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1      Thirty-three patients had also received androgen therapy.
2 tations in telomerase genes can improve with androgen therapy.
3 ive androgen receptor modulators (SARMs) for androgen therapy.
4 ese androgen-independent tumors despite anti-androgen therapy.
5 ncer resistance to hormone-ablative and anti-androgen therapy.
6 ese mutations may be the best candidates for androgen therapy.
7 direct role in preventing resistance to anti-androgen therapy.
8  and restores responsiveness of CRPC to anti-androgen therapy.
9 s, associated genetic factors, or history of androgen therapy.
10  setting of advanced malignancies, high-dose androgen therapy, and Bartonella henselae infection.
11 w serum testosterone concentrations (bipolar androgen therapy [BAT]) in this setting might induce tum
12  blockade for prostate cancer prevention and androgen therapy for andropause treatment in elderly men
13          Our results provide a mechanism for androgen therapy in bone marrow failure: androgens appea
14  findings support the clinical evaluation of androgen therapy in the prevention and perhaps treatment
15 red physical changes from oestrogen and anti-androgen therapy include decreased body and facial hair,
16 drogens led to the development of novel anti-androgen therapies including abiraterone acetate and enz
17                                              Androgen therapy is used to compensate for low levels of
18 c stem cell transplantation is critical, and androgen therapy may be helpful.
19  cancers (PCs), initially responsive to anti-androgen therapies, often advance to a hormone-refractor
20 t the majority of patients treated with anti-androgen therapy progress to androgen-independence chara
21  through the transient generation of an anti-androgen therapy-resistant cell population, suggesting t

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