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Journal Abstract Search

471 related items for PubMed ID: 18985070

  • 1. Kallmann syndrome.
    Dodé C, Hardelin JP.
    Eur J Hum Genet; 2009 Feb; 17(2):139-46. PubMed ID: 18985070
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  • 3. The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.
    Hardelin JP, Dodé C.
    Sex Dev; 2008 Feb; 2(4-5):181-93. PubMed ID: 18987492
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  • 8. Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome.
    Leroy C, Fouveaut C, Leclercq S, Jacquemont S, Boullay HD, Lespinasse J, Delpech M, Dupont JM, Hardelin JP, Dodé C.
    Eur J Hum Genet; 2008 Jul; 16(7):865-8. PubMed ID: 18285834
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  • 10. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.
    Abreu AP, Trarbach EB, de Castro M, Frade Costa EM, Versiani B, Matias Baptista MT, Garmes HM, Mendonca BB, Latronico AC.
    J Clin Endocrinol Metab; 2008 Oct; 93(10):4113-8. PubMed ID: 18682503
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  • 15. 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
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  • 17. Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.
    Dodé C, Teixeira L, Levilliers J, Fouveaut C, Bouchard P, Kottler ML, Lespinasse J, Lienhardt-Roussie A, Mathieu M, Moerman A, Morgan G, Murat A, Toublanc JE, Wolczynski S, Delpech M, Petit C, Young J, Hardelin JP.
    PLoS Genet; 2006 Oct 20; 2(10):e175. PubMed ID: 17054399
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  • 20. 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 20; 98(5):E943-53. PubMed ID: 23533228
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