These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 26629483)

  • 1. Study on KAL1 Gene Mutations in Idiopathic Hypogonadotropic Hypogonadism Patients with X-Linked Recessive Inheritance.
    Ahmadzadeh A; Ghods E; Mojarrad M; Aboutorabi R; Afkhamizadeh M; Bonakdaran S; Mosavi Z; Taghavi SM; Hassanzadeh Nazarabadi M
    Int J Mol Cell Med; 2015; 4(3):152-9. PubMed ID: 26629483
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Kallmann syndrome and ichthyosis: a case of contiguous gene deletion syndrome.
    Berges-Raso I; Giménez-Palop O; Gabau E; Capel I; Caixàs A; Rigla M
    Endocrinol Diabetes Metab Case Rep; 2017 Sep; 2017():. PubMed ID: 30352392
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Kallmann syndrome: Diagnostics and management.
    Kumar Yadav R; Qi B; Wen J; Gang X; Banerjee S
    Clin Chim Acta; 2025 Jan; 565():119994. PubMed ID: 39384129
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel fibroblast growth factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia.
    Trarbach EB; Costa EM; Versiani B; de Castro M; Baptista MT; Garmes HM; de Mendonca BB; Latronico AC
    J Clin Endocrinol Metab; 2006 Oct; 91(10):4006-12. PubMed ID: 16882753
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 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. Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism.
    Beranova M; Oliveira LM; Bédécarrats GY; Schipani E; Vallejo M; Ammini AC; Quintos JB; Hall JE; Martin KA; Hayes FJ; Pitteloud N; Kaiser UB; Crowley WF; Seminara SB
    J Clin Endocrinol Metab; 2001 Apr; 86(4):1580-8. PubMed ID: 11297587
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patients.
    Gu WJ; Zhang Q; Wang YQ; Yang GQ; Hong TP; Zhu DL; Yang JK; Ning G; Jin N; Chen K; Zang L; Wang AP; Du J; Wang XL; Yang LJ; Ba JM; Lv ZH; Dou JT; Mu YM
    Exp Biol Med (Maywood); 2015 Nov; 240(11):1480-9. PubMed ID: 26031747
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Parallel Multi-Gene Panel Testing for Diagnosis of Idiopathic Hypogonadotropic Hypogonadism/Kallmann Syndrome.
    Senthilraja M; Chapla A; Jebasingh FK; Naik D; Paul TV; Thomas N
    Case Rep Genet; 2019; 2019():4218514. PubMed ID: 31781422
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical characteristics and follow-up of 5 young Chinese males with gonadotropin-releasing hormone deficiency caused by mutations in the KAL1 gene.
    Li J; Li N; Ding Y; Huang X; Shen Y; Wang J; Wang X
    Meta Gene; 2016 Feb; 7():64-9. PubMed ID: 26862482
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Expanding the genetic spectrum of ANOS1 mutations in patients with congenital hypogonadotropic hypogonadism.
    Gonçalves CI; Fonseca F; Borges T; Cunha F; Lemos MC
    Hum Reprod; 2017 Mar; 32(3):704-711. PubMed ID: 28122887
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [GnRH deficiency: new insights from genetics].
    Kottler ML; Hamel A; Malville E; Richard N
    J Soc Biol; 2004; 198(1):80-7. PubMed ID: 15146960
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism.
    Bhagavath B; Podolsky RH; Ozata M; Bolu E; Bick DP; Kulharya A; Sherins RJ; Layman LC
    Fertil Steril; 2006 Mar; 85(3):706-13. PubMed ID: 16500342
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Genetic insights into human isolated gonadotropin deficiency.
    Trarbach EB; Silveira LG; Latronico AC
    Pituitary; 2007; 10(4):381-91. PubMed ID: 17624596
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mutation of the KAL1 gene in 30 male patients with idiopathic hypogonadotropic hypogonadism].
    Ma C; Jiang ZZ; Li XF; Yun X; Fu C; Liu RZ
    Zhonghua Nan Ke Xue; 2011 Jan; 17(1):32-7. PubMed ID: 21351529
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of three novel mutations in the KAL1 gene in patients with Kallmann syndrome.
    Söderlund D; Canto P; Méndez JP
    J Clin Endocrinol Metab; 2002 Jun; 87(6):2589-92. PubMed ID: 12050219
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of the KAL1 gene in 19 Japanese patients with Kallmann syndrome.
    Izumi Y; Tatsumi K; Okamoto S; Ogawa T; Hosokawa A; Matsuo T; Kato Y; Fukui H; Amino N
    Endocr J; 2001 Apr; 48(2):143-9. PubMed ID: 11456260
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism.
    Versiani BR; Trarbach E; Koenigkam-Santos M; Dos Santos AC; Elias LL; Moreira AC; Latronico AC; de Castro M
    Clin Endocrinol (Oxf); 2007 Feb; 66(2):173-9. PubMed ID: 17223984
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.