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爱普列特在治疗良性前列腺增生中的应用 被引量:9

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出处 《现代泌尿外科杂志》 CAS 2006年第4期246-248,共3页 Journal of Modern Urology
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参考文献26

  • 1McConnell JD. Epidemiology, etiology, pathophysiology, and diagnosis of benign prostatic hyperplasia. In:Walsh PC, Sfamey TA. Campbell's Urology [M]. 7th ed. Philadelphia: Saunders, 1998:1429-1452.
  • 2McConnell JD, Roehrborn CG, Bautista OM, et al. The long- term effect of doxazosin, finasteride, and combination therapy on the clinical progression of benign prostatic hyperplasia [J].N Engl J Med, 2003, 349(25) :2387-2398.
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  • 4Chen W, Zouboulis CC, Fritsch M, et al. Evidence of heterogeneity and quantitative differences of the type 1 5alpha-reductase expression in cultured human skin cells-evidence of its presence in melanocytes [J]. J Invest Dermatol, 1998, 110(1):84-89.
  • 5Yokoi H, Tsuruo Y, Miyamoto T, et al. Steroid 5 alpha-reductase type 1 immunolocalized in the adrenal gland of normal, gonadectomized, and sex hormone-supplemented rats [J]. Histochem Cell Biol, 1998, 109(2):127-134.
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  • 7左韬,王建业.细胞凋亡:良性前列腺增生发病机制的新探索[J].中华泌尿外科杂志,1999,20(8):508-510. 被引量:7
  • 8Hudson PB, Boake R, Trachtenberg J, et al. Efficacy of finasteride is maintained in patients with benign prostatic hyperplasia treated for 5 years. The North American Finasteride Study Group [J]. Urology, 1999, 53(4) :690-695.
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二级参考文献25

  • 1鲍镇美.细胞凋亡与疾病[J].中日友好医院学报,1994,8(3):175-178. 被引量:4
  • 2邓方明,顾方六,夏同礼.癌蛋白bcl-2在前列腺增生组织中的表达及其意义[J].中华泌尿外科杂志,1995,16(12):729-731. 被引量:13
  • 3张学军,Chung Lee,Carl Olsson,Ralph Buttyan,马腾骧.bcl-2 基因在良性前列腺增生中的作用[J].中华泌尿外科杂志,1997,18(2):97-99. 被引量:15
  • 4[1]Audet. PH., Lamb Y, Jorkasky D, et al. Effect of multiple doses of epristends, a steroid 5a- reductase inhibitor, on serum dihydrotestos- terone in older male subjects. Clin Pharmacol Ther, 1993; 53: 231.
  • 5[2]Johnsonbaugh RE, Cohen BR, McCormack, EM, et al. Effect of fourteen days treatment with epristeride, an uncompetitive 5a- reductase inhibitor. on serum and prostatic testosterone and dihydrotestosterone in men with benign prostatic hyperpiasia. J Urol, 1993; 149: 423a.
  • 6[3]Depre M, Meeter C, Hecken AV, et al. Pharmacodynamics and tolerability of L-654,066, a steroid 5a- reductase inhibitor, in men. Clin Pharmacol Ther, 1992; 52: 409~412.
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