174 related articles for article (PubMed ID: 33453020)
21. Olfactory phenotypic spectrum in idiopathic hypogonadotropic hypogonadism: pathophysiological and genetic implications.
Lewkowitz-Shpuntoff HM; Hughes VA; Plummer L; Au MG; Doty RL; Seminara SB; Chan YM; Pitteloud N; Crowley WF; Balasubramanian R
J Clin Endocrinol Metab; 2012 Jan; 97(1):E136-44. PubMed ID: 22072740
[TBL] [Abstract][Full Text] [Related]
22. A novel splice site variant in ANOS1 gene leads to Kallmann syndrome in three siblings.
Jiang X; Li D; Gao Y; Zhang X; Wang X; Yang Y; Shen Y
Gene; 2020 Feb; 726():144177. PubMed ID: 31669640
[TBL] [Abstract][Full Text] [Related]
23. Whole-Exome Sequencing Analysis of Idiopathic Hypogonadotropic Hypogonadism: Comparison of Varicocele and Nonobstructive Azoospermia.
Ma Z; Dai Y; Jin L; Luo Y; Guo C; Qu R; He S; Liu Y; Xia Y; Liu H; Kong L; Xu M; Zhang L; Zhao Y; Suliya Y; Yuan D; Yang L
Reprod Sci; 2024 Jan; 31(1):222-238. PubMed ID: 37679557
[TBL] [Abstract][Full Text] [Related]
24. Gonadal function and response to human chorionic and menopausal gonadotrophin therapy in male patients with idiopathic hypogonadotrophic hypogonadism.
Kirk JM; Savage MO; Grant DB; Bouloux PM; Besser GM
Clin Endocrinol (Oxf); 1994 Jul; 41(1):57-63. PubMed ID: 7914153
[TBL] [Abstract][Full Text] [Related]
25. The p190 RhoGAPs, ARHGAP35, and ARHGAP5 are implicated in GnRH neuronal development: Evidence from patients with idiopathic hypogonadotropic hypogonadism, zebrafish, and in vitro GAP activity assay.
Lippincott MF; Xu W; Smith AA; Miao X; Lafont A; Shennib O; Farley GJ; Sabbagh R; Delaney A; Stamou M; Plummer L; Salnikov K; Georgopoulos NA; Mericq V; Quinton R; Mau-Them FT; Nambot S; Hamad A; Brittain H; Tooze RS; Calpena E; Wilkie AOM; Willems M; Crowley WF; Balasubramanian R; Lamarche-Vane N; Davis EE; Seminara SB
Genet Med; 2022 Dec; 24(12):2501-2515. PubMed ID: 36178483
[TBL] [Abstract][Full Text] [Related]
26. [Diagnosis and treatment of idiopathic hypogonadotropic hypogonadism in males].
Yang L; Chen HS; Qu R; Zhang SX
Zhonghua Nan Ke Xue; 2018 Aug; 24(8):744-747. PubMed ID: 30173437
[TBL] [Abstract][Full Text] [Related]
27. A case report of congenital idiopathic hypogonadotropic hypogonadism caused by novel mutation of GNRHR gene.
Wang L; Lin W; Li X; Zhang L; Wang K; Cui X; Tang S; Fang G; Tan Y; Wang X; Chen C; Yang C; Tang H
Medicine (Baltimore); 2021 Feb; 100(5):e24007. PubMed ID: 33592857
[TBL] [Abstract][Full Text] [Related]
28. Molecular defects of the GnRH-receptor gene in Chinese patients with idiopathic hypogonadotropic hypogonadism and the severity of hypogonadism.
Fathi AK; Hu S; Fu X; Huang S; Liang Y; Ning Q; Luo X
J Pediatr Endocrinol Metab; 2012; 25(7-8):659-68. PubMed ID: 23155690
[TBL] [Abstract][Full Text] [Related]
29. [Target gene panel method versus whole-exome sequencing in detection of idiopathic hypogonadotropic hypogonadism in males].
