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Finasteride generica funciona (Boeckh- et al., 2002). To test the relationship, we first asked two questions: whether the sex-ratio dependence of effects obtained by the three different chemical structures is consistent or not, and in which direction are the sex-ratio effects more pronounced that are seen in these other drugs. We also investigated whether there is an association between the dose-effect curve and gender of the active compound or whether there might be one for the compounds with similar structures but differing chemical structures. METHODS This study uses data obtained from the German Study Group on Aromatase Inhibitors in Male-to-Female Transsexuals that had undergone gonadectomy and the study group on clomiphene citrate in female-to-male transsexuals. The data on treatment in two studies represent the results obtained during 4 yr. Study design In the study on gonadectomy, patients (23 females and 12 males) were given hormonal therapy Nifedipine to buy based on the protocol recommended by a German physician, and received the GnRH agonists: clomiphene citrate (75–100 mg daily), gonadotropins (syntocin and undecanoate), 17β-estradiol. Among the patients who did not use hormonal therapy, a fixed dosage for clomiphene citrate were prescribed (100 mg daily). In the study on female-to-male transsexuals, patients (2 females and 1 male) were given GnRH agonist plus testosterone cream with an aim to produce female puberty. Clomiphene citrate was provided in doses of 10-50 mg daily. Two hundred and thirty patients enrolled in both studies; total, 119 patients received clomiphene citrate, and 89 patients received GnRH agonist plus testosterone. The mean age of patients was 42 years (range = 16–67 years). In both studies, 40 patients (32 males and 7 females) began treatment with testosterone cream, and 40 patients (27 males 7 avodart 0.5 mg buy females) began treatment with GnRH. All the patients received an initial 3-month double-blind phase. In addition to hormonal therapy, a mean of 14 h hormone therapy was also given. In each study, patients entered their own treatment protocol and continued in it until they reached the end of their treatment. However, if the end of treatment was indicated, patients were given a follow-up questionnaire. All the patients had an excellent baseline history, were not taking substances with an effect on sexual function, and underwent a physical examination. Patients were divided into three groups based on their gender assignment before the start of hormones, as well on their duration of androgen status before hormone-treatment. Assessments Participants were asked to report with whom they regularly have intercourse at least every day and also if they had any sexual relationship outside the study. Each patient was also asked about sexual satisfaction. They were also asked about their masturbation habits and ability to reach spontaneous emission. All the patient's medical history was obtained from a general practitioner, and in addition from a gynecologist, plastic surgeon, psychiatrist, and psychologist. In addition, the patients underwent a physical examination (table 1). Table 1. Anthropometry (mean ± SD), BMI body fat (mean ± SD) and percent blood testosterone (mean ± SD) of study participants a. Body height: 1.86 ± 0.12 m; pdfc partnership for a drug free canada a. Body weight: 53.7 ± 5 cm; b. Body height: 1.77 ± 0.06 m;

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