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Items: 1 to 20 of 85

1.

Childhood growth in boys with congenital hypogonadotropic hypogonadism.

Varimo T, Hero M, Laitinen EM, Miettinen PJ, Tommiska J, Känsäkoski J, Juul A, Raivio T.

Pediatr Res. 2016 May;79(5):705-9. doi: 10.1038/pr.2015.278. Epub 2015 Dec 31.

PMID:
26720605
2.

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. doi: 10.1016/j.ejmg.2014.04.002. Epub 2014 Apr 13.

PMID:
24732674
3.

Congenital hypogonadotropic hypogonadism in females: clinical spectrum, evaluation and genetics.

Bry-Gauillard H, Trabado S, Bouligand J, Sarfati J, Francou B, Salenave S, Chanson P, Brailly-Tabard S, Guiochon-Mantel A, Young J.

Ann Endocrinol (Paris). 2010 May;71(3):158-62. doi: 10.1016/j.ando.2010.02.024. Epub 2010 Apr 3. Review.

PMID:
20363464
4.

Isolated cryptorchidism: no evidence for involvement of genes underlying isolated hypogonadotropic hypogonadism.

Laitinen EM, Tommiska J, Virtanen HE, Oehlandt H, Koivu R, Vaaralahti K, Toppari J, Raivio T.

Mol Cell Endocrinol. 2011 Jul 20;341(1-2):35-8. doi: 10.1016/j.mce.2011.05.015. Epub 2011 Jun 1.

PMID:
21664240
5.

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 26;30(10):1111-1118. doi: 10.1515/jpem-2017-0035.

PMID:
28915117
6.

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. Epub 2007 Dec 26.

PMID:
18160472
7.
8.

Reversible congenital hypogonadotropic hypogonadism in patients with CHD7, FGFR1 or GNRHR mutations.

Laitinen EM, Tommiska J, Sane T, Vaaralahti K, Toppari J, Raivio T.

PLoS One. 2012;7(6):e39450. doi: 10.1371/journal.pone.0039450. Epub 2012 Jun 19.

9.

Hypogonadotropic hypogonadism.

Layman LC.

Endocrinol Metab Clin North Am. 2007 Jun;36(2):283-96. Review.

PMID:
17543719
10.

[GnRH deficiency: new insights from genetics].

Kottler ML, Hamel A, Malville E, Richard N.

J Soc Biol. 2004;198(1):80-7. Review. French.

PMID:
15146960
11.

[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. doi: 10.1016/S0003-4266(10)70005-6. French.

PMID:
21237329
12.

Variants in congenital hypogonadotrophic hypogonadism genes identified in an Indonesian cohort of 46,XY under-virilised boys.

Ayers KL, Bouty A, Robevska G, van den Bergen JA, Juniarto AZ, Listyasari NA, Sinclair AH, Faradz SM.

Hum Genomics. 2017 Feb 16;11(1):1. doi: 10.1186/s40246-017-0098-2.

13.

Triallelic digenic mutation in the prokineticin 2 and GNRH receptor genes in two brothers with normosmic congenital hypogonadotropic hypogonadism.

Méndez JP, Zenteno JC, Coronel A, Soriano-Ursúa MA, Valencia-Villalvazo EY, Soderlund D, Coral-Vázquez RM, Canto P.

Endocr Res. 2015;40(3):166-71. doi: 10.3109/07435800.2014.982327. Epub 2014 Dec 22.

PMID:
25531638
14.

The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism.

Bianco SD, Kaiser UB.

Nat Rev Endocrinol. 2009 Oct;5(10):569-76. doi: 10.1038/nrendo.2009.177. Epub 2009 Aug 25. Review.

15.

[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. Chinese.

PMID:
25619354
16.

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. doi: 10.1159/000152034. Epub 2008 Nov 5. Review.

17.

Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype-phenotype relationships.

Brioude F, Bouligand J, Trabado S, Francou B, Salenave S, Kamenicky P, Brailly-Tabard S, Chanson P, Guiochon-Mantel A, Young J.

Eur J Endocrinol. 2010 May;162(5):835-51. doi: 10.1530/EJE-10-0083. Epub 2010 Mar 5. Review.

PMID:
20207726
18.
19.

Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.

Canto P, Munguía P, Söderlund D, Castro JJ, Méndez JP.

J Androl. 2009 Jan-Feb;30(1):41-5. doi: 10.2164/jandrol.108.005314. Epub 2008 Aug 21.

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