Guo YJ; Guo YM; Han Y; Wu QY; Yang Y; Luo T; Xu XF; Xia XY
Zhonghua Nan Ke Xue; 2021 Oct; 27(10):899-903. PubMed ID: 34914268
[TBL] [Abstract][Full Text] [Related]
30. Exaggerated free alpha-subunit levels during pulsatile gonadotropin-releasing hormone replacement in women with idiopathic hypogonadotropic hypogonadism.
Lavoie HB; Martin KA; Taylor E; Crowley WF; Hall JE
J Clin Endocrinol Metab; 1998 Jan; 83(1):241-7. PubMed ID: 9435449
[TBL] [Abstract][Full Text] [Related]
31. Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism.
Moalla M; Hadj Kacem F; Al-Mutery AF; Mahfood M; Mejdoub-Rekik N; Abid M; Mnif-Feki M; Hadj Kacem H
J Assist Reprod Genet; 2019 Jun; 36(6):1273-1280. PubMed ID: 31073722
[TBL] [Abstract][Full Text] [Related]
32. Autosomal recessive idiopathic hypogonadotropic hypogonadism: genetic analysis excludes mutations in the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes.
Bo-Abbas Y; Acierno JS; Shagoury JK; Crowley WF; Seminara SB
J Clin Endocrinol Metab; 2003 Jun; 88(6):2730-7. PubMed ID: 12788881
[TBL] [Abstract][Full Text] [Related]
33. Congenital idiopathic hypogonadotropic hypogonadism: evidence of defects in the hypothalamus, pituitary, and testes.
Sykiotis GP; Hoang XH; Avbelj M; Hayes FJ; Thambundit A; Dwyer A; Au M; Plummer L; Crowley WF; Pitteloud N
J Clin Endocrinol Metab; 2010 Jun; 95(6):3019-27. PubMed ID: 20382682
[TBL] [Abstract][Full Text] [Related]
34. A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitalia.
Breuer O; Abdulhadi-Atwan M; Zeligson S; Fridman H; Renbaum P; Levy-Lahad E; Zangen DH
Eur J Endocrinol; 2012 Aug; 167(2):209-16. PubMed ID: 22619348
[TBL] [Abstract][Full Text] [Related]
35. The role of prior pubertal development, biochemical markers of testicular maturation, and genetics in elucidating the phenotypic heterogeneity of idiopathic hypogonadotropic hypogonadism.
Pitteloud N; Hayes FJ; Boepple PA; DeCruz S; Seminara SB; MacLaughlin DT; Crowley WF
J Clin Endocrinol Metab; 2002 Jan; 87(1):152-60. PubMed ID: 11788640
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese Cohort.
Li JD; Wu J; Zhao Y; Wang X; Jiang F; Hou Q; Chen DN; Zheng R; Yu R; Zhou W; Men M
J Clin Endocrinol Metab; 2020 May; 105(5):. PubMed ID: 31689711
[TBL] [Abstract][Full Text] [Related]
38. Responsiveness to a physiological regimen of GnRH therapy and relation to genotype in women with isolated hypogonadotropic hypogonadism.
Abel BS; Shaw ND; Brown JM; Adams JM; Alati T; Martin KA; Pitteloud N; Seminara SB; Plummer L; Pignatelli D; Crowley WF; Welt CK; Hall JE
J Clin Endocrinol Metab; 2013 Feb; 98(2):E206-16. PubMed ID: 23341491
[TBL] [Abstract][Full Text] [Related]
39. Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH).
Miura K; Acierno JS; Seminara SB
J Hum Genet; 2004; 49(5):265-8. PubMed ID: 15362570
[TBL] [Abstract][Full Text] [Related]
40. Complex genetics in idiopathic hypogonadotropic hypogonadism.
Pitteloud N; Durrani S; Raivio T; Sykiotis GP
Front Horm Res; 2010; 39():142-153. PubMed ID: 20389092
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]