178 related articles for article (PubMed ID: 20543690)
41. [Diagnosis of delayed puberty].
Busiah K; Belien V; Dallot N; Fila M; Guilbert J; Harroche A; Leger J
Arch Pediatr; 2007 Sep; 14(9):1101-10. PubMed ID: 17658248
[TBL] [Abstract][Full Text] [Related]
42. Review of human genetic and clinical studies directly relevant to GnRH signalling.
Seminara SB; Topaloglu AK
J Neuroendocrinol; 2022 May; 34(5):e13080. PubMed ID: 34970798
[TBL] [Abstract][Full Text] [Related]
43. 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]
44. Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism.
Topaloğlu AK
J Clin Res Pediatr Endocrinol; 2017 Dec; 9(Suppl 2):113-122. PubMed ID: 29280744
[TBL] [Abstract][Full Text] [Related]
45. Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel
Nalbantoğlu Ö; Arslan G; Köprülü Ö; Hazan F; Gürsoy S; Özkan B
J Clin Res Pediatr Endocrinol; 2019 Nov; 11(4):444-448. PubMed ID: 30905142
[TBL] [Abstract][Full Text] [Related]
46. Reversible isolated hypogonadotropic hypogonadism due to mutations in the neurokinin B regulation of gonadotropin-releasing hormone release.
Root AW
J Clin Endocrinol Metab; 2010 Jun; 95(6):2625-9. PubMed ID: 20525912
[No Abstract] [Full Text] [Related]
47. Genetics of isolated hypogonadotropic hypogonadism: role of GnRH receptor and other genes.
Beate K; Joseph N; Nicolas de R; Wolfram K
Int J Endocrinol; 2012; 2012():147893. PubMed ID: 22229029
[TBL] [Abstract][Full Text] [Related]
48. Use of genetic models of idiopathic hypogonadotrophic hypogonadism in mice and men to understand the mechanisms of disease.
Lippincott MF; True C; Seminara SB
Exp Physiol; 2013 Nov; 98(11):1522-7. PubMed ID: 23955308
[TBL] [Abstract][Full Text] [Related]
49. Delayed puberty due to a novel mutation in CHD7 causing CHARGE syndrome.
Dauber A; Hirschhorn JN; Picker J; Maher TA; Milunsky A
Pediatrics; 2010 Dec; 126(6):e1594-8. PubMed ID: 21041284
[TBL] [Abstract][Full Text] [Related]
50. Kallmann syndrome and idiopathic hypogonadotropic hypogonadism: The role of semaphorin signaling on GnRH neurons.
Cariboni A; Balasubramanian R
Handb Clin Neurol; 2021; 182():307-315. PubMed ID: 34266601
[TBL] [Abstract][Full Text] [Related]
51. Normosmic congenital hypogonadotropic hypogonadism due to TAC3/TACR3 mutations: characterization of neuroendocrine phenotypes and novel mutations.
Francou B; Bouligand J; Voican A; Amazit L; Trabado S; Fagart J; Meduri G; Brailly-Tabard S; Chanson P; Lecomte P; Guiochon-Mantel A; Young J
PLoS One; 2011; 6(10):e25614. PubMed ID: 22031817
[TBL] [Abstract][Full Text] [Related]
52. Recent advances in the understanding and management of delayed puberty.
Wei C; Crowne EC
Arch Dis Child; 2016 May; 101(5):481-8. PubMed ID: 26353794
[TBL] [Abstract][Full Text] [Related]
53. Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism.
Gürbüz F; Kotan LD; Mengen E; Şıklar Z; Berberoğlu M; Dökmetaş S; Kılıçlı MF; Güven A; Kirel B; Saka N; Poyrazoğlu Ş; Cesur Y; Doğan M; Özen S; Özbek MN; Demirbilek H; Kekil MB; Temiz F; Önenli Mungan N; Yüksel B; Topaloğlu AK
J Clin Res Pediatr Endocrinol; 2012 Sep; 4(3):121-6. PubMed ID: 22766261
[TBL] [Abstract][Full Text] [Related]
54. [The genetic control of puberty onset].
de Roux N; Villanueva C
Bull Acad Natl Med; 2012 Feb; 196(2):327-40; discussion 340-3. PubMed ID: 23420953
[TBL] [Abstract][Full Text] [Related]
55. The mystery of puberty initiation: genetics and epigenetics of idiopathic central precocious puberty (ICPP).
Leka-Emiri S; Chrousos GP; Kanaka-Gantenbein C
J Endocrinol Invest; 2017 Aug; 40(8):789-802. PubMed ID: 28251550
[TBL] [Abstract][Full Text] [Related]
56. Biology of kisspeptins.
Hameed S; Dhillo WS
Front Horm Res; 2010; 39():25-36. PubMed ID: 20389083
[TBL] [Abstract][Full Text] [Related]
57. TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients.
Noel SD; Abreu AP; Xu S; Muyide T; Gianetti E; Tusset C; Carroll J; Latronico AC; Seminara SB; Carroll RS; Kaiser UB
FASEB J; 2014 Apr; 28(4):1924-37. PubMed ID: 24376026
[TBL] [Abstract][Full Text] [Related]
58. Constitutional delay of puberty versus congenital hypogonadotropic hypogonadism: Genetics, management and updates.
Raivio T; Miettinen PJ
Best Pract Res Clin Endocrinol Metab; 2019 Jun; 33(3):101316. PubMed ID: 31522908
[TBL] [Abstract][Full Text] [Related]
59. Delayed Puberty-Phenotypic Diversity, Molecular Genetic Mechanisms, and Recent Discoveries.
Howard SR; Dunkel L
Endocr Rev; 2019 Oct; 40(5):1285-1317. PubMed ID: 31220230
[TBL] [Abstract][Full Text] [Related]
60. Molecular evaluation of the gonadotropin-releasing hormone receptor.
Cohen DP
Semin Reprod Med; 2000; 18(1):11-6. PubMed ID: 11299515
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
