Tham khảo Chất đối kháng hormone giải phóng gonadotropin

  1. 1 2 Van Poppel H, Nilsson S (June 2008). Testosterone surge: rationale for gonadotropin-releasing hormone blockers? Urology 71: 1001-1006.
  2. ↑ Anderson J (May 2009). Degarelix: a novel gonadotropin-releasing hormone blocker for the treatment of prostate cancer. Future Oncol. 5: 433-443.
  3. ↑ Bodri D, Vernaeve V, Guillen JJ, et al (September 2006). Comparison between a GnRH antagonist and a GnRH agonist flare-up protocol in oocyte donors: a randomized clinical trial. Hum. Reprod. 21: 2246-2251.
  4. ↑ Lambalk CB, Leader A, Olivennes F, et al (March 2006). Treatment with the GnRH antagonist ganirelix prevents premature LH rises and luteinization in stimulated intrauterine insemination: results of a double-blind, placebo-controlled, multicentre trial. Hum. Reprod. 21: 632-639.
  5. ↑ Lee TH, Lin YH, Seow KM, et al (July 2008). Effectiveness of cetrorelix for the prevention of premature luteinizing hormone surge during controlled ovarian stimulation using letrozole and gonadotropins: a randomized trial. Fertil. Steril. 90: 113-120.
  6. ↑ La Marca, A.; Sunkara, S. K. (2013). “Individualization of controlled ovarian stimulation in IVF using ovarian reserve markers: From theory to practice”. Human Reproduction Update. 20 (1): 124–40. doi:10.1093/humupd/dmt037. PMID 24077980.
  7. ↑ Al-Inany, HG; Youssef, MA; Ayeleke, RO; Brown, J; Lam, WS; Broekmans, FJ (ngày 29 tháng 4 năm 2016). “Gonadotrophin-releasing hormone antagonists for assisted reproductive technology” (PDF). The Cochrane Database of Systematic Reviews. 4: CD001750. doi:10.1002/14651858.CD001750.pub4. PMID 27126581.
  8. ↑ Engel JB, Audebert A, Frydman R, et al (October 2007). Presurgical short term treatment of uterine fibroids with different doses of cetrorelix acetate: a double-blind, placebo-controlled multicenter study. Eur. J. Obstet. Gynecol. Reprod. Biol. 134: 225-232.
  9. ↑ Weiss JM, Diedrich K, Ludwig M (2002). Gonadotropin-releasing hormone antagonists: pharmacology and clinical use in women. Treat. Endocrinol. 1: 281-291.
  10. ↑ Debruyne F, Gres AA, Arustamov DL (July 2008). Placebo-controlled dose-ranging phase 2 study of subcutaneously administered LHRH antagonist cetrorelix in patients with symptomatic benign prostatic hyperplasia. Eur. Urol. 54: 170-177.
  11. ↑ Amory JK (March 2007). Contraceptive developments for men. Drugs Today (Barc.) 43: 179-192.
  12. ↑ Hembree WC, Cohen-Kettenis PT, Gooren L, Hannema SE, Meyer WJ, Murad MH, Rosenthal SM, Safer JD, Tangpricha V, T'Sjoen GG (tháng 11 năm 2017). “Endocrine Treatment of Gender-Dysphoric/Gender-Incongruent Persons: An Endocrine Society Clinical Practice Guideline”. J. Clin. Endocrinol. Metab. 102 (11): 3869–3903. doi:10.1210/jc.2017-01658. PMID 28945902.
  13. ↑ Randolph JF (tháng 12 năm 2018). “Gender-Affirming Hormone Therapy for Transgender Females”. Clin Obstet Gynecol. 61 (4): 705–721. doi:10.1097/GRF.0000000000000396. PMID 30256230.
  14. ↑ Wiik, Anna; Andersson, Daniel P.; Brismar, Torkel B.; Chanpen, Setareh; Dhejne, Cecilia; Ekström, Tomas J.; Flanagan, John N.; Holmberg, Mats; Kere, Juha (2018). “Metabolic and functional changes in transgender individuals following cross-sex hormone treatment: Design and methods of the GEnder Dysphoria Treatment in Sweden (GETS) study”. Contemporary Clinical Trials Communications. 10: 148–153. doi:10.1016/j.conctc.2018.04.005. ISSN 2451-8654. PMC 6046513. PMID 30023449.
  15. ↑ Aarthi Arasu (2016). “Clinical Vignette: Transgender Care”. Proceedings of UCLA Healthcare. 20. Bản gốc lưu trữ ngày 22 tháng 4 năm 2019. Truy cập ngày 28 tháng 1 năm 2021.
  16. ↑ http://adisinsight.springer.com/drugs/800032710
  17. ↑ Ezzati, Mohammad; Carr, Bruce R (2015). “Elagolix, a novel, orally bioavailable GnRH antagonist under investigation for the treatment of endometriosis-related pain”. Women's Health. 11 (1): 19–28. doi:10.2217/whe.14.68. ISSN 1745-5057. PMID 25581052.
  18. ↑ Serono. Cetrotide prescribing information 2009. Truy cập 18-6-2009.
  19. ↑ Degarelix US prescribing information 2008. Truy cập 28-4-2009.
  20. ↑ Organon. Ganirelix acetate prescribing information 2009. Truy cập 18-6-2009.
  21. ↑ Klotz L, Boccon-Gibod L, Shore ND, et al (December 2008). The efficacy and safety of degarelix: a 12-month, comparative, randomized, open-label, parallel-group phase III study in patients with prostate cancer. BJU. Int. 102: 1531-1538.
  22. ↑ Debruyne F, Bhat G, Garnick MB (December 2006). Abarelix for injectable suspension: first-in-class gonadotropin-releasing hormone antagonist for prostate cancer. Future Oncol. 2: 677-696.
  23. ↑ Broqua P, Riviere PJ, Conn PM, et al (April 2002). Pharmacological profile of a new, potent, and long-acting gonadotropin-releasing hormone antagonist: degarelix. J. Pharmacol. Exp. Ther. 301: 95-102.
  24. ↑ Engel JB, Schally AV (February 2007). Drug Insight: clinical use of agonists and antagonists of luteinizing-hormone-releasing hormone. Nat. Clin. Pract. Endocrinol. Metab.: 3: 157-167.
  25. ↑ Gustofson RL, Segars JH, Larsen FW (November 2006). Ganirelix acetate causes a rapid reduction in estradiol levels without adversely affecting oocyte maturation in women pretreated with leuprolide acetate who are at risk of ovarian hyperstimulation syndrome. Hum. Reprod. 21: 2830-2837.
  26. ↑ Mezo G, Manea M (tháng 12 năm 2009). “Luteinizing hormone-releasing hormone antagonists”. Expert Opin Ther Pat. 19 (12): 1771–85. doi:10.1517/13543770903410237. PMID 19939192.