537 related articles for article (PubMed ID: 20207726)
1. 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]
2. 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]
3. [GnRH deficiency: new insights from genetics].
Kottler ML; Hamel A; Malville E; Richard N
J Soc Biol; 2004; 198(1):80-7. PubMed ID: 15146960
[TBL] [Abstract][Full Text] [Related]
4. [Congenital hypogonadotropic hypogonadism and Kallmann syndrome in males].
Ghervan C; Young J
Presse Med; 2014 Feb; 43(2):152-61. PubMed ID: 24456696
[TBL] [Abstract][Full Text] [Related]
5. TAC3 and TACR3 defects cause hypothalamic congenital hypogonadotropic hypogonadism in humans.
Young J; Bouligand J; Francou B; Raffin-Sanson ML; Gaillez S; Jeanpierre M; Grynberg M; Kamenicky P; Chanson P; Brailly-Tabard S; Guiochon-Mantel A
J Clin Endocrinol Metab; 2010 May; 95(5):2287-95. PubMed ID: 20194706
[TBL] [Abstract][Full Text] [Related]
6. GnRH receptor and GPR54 inactivation in isolated gonadotropic deficiency.
de Roux N
Best Pract Res Clin Endocrinol Metab; 2006 Dec; 20(4):515-28. PubMed ID: 17161329
[TBL] [Abstract][Full Text] [Related]
7. Genetics defects in GNRH1: a paradigm of hypothalamic congenital gonadotropin deficiency.
Bouligand J; Ghervan C; Trabado S; Brailly-Tabard S; Guiochon-Mantel A; Young J
Brain Res; 2010 Dec; 1364():3-9. PubMed ID: 20887715
[TBL] [Abstract][Full Text] [Related]
8. 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.
Francou B; Paul C; Amazit L; Cartes A; Bouvattier C; Albarel F; Maiter D; Chanson P; Trabado S; Brailly-Tabard S; Brue T; Guiochon-Mantel A; Young J; Bouligand J
Hum Reprod; 2016 Jun; 31(6):1363-74. PubMed ID: 27094476
[TBL] [Abstract][Full Text] [Related]
9. Isolated gonadotropic deficiency with and without anosmia: a developmental defect or a neuroendocrine regulation abnormality of the gonadotropic axis.
de Roux N
Horm Res; 2005; 64 Suppl 2():48-55. PubMed ID: 16286771
[TBL] [Abstract][Full Text] [Related]
10. Kallmann's syndrome: a comparison of the reproductive phenotypes in men carrying KAL1 and FGFR1/KAL2 mutations.
Salenave S; Chanson P; Bry H; Pugeat M; Cabrol S; Carel JC; Murat A; Lecomte P; Brailly S; Hardelin JP; Dodé C; Young J
J Clin Endocrinol Metab; 2008 Mar; 93(3):758-63. PubMed ID: 18160472
[TBL] [Abstract][Full Text] [Related]
11. The complex genetic basis of congenital hypogonadotropic hypogonadism.
Vezzoli V; Duminuco P; Bassi I; Guizzardi F; Persani L; Bonomi M
Minerva Endocrinol; 2016 Jun; 41(2):223-39. PubMed ID: 26934720
[TBL] [Abstract][Full Text] [Related]
12. Approach to the male patient with congenital hypogonadotropic hypogonadism.
Young J
J Clin Endocrinol Metab; 2012 Mar; 97(3):707-18. PubMed ID: 22392951
[TBL] [Abstract][Full Text] [Related]
13. [Clinical and molecular genetic features of cases of isolated hypogonadotropic hypogonadism, associated with defects in
Makretskaya NA; Gerasimova MV; Vasilyev EV; Zubkova NA; Kalinchenko NY; Kolodkina AA; Petrov VM; Pogoda TV; Panova AV; Frolova EB; Poliakov AV; Tiulpakov AN
Probl Endokrinol (Mosk); 2021 May; 67(3):62-67. PubMed ID: 34297503
[TBL] [Abstract][Full Text] [Related]
14. GNRHR-related central hypogonadism with spontaneous recovery - case report.
Šmigoc Schweiger D; Davidović Povše M; Trebušak Podkrajšek K; Battelino T; Avbelj Stefanija M
Ital J Pediatr; 2022 Nov; 48(1):184. PubMed ID: 36371229
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Genetic insights into human isolated gonadotropin deficiency.
Trarbach EB; Silveira LG; Latronico AC
Pituitary; 2007; 10(4):381-91. PubMed ID: 17624596
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. GnRH receptor mutations in isolated gonadotropic deficiency.
Chevrier L; Guimiot F; de Roux N
Mol Cell Endocrinol; 2011 Oct; 346(1-2):21-8. PubMed ID: 21645587
[TBL] [Abstract][Full Text] [Related]
19. [Clinical and molecular aspects of congenital isolated hypogonadotropic hypogonadism].
Tusset C; Trarbach EB; Silveira LF; Beneduzzi D; Montenegro L; Latronico AC
Arq Bras Endocrinol Metabol; 2011 Nov; 55(8):501-11. PubMed ID: 22218430
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]