307 related articles for article (PubMed ID: 17543719)
21. Clinical manifestations of impaired GnRH neuron development and function.
Kim HG; Bhagavath B; Layman LC
Neurosignals; 2008; 16(2-3):165-82. PubMed ID: 18253056
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. [Normosmic idiopathic hypogonadotropic hypogonadism with GnRH receptor mutation(review)].
Tamaya T
Nihon Rinsho; 2002 Feb; 60(2):319-24. PubMed ID: 11857920
[TBL] [Abstract][Full Text] [Related]
24. The role of gene defects underlying isolated hypogonadotropic hypogonadism in patients with constitutional delay of growth and puberty.
Vaaralahti K; Wehkalampi K; Tommiska J; Laitinen EM; Dunkel L; Raivio T
Fertil Steril; 2011 Jun; 95(8):2756-8. PubMed ID: 21292259
[TBL] [Abstract][Full Text] [Related]
25. Long-term outcome of idiopathic hypogonadotropic hypogonadism.
King TF; Hayes FJ
Curr Opin Endocrinol Diabetes Obes; 2012 Jun; 19(3):204-10. PubMed ID: 22499222
[TBL] [Abstract][Full Text] [Related]
26. 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
Hum Mutat; 2005 Jan; 25(1):98-9. PubMed ID: 15605412
[TBL] [Abstract][Full Text] [Related]
27. [Isolated gonadotropin deficiency].
Takakura K
Nihon Rinsho; 2006 May; Suppl 1():63-6. PubMed ID: 16776094
[No Abstract] [Full Text] [Related]
28. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1.
Trarbach EB; Teles MG; Costa EM; Abreu AP; Garmes HM; Guerra G; Baptista MT; de Castro M; Mendonca BB; Latronico AC
Clin Endocrinol (Oxf); 2010 Mar; 72(3):371-6. PubMed ID: 19489874
[TBL] [Abstract][Full Text] [Related]
29. [Molecular genetics of Kallmann syndrome: an update].
Fu C; Feng Z; Liu RZ
Zhonghua Nan Ke Xue; 2011 Apr; 17(4):361-5. PubMed ID: 21548217
[TBL] [Abstract][Full Text] [Related]
30. 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. PubMed ID: 18160472
[TBL] [Abstract][Full Text] [Related]
31. Molecular causes of hypogonadotropic hypogonadism.
Topaloglu AK; Kotan LD
Curr Opin Obstet Gynecol; 2010 Aug; 22(4):264-70. PubMed ID: 20543690
[TBL] [Abstract][Full Text] [Related]
32. Pathogenesis and management of abnormal puberty.
Hopwood NJ
Spec Top Endocrinol Metab; 1985; 7():175-236. PubMed ID: 3914096
[TBL] [Abstract][Full Text] [Related]
33. [The status of the gonadotropin releasing hormone test in differential diagnosis of delayed puberty in adolescents over 14 years of age].
Jungmann E; Trautermann C
Med Klin (Munich); 1994 Oct; 89(10):529-33. PubMed ID: 7808353
[TBL] [Abstract][Full Text] [Related]
34. GnRH receptor mutations in isolated gonadotropic deficiency.
Chevrier L; Guimiot F; de Roux N
Mol Cell Endocrinol; 2011 Oct; 346(1-2):21-8. PubMed ID: 21645587
[TBL] [Abstract][Full Text] [Related]
35. A genetic basis for functional hypothalamic amenorrhea.
Caronia LM; Martin C; Welt CK; Sykiotis GP; Quinton R; Thambundit A; Avbelj M; Dhruvakumar S; Plummer L; Hughes VA; Seminara SB; Boepple PA; Sidis Y; Crowley WF; Martin KA; Hall JE; Pitteloud N
N Engl J Med; 2011 Jan; 364(3):215-25. PubMed ID: 21247312
[TBL] [Abstract][Full Text] [Related]
36. Role of sequence variations of the GnRH receptor and G protein-coupled receptor 54 gene in male idiopathic hypogonadotropic hypogonadism.
Lanfranco F; Gromoll J; von Eckardstein S; Herding EM; Nieschlag E; Simoni M
Eur J Endocrinol; 2005 Dec; 153(6):845-52. PubMed ID: 16322390
[TBL] [Abstract][Full Text] [Related]
37. Loss of function mutations of the GnRH receptor: a new cause of hypogonadotropic hypogonadism.
de Roux N; Young J; Misrahi M; Schaison G; Milgrom E
J Pediatr Endocrinol Metab; 1999 Apr; 12 Suppl 1():267-75. PubMed ID: 10698591
[TBL] [Abstract][Full Text] [Related]
38. The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
Semple RK; Topaloglu AK
Clin Endocrinol (Oxf); 2010 Apr; 72(4):427-35. PubMed ID: 19719764
[TBL] [Abstract][Full Text] [Related]
39. [Diagnosis and treatment of hypogonadotropism in males and females].
Young J; Schaison G
Rev Prat; 1999 Jun; 49(12):1283-9. PubMed ID: 10488659
[TBL] [Abstract][Full Text] [Related]
40. The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism.
Bianco SD; Kaiser UB
Nat Rev Endocrinol; 2009 Oct; 5(10):569-76. PubMed ID: 19707180
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
