathic hypogonadotropic hypogonadism.
Pitteloud N; Durrani S; Raivio T; Sykiotis GP
Front Horm Res; 2010; 39():142-153. PubMed ID: 20389092
[TBL] [Abstract][Full Text] [Related]
5. Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.
Canto P; Munguía P; Söderlund D; Castro JJ; Méndez JP
J Androl; 2009; 30(1):41-5. PubMed ID: 18723471
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Idiopathic hypogonadotropic hypogonadism in a mother and her monozygotic twins born after a single embryo transfer.
Laitinen EM; Tommiska J; Dunkel L; Sankilampi U; Vaaralahti K; Raivio T
Fertil Steril; 2010 Apr; 93(6):2074.e13-6. PubMed ID: 20079901
[TBL] [Abstract][Full Text] [Related]
8. Congenital hypogonadotropic hypogonadism in females: clinical spectrum, evaluation and genetics.
Bry-Gauillard H; Trabado S; Bouligand J; Sarfati J; Francou B; Salenave S; Chanson P; Brailly-Tabard S; Guiochon-Mantel A; Young J
Ann Endocrinol (Paris); 2010 May; 71(3):158-62. PubMed ID: 20363464
[TBL] [Abstract][Full Text] [Related]
9. Genetics of congenital hypogonadotropic hypogonadism in Denmark.
Tommiska J; Känsäkoski J; Christiansen P; Jørgensen N; Lawaetz JG; Juul A; Raivio T
Eur J Med Genet; 2014 Jul; 57(7):345-8. PubMed ID: 24732674
[TBL] [Abstract][Full Text] [Related]
10. The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.
Hardelin JP; Dodé C
Sex Dev; 2008; 2(4-5):181-93. PubMed ID: 18987492
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Triallelic digenic mutation in the prokineticin 2 and GNRH receptor genes in two brothers with normosmic congenital hypogonadotropic hypogonadism.
Méndez JP; Zenteno JC; Coronel A; Soriano-Ursúa MA; Valencia-Villalvazo EY; Soderlund D; Coral-Vázquez RM; Canto P
Endocr Res; 2015; 40(3):166-71. PubMed ID: 25531638
[TBL] [Abstract][Full Text] [Related]
13. Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism.
Bhagavath B; Podolsky RH; Ozata M; Bolu E; Bick DP; Kulharya A; Sherins RJ; Layman LC
Fertil Steril; 2006 Mar; 85(3):706-13. PubMed ID: 16500342
[TBL] [Abstract][Full Text] [Related]
14. The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
Semple RK; Topaloglu AK
Clin Endocrinol (Oxf); 2010 Apr; 72(4):427-35. PubMed ID: 19719764
[TBL] [Abstract][Full Text] [Related]
15. Normosmic congenital hypogonadotropic hypogonadism due to TAC3/TACR3 mutations: characterization of neuroendocrine phenotypes and novel mutations.
Francou B; Bouligand J; Voican A; Amazit L; Trabado S; Fagart J; Meduri G; Brailly-Tabard S; Chanson P; Lecomte P; Guiochon-Mantel A; Young J
PLoS One; 2011; 6(10):e25614. PubMed ID: 22031817
[TBL] [Abstract][Full Text] [Related]
16. Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism.
Versiani BR; Trarbach E; Koenigkam-Santos M; Dos Santos AC; Elias LL; Moreira AC; Latronico AC; de Castro M
Clin Endocrinol (Oxf); 2007 Feb; 66(2):173-9. PubMed ID: 17223984
[TBL] [Abstract][Full Text] [Related]
17. Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum.
Cole LW; Sidis Y; Zhang C; Quinton R; Plummer L; Pignatelli D; Hughes VA; Dwyer AA; Raivio T; Hayes FJ; Seminara SB; Huot C; Alos N; Speiser P; Takeshita A; Van Vliet G; Pearce S; Crowley WF; Zhou QY; Pitteloud N
J Clin Endocrinol Metab; 2008 Sep; 93(9):3551-9. PubMed ID: 18559922
[TBL] [Abstract][Full Text] [Related]
18. Variants in congenital hypogonadotrophic hypogonadism genes identified in an Indonesian cohort of 46,XY under-virilised boys.
Ayers KL; Bouty A; Robevska G; van den Bergen JA; Juniarto AZ; Listyasari NA; Sinclair AH; Faradz SM
Hum Genomics; 2017 Feb; 11(1):1. PubMed ID: 28209183
[TBL] [Abstract][Full Text] [Related]
19. Reversible congenital hypogonadotropic hypogonadism in patients with CHD7, FGFR1 or GNRHR mutations.
Laitinen EM; Tommiska J; Sane T; Vaaralahti K; Toppari J; Raivio T
PLoS One; 2012; 7(6):e39450. PubMed ID: 22724017
[TBL] [Abstract][Full Text] [Related]
20. Role of sequence variations of the GnRH receptor and G protein-coupled receptor 54 gene in male idiopathic hypogonadotropic hypogonadism.
Lanfranco F; Gromoll J; von Eckardstein S; Herding EM; Nieschlag E; Simoni M
Eur J Endocrinol; 2005 Dec; 153(6):845-52. PubMed ID: 16322390
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]