284 related articles for article (PubMed ID: 27094476)
1. 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]
2. Similarities and differences in the reproductive phenotypes of women with congenital hypogonadotrophic hypogonadism caused by GNRHR mutations and women with polycystic ovary syndrome.
Maione L; Fèvre A; Nettore IC; Manilall A; Francou B; Trabado S; Bouligand J; Guiochon-Mantel A; Delemer B; Flanagan CA; Macchia PE; Millar RP; Young J
Hum Reprod; 2019 Jan; 34(1):137-147. PubMed ID: 30476149
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Two families with normosmic congenital hypogonadotropic hypogonadism and biallelic mutations in KISS1R (KISS1 receptor): clinical evaluation and molecular characterization of a novel mutation.
Brioude F; Bouligand J; Francou B; Fagart J; Roussel R; Viengchareun S; Combettes L; Brailly-Tabard S; Lombès M; Young J; Guiochon-Mantel A
PLoS One; 2013; 8(1):e53896. PubMed ID: 23349759
[TBL] [Abstract][Full Text] [Related]
5. Regional genotypic variations in normosmic congenital hypogonadotropic hypogonadism: our experience and systematic review.
Patil VA; Lila AR; Shah N; Arya S; Ekbote AV; Sarathi V; Shah R; Jadhav SS; Memon SS; Bandgar T
Pituitary; 2022 Jun; 25(3):444-453. PubMed ID: 35133534
[TBL] [Abstract][Full Text] [Related]
6. Genetics of ncHH: from a peculiar inheritance of a novel GNRHR mutation to a comprehensive review of the literature.
Cioppi F; Riera-Escamilla A; Manilall A; Guarducci E; Todisco T; Corona G; Colombo F; Bonomi M; Flanagan CA; Krausz C
Andrology; 2019 Jan; 7(1):88-101. PubMed ID: 30575316
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism.
Gürbüz F; Kotan LD; Mengen E; Şıklar Z; Berberoğlu M; Dökmetaş S; Kılıçlı MF; Güven A; Kirel B; Saka N; Poyrazoğlu Ş; Cesur Y; Doğan M; Özen S; Özbek MN; Demirbilek H; Kekil MB; Temiz F; Önenli Mungan N; Yüksel B; Topaloğlu AK
J Clin Res Pediatr Endocrinol; 2012 Sep; 4(3):121-6. PubMed ID: 22766261
[TBL] [Abstract][Full Text] [Related]
9. GnRH stimulation testing and serum inhibin B in males: insufficient specificity for discriminating between congenital hypogonadotropic hypogonadism from constitutional delay of growth and puberty.
Mosbah H; Bouvattier C; Maione L; Trabado S; De Filippo G; Cartes A; Donzeau A; Chanson P; Brailly-Tabard S; Dwyer AA; Coutant R; Young J
Hum Reprod; 2020 Oct; 35(10):2312-2322. PubMed ID: 32862222
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel
Nalbantoğlu Ö; Arslan G; Köprülü Ö; Hazan F; Gürsoy S; Özkan B
J Clin Res Pediatr Endocrinol; 2019 Nov; 11(4):444-448. PubMed ID: 30905142
[TBL] [Abstract][Full Text] [Related]
12. Complete Kisspeptin Receptor Inactivation Does Not Impede Exogenous GnRH-Induced LH Surge in Humans.
Hugon-Rodin J; Yoshii K; Lahlou N; Flandrin J; Gompel A; de Roux N
J Clin Endocrinol Metab; 2018 Dec; 103(12):4482-4490. PubMed ID: 30124894
[TBL] [Abstract][Full Text] [Related]
13.
Gonçalves CI; Aragüés JM; Bastos M; Barros L; Vicente N; Carvalho D; Lemos MC
Endocr Connect; 2017 Aug; 6(6):360-366. PubMed ID: 28611058
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood.
Gianetti E; Tusset C; Noel SD; Au MG; Dwyer AA; Hughes VA; Abreu AP; Carroll J; Trarbach E; Silveira LF; Costa EM; de Mendonça BB; de Castro M; Lofrano A; Hall JE; Bolu E; Ozata M; Quinton R; Amory JK; Stewart SE; Arlt W; Cole TR; Crowley WF; Kaiser UB; Latronico AC; Seminara SB
J Clin Endocrinol Metab; 2010 Jun; 95(6):2857-67. PubMed ID: 20332248
[TBL] [Abstract][Full Text] [Related]
16. Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism.
Moalla M; Hadj Kacem F; Al-Mutery AF; Mahfood M; Mejdoub-Rekik N; Abid M; Mnif-Feki M; Hadj Kacem H
J Assist Reprod Genet; 2019 Jun; 36(6):1273-1280. PubMed ID: 31073722
[TBL] [Abstract][Full Text] [Related]
17. Whole Exome Sequencing Revealed a Novel Nonsense Variant in the GNRHR Gene Causing Normosmic Hypogonadotropic Hypogonadism in a Pakistani Family.
Hussain HMJ; Murtaza G; Jiang X; Khan R; Khan M; Kakakhel MBS; Khan T; Wahab F; Zhang H; Zhang Y; Khan MB; Ahmed P; Ma H; Xu Z
Horm Res Paediatr; 2019; 91(1):9-16. PubMed ID: 30947225
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Expression of neurokinin B/NK3 receptor and kisspeptin/KISS1 receptor in human granulosa cells.
García-Ortega J; Pinto FM; Fernández-Sánchez M; Prados N; Cejudo-Román A; Almeida TA; Hernández M; Romero M; Tena-Sempere M; Candenas L
Hum Reprod; 2014 Dec; 29(12):2736-46. PubMed ID: 25316443
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
