Endocrinologic and clinical evaluation following a single administration of a gonadotrophin-releasing hormone agonist (Zoladex**Goserelin, Imperial Chemical Industries Pharmaceuticals Division, Macclesfield, Cheshire, United Kingdom.), in a depot formulation, to premenopausal women

Author:

Matta Wassim H.M.,Shaw Robert W.,Burford Graham D.

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology,Reproductive Medicine

Reference6 articles.

1. Clinical applications of LHRH and its analogues;Sandow;Clin Endocrinol,1983

2. Treatment of patients with advanced cancer of the prostate using a slow-release (depot) formulation of the LHRH agonist ICI 118630 (Zoladex);Walker;J Endocrinol,1984

3. Preliminary endocrinological evaluation of a sustained-release formulation of the LH-releasing hormone agonist D-Ser (BUT)6 Azgly10 LHRH in premenopausal women with advanced breast cancer;Walker;J Endocrinol,1986

4. Reversible pituitary ovarian suppression induced by an LHRH agonist in the treatment of endometriosis: comparison of two dose regimens;Shaw;Clin Reprod Fertil,1986

5. Efficacy of different modalities of LHRH agonist (buserelin) administration on the inhibition of the pituitary-ovarian axis for the treatment of endometriosis;Lemay,1986

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