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  6. otrezal New Member

    JAMAJAMA Network Open JAMA Cardiology JAMA Dermatology JAMA Facial Plastic Surgery JAMA Internal Medicine JAMA Neurology JAMA Oncology JAMA Ophthalmology JAMA Otolaryngology–Head & Neck Surgery JAMA Pediatrics JAMA Psychiatry JAMA Surgery Archives of Neurology & Psychiatry (1919-1959) Fisher B, Costantino JP, Wickerham DL. Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study. 1998;71-13889747868Google Scholar Crossref Powles T, Eeles R, Ashley S. Interim analysis of the incidence of breast cancer in the Royal Marsden Hospital tamoxifen randomised chemoprevention trial. 1998;3-1019672274Google Scholar Cuzick J, Forbes J, Edwards R. First results from the International Breast Cancer Intervention Study (IBIS-I): a randomised prevention trial. 2002;37-82412243915Google Scholar Crossref Veronesi U, Maisonneuve P, Costa A. Differential effects of raloxifene, tamoxifen and fulvestrant on a murine mammary carcinoma. 2003;-3512779079Google Scholar Crossref Gottardis MM, Ricchio ME, Satyaswaroop PG, Jordan VC. Prevention of breast cancer with tamoxifen: preliminary findings from the Italian randomised trial among hysterectomised women. Role of raloxifene in breast cancer prevention in postmenopausal women: clinical evidence and potential mechanisms of action. 2004;0-84015262454Google Scholar Crossref Lamb CA, Helguero LA, Fabris V, Lucas C, Molinolo AA, Lanari C. Effect of steroidal and nonsteroidal antiestrogens on the growth of a tamoxifen-stimulated human endometrial carcinoma (En Ca101) in athymic mice. 1990;89-31922334915Google Scholar Delmas PD, Bjarnason NH, Mitlak BH. Effects of raloxifene on bone mineral density, serum cholesterol concentrations, and uterine endometrium in postmenopausal women. 1997;341-16479385122Google Scholar Crossref Lippman ME, Krueger KA, Eckert S. Indicators of lifetime estrogen exposure: effect on breast cancer incidence and interaction with raloxifene therapy in the multiple outcomes of raloxifene evaluation study participants. 2001;11-3116Cummings SR, Duong T, Kenyon T, Cauley JA, Whitehead M, Krueger KA. Multiple Outcomes of Raloxifene Evaluation (MORE) Trial. Bone mineral density and risk of breast cancer in older women: The Study of Osteoporotic Fractures. 1996;204-14088892715Google Scholar Crossref Martino S, Cauley JA, Barrett-Connor E. Continuing Outcomes Relevant to Evista: breast cancer incidence in postmenopausal osteoporotic women in a randomized trial of raloxifene. 2004;51-176115572757Google Scholar Crossref Kleinman D, Karas M, Danilenko M. Stimulation of endometrial cancer cell growth by tamoxifen is associated with increased insulin-like growth factor (IGF)-I induced tyrosine phosphorylation and reduction in IGF binding proteins. 1996;189-10958603578Google Scholar Crossref Gail MH, Brinton LA, Byar DP. Projecting individualized probabilities of developing breast cancer for white females who are being examined annually. 1989;79-18862593165Google Scholar Crossref Vogel VG, Costantino JP, Wickerham DL, Cronin WM, Wolmark N. Serum estradiol level and risk of breast cancer during treatment with raloxifene. 2002;26-22011779264Google Scholar Crossref Cauley JA, Norton L, Lippman ME. Continued breast cancer risk reduction in postmenopausal women treated with raloxifene: 4-year results from the MORE trial. 2001;5-13411261828Google Scholar Crossref Ettinger B, Black DM, Mitlak BH. Multiple Outcomes of Raloxifene Evaluation Investigators. Reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: results from a 3-year randomized clinical trial. 1999;27-64510517716Google Scholar Crossref Cauley JA, Lucas FL, Kuller LH. The study of tamoxifen and raloxifene: preliminary enrollment data from a randomized breast cancer risk reduction trial. 2002;3-15912123540Google Scholar Crossref Vogel VG, Costantino JP, Wickerham DL, Cronin WM. National Surgical Adjuvant Breast and Bowel Project update: prevention trials and endocrine therapy of ductal carcinoma in situ. 2003;5S-501S12538506Google Scholar Mc Horney CA, Ware JE Jr, Lu JF, Sherbourne CD. The MOS 36-item Short-Form Health Survey (SF-36), III: tests of data quality, scaling assumptions, and reliability across diverse patient groups. 1994;-668277801Google Scholar Crossref Mc Horney CA, Ware JE Jr, Raczek AE. Watch for Ocular Effects of Breast Cancer Drugs - American. cialis 120 Tamoxifen and Cataracts A Null Association Request PDF Precautions and Warnings With Tamoxifen
     
  7. alex1968 User

    Des Spence’s polemic about duloxetine [1] loses most of its power because almost every assertion he makes is wrong. Using references to support a point of view doesn’t help much when they out-of-date and superseded by new knowledge or more relevant evidence. We assume that it is not ignorance of the arguments but a deliberate attempt to provoke, despite the reasoned arguments of science. It succeeded in this because the management of chronic pain is important irrespective of what the pharma industry says. The research is dense and complex, but we know an increasing amount about the bio-psycho-social origins of pain. Research in genetics, neurobiology, and imaging have established how astonishingly complex acute and chronic pain can be; the brains of people with chronic pain are very different from those of us lucky enough not to have it. Without wanting to be comprehensive, here is a brief list of where Spence misses the point: Medicalising of chronic pain. Duloxetine More Effective at Treating Neuropathic Pain inderal used for anxiety New Study Duloxetine Effective in Treating Fibromyalgia – National. Duloxetine - The British Pain Society
     
  8. lio-seo New Member

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