BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 23650337)

  • 1. Clinical genetic testing for Kallmann syndrome.
    Layman LC
    J Clin Endocrinol Metab; 2013 May; 98(5):1860-2. PubMed ID: 23650337
    [No Abstract]   [Full Text] [Related]  

  • 2. Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes.
    Costa-Barbosa FA; Balasubramanian R; Keefe KW; Shaw ND; Al-Tassan N; Plummer L; Dwyer AA; Buck CL; Choi JH; Seminara SB; Quinton R; Monies D; Meyer B; Hall JE; Pitteloud N; Crowley WF
    J Clin Endocrinol Metab; 2013 May; 98(5):E943-53. PubMed ID: 23533228
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Kallmann syndrome in women: from genes to diagnosis and treatment.
    Meczekalski B; Podfigurna-Stopa A; Smolarczyk R; Katulski K; Genazzani AR
    Gynecol Endocrinol; 2013 Apr; 29(4):296-300. PubMed ID: 23368665
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Complex genetics in idiopathic hypogonadotropic hypogonadism.
    Pitteloud N; Durrani S; Raivio T; Sykiotis GP
    Front Horm Res; 2010; 39():142-153. PubMed ID: 20389092
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Kallmann syndrome].
    Fujieda K; Mukai T
    Nihon Rinsho; 2006 Apr; 64 Suppl 4():47-53. PubMed ID: 16689283
    [No Abstract]   [Full Text] [Related]  

  • 6. [Advances in the studies of Kallmann syndrome].
    Hao LJ; Cui YX
    Zhonghua Nan Ke Xue; 2006 Jul; 12(7):647-9. PubMed ID: 16894948
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Next-generation sequencing of patients with congenital anosmia.
    Alkelai A; Olender T; Dode C; Shushan S; Tatarskyy P; Furman-Haran E; Boyko V; Gross-Isseroff R; Halvorsen M; Greenbaum L; Milgrom R; Yamada K; Haneishi A; Blau I; Lancet D
    Eur J Hum Genet; 2017 Dec; 25(12):1377-1387. PubMed ID: 29255181
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Kallmann syndrome].
    Sato N; Ogata T
    Nihon Rinsho; 2006 Jun; Suppl 2():220-4. PubMed ID: 16817388
    [No Abstract]   [Full Text] [Related]  

  • 9. Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life.
    Sarfati J; Bouvattier C; Bry-Gauillard H; Cartes A; Bouligand J; Young J
    Orphanet J Rare Dis; 2015 Jun; 10():71. PubMed ID: 26051373
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Hypogonadotropic hypogonadism: new aspects in the regulation of hypothalamic-pituitary-gonadal axis].
    Brioude F; Bouvattier CE; Lombès M
    Ann Endocrinol (Paris); 2010 Sep; 71 Suppl 1():S33-41. PubMed ID: 21237329
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism.
    Aoyama K; Mizuno H; Tanaka T; Togawa T; Negishi Y; Ohashi K; Hori I; Izawa M; Hamajima T; Saitoh S
    J Pediatr Endocrinol Metab; 2017 Oct; 30(10):1111-1118. PubMed ID: 28915117
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical genetics of Kallmann syndrome.
    Dodé C; Hardelin JP
    Ann Endocrinol (Paris); 2010 May; 71(3):149-57. PubMed ID: 20362962
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Isolated hypogonadotropic hypogonadism].
    Shozu M
    Nihon Rinsho; 2006 Apr; 64 Suppl 4():202-6. PubMed ID: 16689309
    [No Abstract]   [Full Text] [Related]  

  • 14. Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients.
    Sarfati J; Fouveaut C; Leroy C; Jeanpierre M; Hardelin JP; Dodé C
    Eur J Endocrinol; 2013 Dec; 169(6):805-9. PubMed ID: 24031091
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.
    Hardelin JP; Dodé C
    Sex Dev; 2008; 2(4-5):181-93. PubMed ID: 18987492
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [Molecular genetics of Kallmann syndrome: an update].
    Fu C; Feng Z; Liu RZ
    Zhonghua Nan Ke Xue; 2011 Apr; 17(4):361-5. PubMed ID: 21548217
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mechanisms of disease: Insights into X-linked and autosomal-dominant Kallmann syndrome.
    Tsai PS; Gill JC
    Nat Clin Pract Endocrinol Metab; 2006 Mar; 2(3):160-71. PubMed ID: 16932275
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia.
    Raivio T; Avbelj M; McCabe MJ; Romero CJ; Dwyer AA; Tommiska J; Sykiotis GP; Gregory LC; Diaczok D; Tziaferi V; Elting MW; Padidela R; Plummer L; Martin C; Feng B; Zhang C; Zhou QY; Chen H; Mohammadi M; Quinton R; Sidis Y; Radovick S; Dattani MT; Pitteloud N
    J Clin Endocrinol Metab; 2012 Apr; 97(4):E694-9. PubMed ID: 22319038
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetics of congenital hypogonadotropic hypogonadism in Denmark.
    Tommiska J; Känsäkoski J; Christiansen P; Jørgensen N; Lawaetz JG; Juul A; Raivio T
    Eur J Med Genet; 2014 Jul; 57(7):345-8. PubMed ID: 24732674
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.