BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

268 related articles for article (PubMed ID: 35090434)

  • 1. 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]  

  • 2. 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]  

  • 3. [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]  

  • 4. 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]  

  • 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. 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]  

  • 7. Clinical Manifestations, Genetic Variants and Therapeutic Evaluation in Sporadic Chinese Patients with Idiopathic Hypogonadotropic Hypogonadism.
    He D; Sun H; Zhang M; Li Y; Liu F; Zhang Y; He M; Ban B
    Int J Gen Med; 2023; 16():4429-4439. PubMed ID: 37799300
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Clinical and molecular features of 40 Chinese patients with idiopathic hypogonadotropic hypogonadism.
    Wang Y; Jiang W; Xia X
    Transl Androl Urol; 2023 Sep; 12(9):1397-1407. PubMed ID: 37814704
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. The Clinical and Genetic Characteristics in Children with Idiopathic Hypogonadotropin Hypogonadism.
    Zhou Q; Sheng W; Yang S; Zou C
    J Oncol; 2022; 2022():7973726. PubMed ID: 36245975
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Multiplex ligation dependent probe amplification analysis of KAL1, GNRH1, GNRHR, PROK2 and PROKR2 in male patients with idiopathic hypogonadotropic hypogonadism.
    Basaran Y; Bolu E; Unal HU; Sagkan RI; Taslipinar A; Ozgurtas T; Musabak U
    Endokrynol Pol; 2013; 64(4):285-92. PubMed ID: 24002956
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes: pathophysiology and genotype-phenotype correlations.
    Sarfati J; Dodé C; Young J
    Front Horm Res; 2010; 39():121-132. PubMed ID: 20389090
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Oligogenic Inheritance Underlying Incomplete Penetrance of
    Mkaouar R; Abdallah LCB; Naouali C; Lahbib S; Turki Z; Elouej S; Bouyacoub Y; Somai M; Mcelreavey K; Bashamboo A; Abdelhak S; Messaoud O
    Front Genet; 2021; 12():665174. PubMed ID: 34539727
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.