184 related articles for article (PubMed ID: 37798680)
1. Idiopathic hypogonadotropic hypogonadism caused by compound heterozygosity for two novel mutations in the GNRH1 gene: a case report.
Tian Q; Tang J; Wang L; Liu J; Li X; Cao Z; Tian Z
BMC Endocr Disord; 2023 Oct; 23(1):213. PubMed ID: 37798680
[TBL] [Abstract][Full Text] [Related]
2. GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadism.
Chan YM; de Guillebon A; Lang-Muritano M; Plummer L; Cerrato F; Tsiaras S; Gaspert A; Lavoie HB; Wu CH; Crowley WF; Amory JK; Pitteloud N; Seminara SB
Proc Natl Acad Sci U S A; 2009 Jul; 106(28):11703-8. PubMed ID: 19567835
[TBL] [Abstract][Full Text] [Related]
3. Clinical, hormonal, and genetic characteristics of 25 Chinese patients with idiopathic hypogonadotropic hypogonadism.
Liu Q; Yin X; Li P
BMC Endocr Disord; 2022 Jan; 22(1):30. PubMed ID: 35090434
[TBL] [Abstract][Full Text] [Related]
4. Isolated familial hypogonadotropic hypogonadism and a GNRH1 mutation.
Bouligand J; Ghervan C; Tello JA; Brailly-Tabard S; Salenave S; Chanson P; Lombès M; Millar RP; Guiochon-Mantel A; Young J
N Engl J Med; 2009 Jun; 360(26):2742-8. PubMed ID: 19535795
[TBL] [Abstract][Full Text] [Related]
5. Research on the variants of FGFR1 and CEP290 genes in idiopathic hypogonadotropin hypogonadism.
Wang SS; Zhao WY; Wu HX; Shu M; Yuan JX; Fang L; Xu C
Yi Chuan; 2022 Oct; 44(10):937-949. PubMed ID: 36384729
[TBL] [Abstract][Full Text] [Related]
6. Normosmic idiopathic hypogonadotropic hypogonadism due to a novel GNRH1 variant in two siblings.
Sagi SV; Joshi H; Whiles E; Hikmat M; Puthi VR; MacDougall J; Spiden SL; Fuller G; Park SM; Oyibo SO
Endocrinol Diabetes Metab Case Rep; 2020 Mar; 2020():. PubMed ID: 32134721
[TBL] [Abstract][Full Text] [Related]
7. Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.
Pitteloud N; Zhang C; Pignatelli D; Li JD; Raivio T; Cole LW; Plummer L; Jacobson-Dickman EE; Mellon PL; Zhou QY; Crowley WF
Proc Natl Acad Sci U S A; 2007 Oct; 104(44):17447-52. PubMed ID: 17959774
[TBL] [Abstract][Full Text] [Related]
8. [Children with idiopathic hypogonadotropic hypogonadism: clinical data analysis and mutations analysis of KAL1 and FGFR1 gene].
Qin M; Gong C; Qi Z; Wu D; Liu M; Gu Y; Cao B; Li W; Liang X
Zhonghua Er Ke Za Zhi; 2014 Dec; 52(12):942-7. PubMed ID: 25619354
[TBL] [Abstract][Full Text] [Related]
9. Homozygous p.R31H GNRH1 mutation and normosmic congenital hypogonadotropic hypogonadism in a patient and self-limited delayed puberty in his relatives.
Brachet C; Gernay C; Boros E; Soblet J; Vilain C; Heinrichs C
J Pediatr Endocrinol Metab; 2020 Sep; 33(9):1237-1240. PubMed ID: 32813678
[TBL] [Abstract][Full Text] [Related]
10. Functional Characteristics of Novel FGFR1 Mutations in Patients with Isolated Gonadotropin-Releasing Hormone Deficiency.
Choi JH; Oh A; Lee Y; Kim GH; Yoo HW
Exp Clin Endocrinol Diabetes; 2021 Jun; 129(6):457-463. PubMed ID: 32485746
[TBL] [Abstract][Full Text] [Related]
11. The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
Pedersen-White JR; Chorich LP; Bick DP; Sherins RJ; Layman LC
Mol Hum Reprod; 2008 Jun; 14(6):367-70. PubMed ID: 18463157
[TBL] [Abstract][Full Text] [Related]
12. Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism.
Kotan LD; Isik E; Turan I; Mengen E; Akkus G; Tastan M; Gurbuz F; Yuksel B; Topaloglu AK
Clin Genet; 2019 Feb; 95(2):320-324. PubMed ID: 30467832
[TBL] [Abstract][Full Text] [Related]
13. Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization.
Quinton R; Duke VM; Robertson A; Kirk JM; Matfin G; de Zoysa PA; Azcona C; MacColl GS; Jacobs HS; Conway GS; Besser M; Stanhope RG; Bouloux PM
Clin Endocrinol (Oxf); 2001 Aug; 55(2):163-74. PubMed ID: 11531922
[TBL] [Abstract][Full Text] [Related]
14. Reversal of idiopathic hypogonadotropic hypogonadism.
Raivio T; Falardeau J; Dwyer A; Quinton R; Hayes FJ; Hughes VA; Cole LW; Pearce SH; Lee H; Boepple P; Crowley WF; Pitteloud N
N Engl J Med; 2007 Aug; 357(9):863-73. PubMed ID: 17761590
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Molecular defects of the GnRH-receptor gene in Chinese patients with idiopathic hypogonadotropic hypogonadism and the severity of hypogonadism.
Fathi AK; Hu S; Fu X; Huang S; Liang Y; Ning Q; Luo X
J Pediatr Endocrinol Metab; 2012; 25(7-8):659-68. PubMed ID: 23155690
[TBL] [Abstract][Full Text] [Related]
17. Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice.
Falardeau J; Chung WC; Beenken A; Raivio T; Plummer L; Sidis Y; Jacobson-Dickman EE; Eliseenkova AV; Ma J; Dwyer A; Quinton R; Na S; Hall JE; Huot C; Alois N; Pearce SH; Cole LW; Hughes V; Mohammadi M; Tsai P; Pitteloud N
J Clin Invest; 2008 Aug; 118(8):2822-31. PubMed ID: 18596921
[TBL] [Abstract][Full Text] [Related]
18. Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadism.
Dai W; Li JD; Zhao Y; Wu J; Jiang F; Chen DN; Zheng R; Men M
Clin Genet; 2020 May; 97(5):696-703. PubMed ID: 32060892
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Congenital idiopathic hypogonadotropic hypogonadism: evidence of defects in the hypothalamus, pituitary, and testes.
Sykiotis GP; Hoang XH; Avbelj M; Hayes FJ; Thambundit A; Dwyer A; Au M; Plummer L; Crowley WF; Pitteloud N
J Clin Endocrinol Metab; 2010 Jun; 95(6):3019-27. PubMed ID: 20382682
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
