نتایج جستجو برای: decapeptyl

تعداد نتایج: 30  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2005
Gunhild Keller Andrew V Schally Timo Gaiser Attila Nagy Benjamin Baker Gabor Halmos Jörg B Engel

PURPOSE To determine the expression of luteinizing hormone releasing hormone (LHRH) receptors in specimens and cell lines of human renal cell carcinoma (RCC) and to evaluate the antitumor efficacy of targeted therapy with a cytotoxic analogue of LHRH, AN-207, in vivo. AN-207, consisting of [D-Lys(6)] LHRH linked to a cytotoxic radical, 2-pyrrolinodoxorubicin (AN-201), binds with high affinity t...

Journal: :Human Reproduction 2023

Abstract Study question Is there an advantage for modified flare/ GnRH antagonist protocol in comparison to oocyte cryopreservation cycles? Summary answer Modified is at least as good cycles, potentially improving maturity rate subgroup of patients. What known already Ultrashort flare agonist (GnRHa)/GnRH -antagonist offer benefits stimulatory effect repeated microdose on endogenous FSH and the...

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: :Clinical cancer research : an official journal of the American Association for Cancer Research 2003
Markus Letsch Andrew V Schally Karoly Szepeshazi Gabor Halmos Attila Nagy

PURPOSE AND EXPERIMENTAL DESIGN To improve conventional chemotherapy, we developed cytotoxic analogues of luteinizing hormone-releasing hormone (LH-RH), which can be targeted to prostate cancers expressing LH-RH receptors. In view of pending clinical trials on cytotoxic LH-RH analogue AN-152, containing doxorubicin (DOX) linked to [D-Lys(6])-LH-RH, we investigated the effects of AN-152 on tumor...

Journal: :Human reproduction 1998
J Bódis A Török J Garai Z Bognár I Szabó H R Tinneberg

Preovulatory rise in progesterone Dear Sir, We read with great interest the article by Eldar-Geva et al. (1998). In the late follicular phase of gonadotrophin-releasing hormone (GnRH) agonist/human menopausal gonadotrophin (HMG)-stimulated cycles they showed a concomitant increase of serum progesterone and luteinizing hormone (LH), both of which were reversible by the administration of dexameth...

2000
J. Itskovitz - Eldor S. Kol B. Mannaerts

longer half-life [ 24 h versus 60 min for LH (Yen et al., A new treatment option for patients undergoing ovarian 1968; Damewood et al., 1989)], HCG administration results stimulation is the gonadotrophin-releasing hormone in a prolonged luteotrophic effect, characterized by the develop(GnRH) antagonist protocol, with the possibility to trigger ment of multiple corpora lutea and supraphysiologic...

2005
Amany Shaltout Amal Shohayeb Adel Faruk Mohamad Eid Mona Mostafa Ashraf Eldaly Samir Abbas

Objective: To detect the effect of late coasting on oocyte quality. Design: Retrospective study. Setting: Samir Abbas Medical Center Materials and methods: Patients where estradiol level was over 4000 pg/ml and late coasting was used as a method to prevent OHSS, and patients where estradiol level was over 4000 pg / ml but no coasting was done Main outcome measure(s) : Oocyte quality. Results: n...

2013
Faiz A. Alwaeely Faiz Abdulwahid Alwaeely

The aim of this study is to compare clinical pregnancy rates in ICSI-ET cycles where GnRH agonist or hCG was used to induce final maturation of the oocytes. A total of 97 women who produced more than 14 follicles following ovulation induction with recombinant FSH and GnRH antagonist were selected for randomization. Human chorionic gonadotropin (hCG, 5.000 IU, IM) or GnRH agonist (triptorelin 0....

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