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Titlebook: Medical Therapy in Urology; I. S. Shergill,Manit Arya,A.R. Mundy Book 2010 Springer-Verlag London 2010 cancer.care.erectile dysfunction.ho

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书目名称Medical Therapy in Urology
编辑I. S. Shergill,Manit Arya,A.R. Mundy
视频video
图书封面Titlebook: Medical Therapy in Urology;  I. S. Shergill,Manit Arya,A.R. Mundy Book 2010 Springer-Verlag London 2010 cancer.care.erectile dysfunction.ho
描述The future of urology is changing from one based around surgery, to an outpatient system, concentrating mainly on medical mana- ment. Last year, in the UK, there were almost two million hospital consultations for urological symptoms and an estimated fve million consultations in general practice. With such a signifcant proportion of care being delivered for urology, 80% of which can be managed medically, we felt that a resource should be made available to providers that will serve as a quick and useful guide to the medical management of urological disease. The aim was to provide a fresh, practical, and concise overview of the key medical management issues every practicing clinician faces in an outpatient urology setting, on a daily basis. With these goals in mind, each chapter starts with a brief overview of the relevant anatomy/physiology and pathology of the condition in question, and then goes on to give an explanation of the drugs used, including mode of action, doses, side effects, and important interactions/contraindications. Finally, there is a brief but relevant section on review of medical literature and a clinical section on when a particular drug treatment should be used.
出版日期Book 2010
关键词cancer; care; erectile dysfunction; hospital; incontinence; infection; management; pain; physiology; prostate
版次1
doihttps://doi.org/10.1007/978-1-84882-704-2
isbn_softcover978-1-84882-703-5
isbn_ebook978-1-84882-704-2
copyrightSpringer-Verlag London 2010
The information of publication is updating

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José M. Reyes,Michael A. Pontaricies in an attempt to model more accurately the in-vivo mineralization processes (9). Under physiological conditions, the low molecular weight ions appear to account for only 5–10% of the observed inhibition.
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William G. Robertsoncies in an attempt to model more accurately the in-vivo mineralization processes (9). Under physiological conditions, the low molecular weight ions appear to account for only 5–10% of the observed inhibition.
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Behdad Afzali,Kerem B. Atalar,Refik Gökmen,David J. A. Goldsmithin urine has been confined almost exclusively to the calcium phosphate and calcium oxalate crystal systems. Outlined in Table 2 are a list of the major inhibitors for these systems along with a concentration of the inhibitor required to cause 50% inhibition in the standard seeded crystal growth systems (5–7).
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