نتایج جستجو برای: cetrorelix acetate

تعداد نتایج: 50203  

2015
Anita Kåss Ivana Hollan Morten Wang Fagerland Hans Christian Gulseth Peter Abusdal Torjesen Øystein Torleiv Førre Cornelis B Lambalk

OBJECTIVES Gonadotropin-releasing hormone (GnRH) and pituitary gonadotropins, which appear to be proinflammatory, undergo profound secretory changes during events associated with rheumatoid arthritis (RA) onset, flares, or improvement e.g. menopausal transition, postpartum, or pregnancy. Potential anti-inflammatory effects of GnRH-antagonists may be most pronounced in patients with high GnRH an...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2000
M Schwahn H Schupke A Gasparic D Krone G Peter R Hempel T Kronbach M Locher W Jahn J Engel

Disposition and metabolism of cetrorelix was studied in intact and bile duct-cannulated rats and dogs after s.c. injection. An s.c. dose of 0.1 mg/kg [(14)C]cetrorelix was rapidly and completely absorbed in rats. T(max) in plasma and most tissues was at 2 h. Radioactivity at the injection site in rats declined to 10% by 24 h. The extent of (14)C absorption in rats calculated from excretion unti...

2017
Ayman S. Dawood Adel Algergawy Ahmed Elhalwagy

Objective To determine whether reducing the cetrorelix dose in the antagonist protocol to 0.125 mg had any deleterious effects on follicular development, the number and quality of retrieved oocytes, or the number of embryos, and to characterize its effects on the affordability of assisted reproductive technology. Methods This randomized controlled study was conducted at the Fertility Unit of ...

2016
FATEMEH NIKPOUR JAFAR SOLEIMANI RAD

Drugs which are used in chemotherapy to cure cancer, generated destruction effects in sensitive of organs as testies. These substances are disrupted Spermatogenesis. The aim of this Study is investigating protective effects of cetrorelix from side effects of Vincristine. 30 adult male mice were divided into 3 equal groups as: control, vincristine (V) and vincristine + cetrorelix (V+C) groups. A...

2016
Usama M. Fouda Ahmed M. Sayed Hesham S. Elshaer Bahaa Eldin M. Hammad Mona M. Shaban Khaled A. Elsetohy Mohamed A. Youssef

BACKGROUND The aim of this study was to compare the efficacy of antagonist rescue protocol (replacing GnRH agonist with GnRH antagonist and reducing the dose of gonadotropins) combined with cabergoline versus cabergoline alone in the prevention of ovarian hyperstimulation syndrome (OHSS) in patients pretreated with GnRH agonist long protocol who were at high risk for OHSS. METHODS Two hundred...

Journal: :Reproductive BioMedicine Online 2002

Journal: :Human Reproduction Update 2000

Journal: :Human reproduction 2007
Susheel Vani Sarah E McDonald Alistair R W Williams J Ian Mason K Joo Thong Hilary O D Critchley

BACKGROUND There are concerns of reduced pregnancy rates with the use of gonadotrophin-releasing hormone antagonists (GnRH antagonists) in IVF/ICSI cycles. Sex steroids and their metabolizing enzymes in the endometrium may play a vital role in embryo implantation. This study has evaluated the levels and localization of sex-steroid receptors and metabolizing enzymes, 3beta-hydroxysteroid dehydro...

Journal: :The Journal of clinical endocrinology and metabolism 2001
L Devoto P Kohen R R Gonzalez O Castro I Retamales M Vega P Carvallo L K Christenson J F Strauss

The expression of the steroidogenic acute regulatory protein (StAR) in the human corpus luteum (CL) was examined throughout the luteal phase. The primary 1.6-kb StAR transcript was in greater abundance in early (3.1-fold) and mid (2.2-fold) luteal phase CL compared with late luteal phase CL. The larger StAR transcript (4.4 kb) was found in early and midluteal phase CL, but was not detected in l...

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