BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 36268624)

  • 1. 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]  

  • 2. 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]  

  • 3. The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.
    Oliveira LM; Seminara SB; Beranova M; Hayes FJ; Valkenburgh SB; Schipani E; Costa EM; Latronico AC; Crowley WF; Vallejo M
    J Clin Endocrinol Metab; 2001 Apr; 86(4):1532-8. PubMed ID: 11297579
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Reversible hypogonadotropic hypogonadism in men with the fertile eunuch/Pasqualini syndrome: A single-center natural history study.
    Dwyer AA; Stamou M; McDonald IR; Anghel E; Cox KH; Salnikov KB; Plummer L; Seminara SB; Balasubramanian R
    Front Endocrinol (Lausanne); 2022; 13():1054447. PubMed ID: 36407308
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The spectrum of abnormal patterns of gonadotropin-releasing hormone secretion in men with idiopathic hypogonadotropic hypogonadism: clinical and laboratory correlations.
    Spratt DI; Carr DB; Merriam GR; Scully RE; Rao PN; Crowley WF
    J Clin Endocrinol Metab; 1987 Feb; 64(2):283-91. PubMed ID: 3098771
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.
    Pitteloud N; Meysing A; Quinton R; Acierno JS; Dwyer AA; Plummer L; Fliers E; Boepple P; Hayes F; Seminara S; Hughes VA; Ma J; Bouloux P; Mohammadi M; Crowley WF
    Mol Cell Endocrinol; 2006 Jul; 254-255():60-9. PubMed ID: 16764984
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Prevalence of pathogenic variants and digenic disease in patients diagnosed with normosmic hypogonadotropic hypogonadism/Kallmann Syndrome.
    Poch A; Dougherty MP; Roman RA; Chorich L; Hawkins Z; Kim SH; Kim HG; Layman LC
    Mol Cell Endocrinol; 2024 Aug; 589():112224. PubMed ID: 38593951
    [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. Molecular genetics of isolated hypogonadotropic hypogonadism and Kallmann syndrome.
    Karges B; Roux N
    Endocr Dev; 2005; 8():67-80. PubMed ID: 15722618
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. The genetics of hypogonadotropic hypogonadism.
    Bhagavath B; Layman LC
    Semin Reprod Med; 2007 Jul; 25(4):272-86. PubMed ID: 17594608
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Genetics of hypogonadotropic Hypogonadism-Human and mouse genes, inheritance, oligogenicity, and genetic counseling.
    Louden ED; Poch A; Kim HG; Ben-Mahmoud A; Kim SH; Layman LC
    Mol Cell Endocrinol; 2021 Aug; 534():111334. PubMed ID: 34062169
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 9.