178 related articles for article (PubMed ID: 15004876)
1. Mutation analysis of the KAL gene in female patients with gonadotropin-releasing hormone deficiency.
Lee SH; Han JH; Cho SW; Lee WH; Cha KY; Lee MH
Yonsei Med J; 2004 Feb; 45(1):107-12. PubMed ID: 15004876
[TBL] [Abstract][Full Text] [Related]
2. A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome.
Maya-Nuñez G; Zenteno JC; Ulloa-Aguirre A; Kofman-Alfaro S; Mendez JP
J Clin Endocrinol Metab; 1998 May; 83(5):1650-3. PubMed ID: 9589672
[TBL] [Abstract][Full Text] [Related]
3. The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.
Oliveira LM; Seminara SB; Beranova M; Hayes FJ; Valkenburgh SB; Schipani E; Costa EM; Latronico AC; Crowley WF; Vallejo M
J Clin Endocrinol Metab; 2001 Apr; 86(4):1532-8. PubMed ID: 11297579
[TBL] [Abstract][Full Text] [Related]
4. Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization.
Quinton R; Duke VM; Robertson A; Kirk JM; Matfin G; de Zoysa PA; Azcona C; MacColl GS; Jacobs HS; Conway GS; Besser M; Stanhope RG; Bouloux PM
Clin Endocrinol (Oxf); 2001 Aug; 55(2):163-74. PubMed ID: 11531922
[TBL] [Abstract][Full Text] [Related]
5. The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human.
Waldstreicher J; Seminara SB; Jameson JL; Geyer A; Nachtigall LB; Boepple PA; Holmes LB; Crowley WF
J Clin Endocrinol Metab; 1996 Dec; 81(12):4388-95. PubMed ID: 8954047
[TBL] [Abstract][Full Text] [Related]
6. [GnRH deficiency: new insights from genetics].
Kottler ML; Hamel A; Malville E; Richard N
J Soc Biol; 2004; 198(1):80-7. PubMed ID: 15146960
[TBL] [Abstract][Full Text] [Related]
7. Genetic heterogeneity evidenced by low incidence of KAL-1 gene mutations in sporadic cases of gonadotropin-releasing hormone deficiency.
Georgopoulos NA; Pralong FP; Seidman CE; Seidman JG; Crowley WF; Vallejo M
J Clin Endocrinol Metab; 1997 Jan; 82(1):213-7. PubMed ID: 8989261
[TBL] [Abstract][Full Text] [Related]
8. Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patients.
Trarbach EB; Baptista MT; Garmes HM; Hackel C
J Endocrinol; 2005 Dec; 187(3):361-8. PubMed ID: 16423815
[TBL] [Abstract][Full Text] [Related]
9. A novel nonsense mutation of the KAL gene in two brothers with Kallmann syndrome.
Jansen C; Hendriks-Stegeman BI; Jansen M
Horm Res; 2000; 53(4):207-12. PubMed ID: 11044805
[TBL] [Abstract][Full Text] [Related]
10. X-linked GnRH deficiency: role of KAL-1 mutations in GnRH deficiency.
Hu Y; Bouloux PM
Mol Cell Endocrinol; 2011 Oct; 346(1-2):13-20. PubMed ID: 21497178
[TBL] [Abstract][Full Text] [Related]
11. The genetics of hypogonadotropic hypogonadism.
Bhagavath B; Layman LC
Semin Reprod Med; 2007 Jul; 25(4):272-86. PubMed ID: 17594608
[TBL] [Abstract][Full Text] [Related]
12. The product of X-linked Kallmann's syndrome gene (KAL1) affects the migratory activity of gonadotropin-releasing hormone (GnRH)-producing neurons.
Cariboni A; Pimpinelli F; Colamarino S; Zaninetti R; Piccolella M; Rumio C; Piva F; Rugarli EI; Maggi R
Hum Mol Genet; 2004 Nov; 13(22):2781-91. PubMed ID: 15471890
[TBL] [Abstract][Full Text] [Related]
13. [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. PubMed ID: 25619354
[TBL] [Abstract][Full Text] [Related]
14. 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
J Clin Endocrinol Metab; 2006 Oct; 91(10):4006-12. PubMed ID: 16882753
[TBL] [Abstract][Full Text] [Related]
15. Molecular analysis of KAL-1 in a series of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism patients from Northwestern China.
Tang KF; Wu QF; Zou TJ; Xue W; Wang XY; Xing JP
Asian J Androl; 2009 Nov; 11(6):711-5. PubMed ID: 19734936
[TBL] [Abstract][Full Text] [Related]
16. Physiologic and genetic insights into the pathophysiology and management of hypogonadotropic hypogonadism.
Hall JE
Ann Endocrinol (Paris); 1999 Jul; 60(2):93-101. PubMed ID: 10456179
[TBL] [Abstract][Full Text] [Related]
17. X chromosome-linked Kallmann syndrome: clinical heterogeneity in three siblings carrying an intragenic deletion of the KAL-1 gene.
Massin N; Pêcheux C; Eloit C; Bensimon JL; Galey J; Kuttenn F; Hardelin JP; Dodé C; Touraine P
J Clin Endocrinol Metab; 2003 May; 88(5):2003-8. PubMed ID: 12727945
[TBL] [Abstract][Full Text] [Related]
18. KAL1 mutations are not a common cause of idiopathic hypogonadotrophic hypogonadism in humans.
Bhagavath B; Xu N; Ozata M; Rosenfield RL; Bick DP; Sherins RJ; Layman LC
Mol Hum Reprod; 2007 Mar; 13(3):165-70. PubMed ID: 17213338
[TBL] [Abstract][Full Text] [Related]
19. Familial Kallmann syndrome: a novel splice acceptor mutation in the KAL gene.
O'Neill MJ; Tridjaja B; Smith MJ; Bell KM; Warne GL; Sinclair AH
Hum Mutat; 1998; 11(4):340-2. PubMed ID: 9554756
[TBL] [Abstract][Full Text] [Related]
20. 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; Dwyer AA; Plummer L; Fliers E; Boepple P; Hayes F; Seminara S; Hughes VA; Ma J; Bouloux P; Mohammadi M; Crowley WF
Mol Cell Endocrinol; 2006 Jul; 254-255():60-9. PubMed ID: 16764984
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
