The 5 alpha-reductase inhibitor, finasteride, provides a logical medical treatment for benign prostatic hyperplasia (BPH). However, the effects of chronic finasteride treatment on prostatic androgen levels, 5 alpha-reductase activity and tissue prostatic specific antigen (PSA) have not been studied. We have examined prostate tissue androgen concentrations and 5 alpha-reductase activity of the gland in men with BPH treated with the drug for 3 months
PURPOSE: Finasteride is an inhibitor of human 5alpha-reductase, which results in a decrease in plasm...
5α-reductase 1 (5αR1) and 5α-reductase 2 (5αR2) convert testosterone into the more potent androgen d...
The use of the 5-alpha reductase inhibitors (5-ARIs) finasteride and dutasteride for prostate cancer...
The development and introduction in clinical practice of finasteride, the first potent inhibitor of ...
Effect of long-term administration of finasteride (MK-906), an inhibitor of 5 alpha-reductase, in pa...
Finasteride is a drug used in treatment men with benign prostatic hyperplasia (BPH), blocks the acti...
The development and introduction in clinical practice of finasteride, the first potent inhibitor of ...
Finasteride is primarily used to treat benign prostatic hyperplasia (BPH) and male androgenetic alop...
ObjectiveTo evaluate the effect of finasteride on serum androst-4-ene-3,17-dione (androstenedione) a...
In humans, androgens balance cell proliferation and apoptosis, ensuring normal growth and developmen...
BACKGROUND: Although finasteride is recognized for its role as a chemopreventive agent for prostate ...
Abstract: Finasteride is the 5α-reductase inhibitor that received clinical approval for the treatmen...
7-alpha-Methyl-19-Nortestosterone (MENT) is a synthetic androgen more potent than testosterone (T) ...
Introduction: Finasteride is a 5-alpha-reductase inhibitor used in the medical treatment of benign p...
Objective: To evaluate the effect of finasteride on serum androst-4-ene-3,17-dione (androstenedione)...
PURPOSE: Finasteride is an inhibitor of human 5alpha-reductase, which results in a decrease in plasm...
5α-reductase 1 (5αR1) and 5α-reductase 2 (5αR2) convert testosterone into the more potent androgen d...
The use of the 5-alpha reductase inhibitors (5-ARIs) finasteride and dutasteride for prostate cancer...
The development and introduction in clinical practice of finasteride, the first potent inhibitor of ...
Effect of long-term administration of finasteride (MK-906), an inhibitor of 5 alpha-reductase, in pa...
Finasteride is a drug used in treatment men with benign prostatic hyperplasia (BPH), blocks the acti...
The development and introduction in clinical practice of finasteride, the first potent inhibitor of ...
Finasteride is primarily used to treat benign prostatic hyperplasia (BPH) and male androgenetic alop...
ObjectiveTo evaluate the effect of finasteride on serum androst-4-ene-3,17-dione (androstenedione) a...
In humans, androgens balance cell proliferation and apoptosis, ensuring normal growth and developmen...
BACKGROUND: Although finasteride is recognized for its role as a chemopreventive agent for prostate ...
Abstract: Finasteride is the 5α-reductase inhibitor that received clinical approval for the treatmen...
7-alpha-Methyl-19-Nortestosterone (MENT) is a synthetic androgen more potent than testosterone (T) ...
Introduction: Finasteride is a 5-alpha-reductase inhibitor used in the medical treatment of benign p...
Objective: To evaluate the effect of finasteride on serum androst-4-ene-3,17-dione (androstenedione)...
PURPOSE: Finasteride is an inhibitor of human 5alpha-reductase, which results in a decrease in plasm...
5α-reductase 1 (5αR1) and 5α-reductase 2 (5αR2) convert testosterone into the more potent androgen d...
The use of the 5-alpha reductase inhibitors (5-ARIs) finasteride and dutasteride for prostate cancer...