420 related articles for article (PubMed ID: 29280744)
1. Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism.
Topaloğlu AK
J Clin Res Pediatr Endocrinol; 2017 Dec; 9(Suppl 2):113-122. PubMed ID: 29280744
[TBL] [Abstract][Full Text] [Related]
2. Genetics of Hypogonadotropic Hypogonadism.
Topaloglu AK; Kotan LD
Endocr Dev; 2016; 29():36-49. PubMed ID: 26680571
[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. 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]
5. 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]
6. Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations.
Akkuş G; Kotan LD; Durmaz E; Mengen E; Turan İ; Ulubay A; Gürbüz F; Yüksel B; Tetiker T; Topaloğlu AK
J Clin Res Pediatr Endocrinol; 2017 Jun; 9(2):95-100. PubMed ID: 28008864
[TBL] [Abstract][Full Text] [Related]
7. Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
Kim HG; Kurth I; Lan F; Meliciani I; Wenzel W; Eom SH; Kang GB; Rosenberger G; Tekin M; Ozata M; Bick DP; Sherins RJ; Walker SL; Shi Y; Gusella JF; Layman LC
Am J Hum Genet; 2008 Oct; 83(4):511-9. PubMed ID: 18834967
[TBL] [Abstract][Full Text] [Related]
8. Genotypic and phenotypic spectra of FGFR1, FGF8, and FGF17 mutations in a Chinese cohort with idiopathic hypogonadotropic hypogonadism.
Men M; Wu J; Zhao Y; Xing X; Jiang F; Zheng R; Li JD
Fertil Steril; 2020 Jan; 113(1):158-166. PubMed ID: 31748124
[TBL] [Abstract][Full Text] [Related]
9. Novel FGFR1 mutations in Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: evidence for the involvement of an alternatively spliced isoform.
Gonçalves C; Bastos M; Pignatelli D; Borges T; Aragüés JM; Fonseca F; Pereira BD; Socorro S; Lemos MC
Fertil Steril; 2015 Nov; 104(5):1261-7.e1. PubMed ID: 26277103
[TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular features of idiopathic hypogonadotropic hypogonadism in Taiwan: A single center experience.
Cho CY; Tsai WY; Lee CT; Liu SY; Huang SY; Chien YH; Hwu WL; Lee NC; Tung YC
J Formos Med Assoc; 2022 Jan; 121(1 Pt 1):218-226. PubMed ID: 33775534
[TBL] [Abstract][Full Text] [Related]
11. Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism.
Stamou MI; Georgopoulos NA
Metabolism; 2018 Sep; 86():124-134. PubMed ID: 29108899
[TBL] [Abstract][Full Text] [Related]
12. The genetics of idiopathic hypogonadotropic hypogonadism:unraveling the biology of human sexual development.
Bhangoo A; Jacobson-Dickman E
Pediatr Endocrinol Rev; 2009 Mar; 6(3):395-404. PubMed ID: 19396025
[TBL] [Abstract][Full Text] [Related]
13. The role of prior pubertal development, biochemical markers of testicular maturation, and genetics in elucidating the phenotypic heterogeneity of idiopathic hypogonadotropic hypogonadism.
Pitteloud N; Hayes FJ; Boepple PA; DeCruz S; Seminara SB; MacLaughlin DT; Crowley WF
J Clin Endocrinol Metab; 2002 Jan; 87(1):152-60. PubMed ID: 11788640
[TBL] [Abstract][Full Text] [Related]
14. CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism.
Turan I; Hutchins BI; Hacihamdioglu B; Kotan LD; Gurbuz F; Ulubay A; Mengen E; Yuksel B; Wray S; Topaloglu AK
J Clin Endocrinol Metab; 2017 Jun; 102(6):1816-1825. PubMed ID: 28324054
[TBL] [Abstract][Full Text] [Related]
15. Prevalence and Phenotypic Effects of Copy Number Variants in Isolated Hypogonadotropic Hypogonadism.
Stamou MI; Brand H; Wang M; Wong I; Lippincott MF; Plummer L; Crowley WF; Talkowski M; Seminara S; Balasubramanian R
J Clin Endocrinol Metab; 2022 Jul; 107(8):2228-2242. PubMed ID: 35574646
[TBL] [Abstract][Full Text] [Related]
16. Spectrum of phenotype and genotype of congenital isolated hypogonadotropic hypogonadism in Asian Indians.
Nair S; Jadhav S; Lila A; Jagtap V; Bukan A; Pandit R; Ekbote A; Dharmalingam M; Kumar P; Kalra P; Gandhi P; Walia R; Sankhe S; Raghavan V; Shivane V; Menon P; Bandgar T; Shah N
Clin Endocrinol (Oxf); 2016 Jul; 85(1):100-9. PubMed ID: 26708526
[TBL] [Abstract][Full Text] [Related]
17. Mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism.
Zhou C; Niu Y; Xu H; Li Z; Wang T; Yang W; Wang S; Wang DW; Liu J
Fertil Steril; 2018 Aug; 110(3):486-495.e5. PubMed ID: 30098700
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.
Pitteloud N; Quinton R; Pearce S; Raivio T; Acierno J; Dwyer A; Plummer L; Hughes V; Seminara S; Cheng YZ; Li WP; Maccoll G; Eliseenkova AV; Olsen SK; Ibrahimi OA; Hayes FJ; Boepple P; Hall JE; Bouloux P; Mohammadi M; Crowley W
J Clin Invest; 2007 Feb; 117(2):457-63. PubMed ID: 17235395
[TBL] [Abstract][Full Text] [Related]
20. Reproductive Phenotypes and Genotypes in Men With IHH.
Dwyer AA; Stamou MI; Anghel E; Hornstein S; Chen D; Salnikov KB; McDonald IR; Plummer L; Seminara SB; Balasubramanian R
J Clin Endocrinol Metab; 2023 Mar; 108(4):897-908. PubMed ID: 36268624
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
