Etienne Marbaix
The Catholic University of America
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Human Reproduction | 1996
Françoise Casanas-Roux; Michelle Nisolle; Etienne Marbaix; Mireille Smets; Salim Bassil; Jacques Donnez
Recently advanced computerized technology was applied to the investigation of morphometric, immunohistological and three-dimensional changes of the endometrial mucosa in order to evaluate quantitatively the effects of three doses of a new slow-release vaginal progesterone on the endometrium in post-menopausal women. A total of 20 menopausal women, deprived of ovarian function, were given oestrogen for 12 days and a combined therapy of oestrogen (administered orally) and progesterone for another 12 day period. Progesterone was administered vaginally through a new gel (Crinone) utilizing a bioadhesive, biocompatible polymer as a base to achieve a sustained release effect. An endometrial biopsy was taken before treatment, after oestrogen-only treatment and after the oestro-progestogen therapy. Before treatment, all the patients exhibited an atrophic endometrium. After oestrogen-only treatment, typical proliferative changes occurred: an increase in the endometrium thickness, an increase in the mitotic index, numerous cylinder-like glands and no coiled glands, and high concentrations of oestrogen receptors (ER) and progesterone receptors (PR). After the oestro-progestogen therapy, whatever the dose of progesterone given, a secretory transformation of the endometrial mucosa occurred, mitotic activity decreased significantly, more ramified and coiled glands were observed, and a decrease in PR content was noted in epithelial and stromal nuclei, and a decrease in PR content was also observed in epithelial nuclei but not in stromal nuclei. Accurate new techniques of image analysis have shown that crinone therapy could eliminate the proliferative effects of oestrogen treatment in post-menopausal women, despite doses as low as 45 mg of progesterone administered vaginally every other day. The results suggest that the sustained release effects of Crinone are clinically relevant.
Metalloproteinases In Medicine | 2015
Hervé Emonard; Etienne Marbaix
License. The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. Permissions beyond the scope of the License are administered by Dove Medical Press Limited. Information on how to request permission may be found at: http://www.dovepress.com/permissions.php Metalloproteinases In Medicine 2015:2 9–18 Metalloproteinases In Medicine Dovepress
Archive | 2004
Patricia B. Cornet; Christine Galant; Yves Eeckhout; Pierre J. Courtoy; Etienne Marbaix; Patrick Henriet
Archive | 2014
Antoine Cominelli; Héloïse P. Gaide Chevronnay; Pascale Lemoine; Pierre J. Courtoy; Etienne Marbaix; Patrick Henriet
5th European Network of Immunology Institutes Summer School in advanced Immunology | 2010
Antoine Cominelli; Héloïse P. Gaide Chevronnay; Pierre J. Courtoy; Patrick Henriet; Etienne Marbaix
Archive | 2009
Charlotte Selvais; Héloïse P. Gaide Chevronnay; Pascale Lemoine; Stéphane Dedieu; Patrick Henriet; Pierre J. Courtoy; Etienne Marbaix; Hervé Emonard
Archive | 2009
Chrystel Pretto; Héloïse P. Gaide Chevronnay; Etienne Marbaix
Archive | 2009
Héloïse P. Gaide Chevronnay; Etienne Marbaix
21st Congress of the Federation of European Connective Tissue Societies | 2008
Antoine Cominelli; Héloïse P. Gaide Chevronnay; Pierre J. Courtoy; Patrick Henriet; Etienne Marbaix
Reproduction Humaine et Hormones | 2007
Jean-Luc Brun; Christine Galant; Dominique Dallay; Etienne Marbaix