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孕早期黄体中期促性腺激素释放激素类似物的应用

Midluteal gonadotropin-releasing hormone analog administration in early pregnancy.

作者信息

Ron-El R, Golan A, Herman A, Raziel A, Soffer Y, Caspi E

机构信息

Department of Obstetrics and Gynecology, Assaf Harofeh Medical Center, Tel Aviv University, Israel.

出版信息

Fertil Steril. 1990 Mar;53(3):572-4. doi: 10.1016/s0015-0282(16)53361-5.

DOI:10.1016/s0015-0282(16)53361-5
PMID:2137797
Abstract

The incidence of GnRH-analog administration in the presence of undiagnosed pregnancy is discussed. Immediate hormonal supplementation avoids luteolysis. The report includes two cases, one without hormonal replacement, in which preclinical pregnancy occurred, and the second, where P was supplemented immediately upon diagnosis of pregnancy.

摘要

讨论了在未诊断出怀孕的情况下给予GnRH类似物的发生率。立即进行激素补充可避免黄体溶解。该报告包括两个病例,一个未进行激素替代,发生了临床前妊娠;另一个在诊断出怀孕后立即补充了孕激素。

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1
Midluteal gonadotropin-releasing hormone analog administration in early pregnancy.孕早期黄体中期促性腺激素释放激素类似物的应用
Fertil Steril. 1990 Mar;53(3):572-4. doi: 10.1016/s0015-0282(16)53361-5.
2
Follicular and luteal phase characteristics following early cessation of gonadotrophin-releasing hormone agonist during ovarian stimulation for in-vitro fertilization.在体外受精的卵巢刺激过程中,促性腺激素释放激素激动剂提前停用后的卵泡期和黄体期特征。
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Impaired corpus luteum function and other undesired results of pregnancies associated with inadvertent administration of a long-acting agonist of gonadotrophin-releasing hormone.
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Luteolytic effect of D-Trp6-luteinizing hormone-releasing hormone in the rhesus monkey (Macaca mulatta).D-色氨酸6-促黄体生成激素释放激素对恒河猴(猕猴)的溶黄体作用。
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Luteinizing response to human chorionic gonadotropin does not predict outcome in gonadotropin releasing hormone agonist-suppressed/human menopausal gonadotropin-stimulated in vitro fertilization (IVF) cycles.对人绒毛膜促性腺激素的促黄体生成素反应不能预测促性腺激素释放激素激动剂抑制/人绝经后促性腺激素刺激的体外受精(IVF)周期的结局。
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Induction of luteolysis by luteinizing hormone-releasing factor (LRF) agonist: sensitivity, reproducibility, and reversibility.
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A luteinizing hormone-releasing hormone agonist decreases biological activity and modifies chromatographic behavior of luteinizing hormone in man.促黄体生成素释放激素激动剂可降低人体促黄体生成素的生物活性并改变其色谱行为。
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Nonsupplemented luteal phase characteristics after the administration of recombinant human chorionic gonadotropin, recombinant luteinizing hormone, or gonadotropin-releasing hormone (GnRH) agonist to induce final oocyte maturation in in vitro fertilization patients after ovarian stimulation with recombinant follicle-stimulating hormone and GnRH antagonist cotreatment.在接受重组促卵泡激素和促性腺激素释放激素(GnRH)拮抗剂联合治疗进行卵巢刺激后的体外受精患者中,给予重组人绒毛膜促性腺激素、重组促黄体生成素或GnRH激动剂诱导最终卵母细胞成熟后,未补充黄体期的特征。
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The comparison of early follicular and midluteal administration of long-acting gonadotropin-releasing hormone agonist.长效促性腺激素释放激素激动剂在卵泡早期和黄体中期给药的比较。
Fertil Steril. 1990 Aug;54(2):233-7. doi: 10.1016/s0015-0282(16)53695-4.

引用本文的文献

1
Outcome of pregnancies inadvertently exposed to gonadotropin-releasing hormone analogues (GnRH-a) in early gestation.妊娠早期意外暴露于促性腺激素释放激素类似物(GnRH-a)的妊娠结局。
J Assist Reprod Genet. 1993 Aug;10(6):437-9. doi: 10.1007/BF01228095.
2
Inadvertent exposure of early pregnancy to gonadotropin releasing hormone analogue.妊娠早期意外暴露于促性腺激素释放激素类似物。
J Assist Reprod Genet. 1993 Jul;10(5):387-91. doi: 10.1007/BF01213438.