نتایج جستجو برای: gonadotropin releasing hormone agonist

تعداد نتایج: 210153  

2014
Seyit Temel Ceyhan Yeşim Bayoğlu Tekin Mehmet Sakinci Cihangir Mutlu Ercan Uğur Keskin

OBJECTIVE Evaluation of the impact of agonist or antagonist protocol selection on pregnancy outcomes after failure of in-vitro fertilization (IVF) treatment cycles which were down regulated with Gonadotropin Releasing Hormone (GnRH) agonist. MATERIALS AND METHODS This was a retrospective study. Two hundred and sixty nine patients who were treated with GnRH agonist protocol between years 2002-...

2016
Ali Sami Gurbuz Funda Gode Mehmet Sukru Uzman Betul Ince Melek Kaya Necati Ozcimen Emel Ebru Ozcimen Ali Acar

BACKGROUND To evaluate the effects of an ovulation triggering agent, human chorionic gonadotropin (hCG), versus a gonadotropin-releasing hormone agonist (GnRHa) on early embryo development in vitro using a time-lapse system. METHODS Retrospective analysis of a prospectively collected database. A total of 739 embryos from 152 infertile couples undergoing intracytoplasmic sperm injection cycles...

حسینی, احمد , رئوفی, آزاده , عبدالهیان, پروانه , مهرافزا, مرضیه , نصیری, مهری , نیکپوری, زهرا ,

Background: Polycystic ovarian syndrome (PCOS) is the most common endocrinological disorders that affect approximately 5-7% of women in reproductive age. There is not any consensus about the efficient in vitro fertilization (IVF) protocol for patients with PCOS. The aim of the present study was to compare the half and one-third dose depot gonadotropin-releasing hormone (GnRH) agonist protocols ...

Journal: :Journal of Pediatric Endocrinology and Metabolism 2021

Abstract Objectives Gonadotropin-releasing hormone agonist treatment is important for optimal growth in girls with central precocious puberty (CPP). Data are lacking regarding benefit to height outcome when started after chronological age (CA) of 7 years, and if continued beyond CA 10 years or bone (BA) 12 years. Methods Forty-eight CPP were treated monthly leuprolide depot. Change predicted ad...

Journal: :Lijecnicki vjesnik 2011
Silvio Altarac

Long-acting synthetic luteinising hormone-releasing hormone agonists have become the mainstay for androgen-deprivation therapy, because they avoid the physical and psychological discomfort associated with orchidectomy and lack the potential cardiotoxicity associated with estrogens such as diethylstilbestrol. Currently available luteinising hormone-releasing hormone agonist analogues include leu...

Journal: :European journal of biochemistry 2003
Timothy C Cheung John P Hearn

A new baculovirus-based fluorescence resonance energy transfer (Bv-FRET) assay for measuring multimerization of cell surface molecules in living cells is described. It has been demonstrated that gonadotropin-releasing hormone receptor (GnRH-R) was capable of forming oligomeric complexes in the plasma membrane under normal physiological conditions. The mouse gonadotropin-releasing hormone recept...

2014
Chan-Yong Park Sun-Young Jung Kwang-Beom Lee Sun-Hye Yang

OBJECTIVE To assess the effects of a gonadotropin-releasing hormone agonist (GnRH-a) depot (Leuprolide acetate) in women with gynecologic cancer receiving chemotherapy while taking a continuous add-back on the prevention of premature ovarian failure. METHODS Fourteen premenopausal patients with gynecological malignancies who had undergone conservation of ovaries surgery received a GnRH-a depo...

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