Similar articles for PMID: 15001591

Year	Number of Results
1975	1
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1997	1
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2024	1

1

Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

Sato N, Katsumata N, Kagami M, Hasegawa T, Hori N, Kawakita S, Minowada S, Shimotsuka A, Shishiba Y, Yokozawa M, Yasuda T, Nagasaki K, Hasegawa D, Hasegawa Y, Tachibana K, Naiki Y, Horikawa R, Tanaka T, Ogata T. Sato N, et al. J Clin Endocrinol Metab. 2004 Mar;89(3):1079-88. doi: 10.1210/jc.2003-030476. J Clin Endocrinol Metab. 2004. PMID: 15001591

2

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. Trarbach EB, et al. J Clin Endocrinol Metab. 2006 Oct;91(10):4006-12. doi: 10.1210/jc.2005-2793. Epub 2006 Aug 1. J Clin Endocrinol Metab. 2006. PMID: 16882753

3

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. Versiani BR, et al. Clin Endocrinol (Oxf). 2007 Feb;66(2):173-9. doi: 10.1111/j.1365-2265.2006.02702.x. Clin Endocrinol (Oxf). 2007. PMID: 17223984

4

[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. Qin M, et al. Zhonghua Er Ke Za Zhi. 2014 Dec;52(12):942-7. Zhonghua Er Ke Za Zhi. 2014. PMID: 25619354 Chinese.

5

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. Salenave S, et al. J Clin Endocrinol Metab. 2008 Mar;93(3):758-63. doi: 10.1210/jc.2007-1168. Epub 2007 Dec 26. J Clin Endocrinol Metab. 2008. PMID: 18160472

6

Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2).

Albuisson J, Pêcheux C, Carel JC, Lacombe D, Leheup B, Lapuzina P, Bouchard P, Legius E, Matthijs G, Wasniewska M, Delpech M, Young J, Hardelin JP, Dodé C. Albuisson J, et al. Hum Mutat. 2005 Jan;25(1):98-9. doi: 10.1002/humu.9298. Hum Mutat. 2005. PMID: 15605412

7

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

Dodé C, Levilliers J, Dupont JM, De Paepe A, Le Dû N, Soussi-Yanicostas N, Coimbra RS, Delmaghani S, Compain-Nouaille S, Baverel F, Pêcheux C, Le Tessier D, Cruaud C, Delpech M, Speleman F, Vermeulen S, Amalfitano A, Bachelot Y, Bouchard P, Cabrol S, Carel JC, Delemarre-van de Waal H, Goulet-Salmon B, Kottler ML, Richard O, Sanchez-Franco F, Saura R, Young J, Petit C, Hardelin JP. Dodé C, et al. Nat Genet. 2003 Apr;33(4):463-5. doi: 10.1038/ng1122. Epub 2003 Mar 10. Nat Genet. 2003. PMID: 12627230

8

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. Gu WJ, et al. Exp Biol Med (Maywood). 2015 Nov;240(11):1480-9. doi: 10.1177/1535370215587531. Epub 2015 Jun 1. Exp Biol Med (Maywood). 2015. PMID: 26031747 Free PMC article.

9

Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.

Pitteloud N, Meysing A, Quinton R, Acierno JS Jr, Dwyer AA, Plummer L, Fliers E, Boepple P, Hayes F, Seminara S, Hughes VA, Ma J, Bouloux P, Mohammadi M, Crowley WF Jr. Pitteloud N, et al. Mol Cell Endocrinol. 2006 Jul 25;254-255:60-9. doi: 10.1016/j.mce.2006.04.021. Epub 2006 Jun 9. Mol Cell Endocrinol. 2006. PMID: 16764984

10

[GnRH deficiency: new insights from genetics].

Kottler ML, Hamel A, Malville E, Richard N. Kottler ML, et al. J Soc Biol. 2004;198(1):80-7. J Soc Biol. 2004. PMID: 15146960 Review. French.

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