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良性前列腺增生症的药物治疗进展 被引量:6

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作者 罗择庆
出处 《右江民族医学院学报》 2009年第3期491-493,共3页 Journal of Youjiang Medical University for Nationalities
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参考文献18

  • 1McConnell JD,Reginald B,Waish P,et al.The effect of finasteride on the risk of acute urinary retention and the need for surgical treatment among men with benign prostatic hyperplasia.Finasteride Long-Term Efficacy and Safety study Group[J].N Engl J Med,1998,338(9):557-563.
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  • 3Bartsch G,Rittmaster RS,Klocker H.Dihydrotestosterone and the concept of 5α-reductase inhibition in human benign prostatic hyperplasia[J].world J Urol,2002,19(6):413-425.
  • 4MeConnell JD.Androgen suppression in the management of benign prostatic hyperplasia[M]//Lepor H eds.Prostatic Diseases[J].Philadelphia:Saunders,2001:308-320.
  • 5Stuart JD,Lee FW,Simpson-Nod D,et al.Pharmacokinetic parameters and mechanisms of inhibition of rat type 1 and 2 steroid 5 alpha-reductases:determinantsfor different in vivo activities of GI198745 and finasteride in the rat[J].Biochem Pharmacol,2001,62(7):933-942.
  • 6Andriole GL,Kirby R.Safery and tolerability of the dual 5α-reductase inhibitor dutasteride in the treatment of benign prostatic hyperplasia[J].Eur Urol,2003,44(1):82-83.
  • 7Andriole G,Ray P,Gumphrey P,et al.The impact of dutasteride,a novel 5 alpha-reductase inhibitor on serum and intraprostatic anddrogens.Proceedings of the 2nd Wodd Congress on Men's Health[C].2002:30.
  • 8Clark R,Hermann D,Gabriel H,et al.Effective auppreasion of dihydrotestosterone(DHT)by GI198745,a noval,dual 5 alpha reductase inhibitor[J].J Urol,1999,161:1037.
  • 9Clark RV.Marked suppression of dihydrotestosterone (DHT)by dutasteride has no adverse effect on spermatogenesis in healthy men[J].Br J Urol,2002,90(suppl 2):14.
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二级参考文献11

  • 1保列治片[J].中国新药杂志,1995,4(3):13-13. 被引量:2
  • 2Rhodes PR, Krogh RH, Bruskewitz RC. Impact of drug therapy on benign prostatic hyperplasia-specifie quality of life. Urology 1999; 53(2): 1090-1098.
  • 3Hieble JP, Bylund DB, Clarke DE, et al. International union of pharmacology X.recommendation for nomenclature of α 1-adrenceptors consensus update. Pharmacol Rev 1995; 47(2): 267-269.
  • 4Nasu K, Moriyama N, Fukasawa R, et al. Quantification and distribution of α 1-adrenceptor subtype mRNAs in human proximal urethra. Br J Phramacol 1998; 123 (7):1289-1293.
  • 5Takei R, Ikegaki I, Shibata K, et al. Naftopidil, a novel α1-adrenceptor antagonist, displays selective inhibition of canine prostatic pressure and high affinity binding to cloned human α 1-adrenceptors. Jpn J Phamacol 1997;79(4): 447-454.
  • 6Niebch G, Locher M, Borbe HO. Metabolic fate of the novel antihypertensive drug naftopidil. Arzneimittelforschung 1991; 41(10): 1027-1032.
  • 7Takagi N, Ishii M, Takeda K, et al. Pharmacokinetics of naftopidil (KT-611) in hypertensive patients with renal impairment or normal renal function. J Clin Ther Med 1992; 8(3): 109-122.
  • 8Farthing MJ, Alstead EM, Abrams SM, et al, Pharmacokinetics of naftopidil, a novel anti-hypertensive drug,in patients with hepatic dysfunction. Postgrad Med J 1994; 70 (2):363-366.
  • 9Yasuda K, Yamanishi T, Tojo M, et al. Effrct of naftopidil on urethral obstruction in benigh prostatic hyperplasia;assessment by urodynamic studies. Prostate 1994; 25(1): 46-52.
  • 10何志嵩,金杰,那彦群,郭应禄.α受体阻滞剂对良性前列腺增生患者症状的影响作用[J].中华泌尿外科杂志,2002,23(6):358-360. 被引量:19

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