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Items: 1 to 20 of 70

1.

Genetics of male hypogonadotropic hypogonadism.

Sato N.

Pediatr Endocrinol Rev. 2012 Oct;10 Suppl 1:110-25. Review. No abstract available.

PMID:
23330252
2.

Kallmann's syndrome and normosmic isolated hypogonadotropic hypogonadism: two largely overlapping manifestations of one rare disorder.

Network for Central Hypogonadism (Network Ipogonadismo Centrale, NICe) of Italian Societies of Endocrinology (SIE), of Andrology and Sexual Medicine (SIAMS) and of Peadiatric Endocrinology and Diabetes (SIEDP).

J Endocrinol Invest. 2014 May;37(5):499-500. doi: 10.1007/s40618-014-0063-z. Epub 2014 Apr 9. No abstract available.

3.

[Idiopathic hypogonadotropic hypogonadism according to Mendel].

Epelbaum J.

Med Sci (Paris). 2007 May;23(5):485. French. No abstract available.

PMID:
17502064
4.

Diagnosis and evaluation of hypogonadism.

McCabe MJ, Bancalari RE, Dattani MT.

Pediatr Endocrinol Rev. 2014 Feb;11 Suppl 2:214-29. Review.

PMID:
24683946
5.

Genetic insights into human isolated gonadotropin deficiency.

Trarbach EB, Silveira LG, Latronico AC.

Pituitary. 2007;10(4):381-91. Review.

PMID:
17624596
6.

[The genetics of hypogonadotropic hypogonadism in the male].

Sievers C, Schneider HJ, Stalla GK.

MMW Fortschr Med. 2005 Nov 10;147(45):32-4, 36. Review. German.

PMID:
16320650
7.

Hypogonadotropic hypogonadism: gonadotropin-releasing hormone therapy.

Whitcomb RW, Crowley WF Jr.

Curr Ther Endocrinol Metab. 1994;5:303-5. No abstract available.

PMID:
7704740
8.

The genetics of hypogonadotropic hypogonadism.

Bhagavath B, Layman LC.

Semin Reprod Med. 2007 Jul;25(4):272-86. Review.

PMID:
17594608
9.

Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory.

Mitchell AL, Dwyer A, Pitteloud N, Quinton R.

Trends Endocrinol Metab. 2011 Jul;22(7):249-58. doi: 10.1016/j.tem.2011.03.002. Epub 2011 Apr 20.

PMID:
21511493
10.

Hypogonadotropic hypogonadism in women.

Skałba P, Guz M.

Endokrynol Pol. 2011;62(6):560-7.

11.

[Therapeutic importance of the diagnosis of Kallmann syndrome].

Gasztonyi Z, Paulin F, Siklósi G, Czeizel E.

Orv Hetil. 1997 Oct 5;138(40):2529-32. Hungarian.

PMID:
9411323
13.

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.

PMID:
16500342
14.

Female hypogonadotropic hypogonadism. Hypothalamic amenorrhea syndrome.

Yen SS.

Endocrinol Metab Clin North Am. 1993 Mar;22(1):29-58. Review.

PMID:
8449187
15.

[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
16.

Clinical manifestations of impaired GnRH neuron development and function.

Kim HG, Bhagavath B, Layman LC.

Neurosignals. 2008;16(2-3):165-82. doi: 10.1159/000111561. Epub 2008 Feb 5. Review.

PMID:
18253056
17.

A review of Kallmann syndrome: genetics, pathophysiology, and clinical management.

Fechner A, Fong S, McGovern P.

Obstet Gynecol Surv. 2008 Mar;63(3):189-94. doi: 10.1097/OGX.0b013e3181641278. Review.

PMID:
18279545
18.

[The Kallmann syndrome. Its pathophysiology and clinical picture].

Meschede D, Behre HM, Nieschlag E, Horst J.

Dtsch Med Wochenschr. 1994 Oct 21;119(42):1436-42. Review. German. No abstract available.

PMID:
7956761
19.

Circulating antimüllerian hormone levels in boys decline during early puberty and correlate with inhibin B.

Hero M, Tommiska J, Vaaralahti K, Laitinen EM, Sipilä I, Puhakka L, Dunkel L, Raivio T.

Fertil Steril. 2012 May;97(5):1242-7. doi: 10.1016/j.fertnstert.2012.02.020. Epub 2012 Mar 9.

PMID:
22405597
20.

[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. Chinese.

PMID:
21351529

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