预订 Hereditary Tyrosinemia 9783319557793
海外仓库发货,通常付款后4-9周到货!
/ 2017-08-10
图书信息 书号: 9783319557793 作者: Robert M Tanguay 装帧: 精装 页数: 247页 出版社: Springer International Publishing 尺寸: 25.4 x 17.8 x 2.5 cm 出版日期: 2017-08-10 重量: 454g 语种: 其它(含多语) 内容简介 Hereditary tyrosinemia type 1 (HT1), the most severe i
¥2140
【预订】Reflective Writing for Nursing, Health and Social Work 9
美国库房发货,通常付款后3-5周到货!
/ 2020-04-15
Product Details 基本信息 ISBN-13 书号 9781352009965 Author 作者 Elizabeth Tanguay Format 版本 平装-胶订 Pages Number 页数 200页 Publisher 出版社 Red Globe Press Publication Date 出版日期 2020-04-15 Language 语种 英语 Book Contents 内容简介 This book takes students step-by-step through the process of planning and writing a reflective essay, beginning with crucial guidance on planning and structure. It introduces different reflective frameworks and shows readers how to structure a piece of writing according to a particular framework. Chapters contain a wealth of activities and exercises which will help build students’ skills and confidence. Suitable for students of all health-related disciplines in which written assignments requiring reflective practice are required.
¥246.00
【预订】Aging, Cancer and Age-Related Diseases - Common Mechanis
美国库房发货,通常付款后3-5周到货!
/ 2010-08-20
Product Details 基本信息 ISBN-13 书号 9781573317962 Author 作者 Robert M. Tanguay Format 版本 平装-胶订 Pages Number 页数 300页 Publisher 出版社 Wiley-Blackwell Publication Date 出版日期 2010-08-20 Language 语种 英语 Book Contents 内容简介 This volume recognizes the rapidly expanding research linking aging, age-related diseases, and the delicate balance between neurodegeneration and cancer. Wide perspectives on aging are covered, ranging from metabolic and cellular interventions in aging, o
¥1166
【预订】Hereditary Tyrosinemia 9783319857459
美国库房发货,通常付款后3-5周到货!
/ 2018-08-12
Product Details 基本信息 ISBN-13 书号 9783319857459 Author 作者 Robert M. Tanguay Format 版本 平装-胶订 Pages Number 页数 247页 Publisher 出版社 Springer Berlin Heidelberg Publication Date 出版日期 2018-08-12 Language 语种 英语 Book Contents 内容简介 Hereditary tyrosinemia type 1 (HT1), the most severe inborn error of the tyrosine degradation pathway, is due to a deficiency in fumarylacetoacetate hydrolase (FAH). The worldwide frequency of HT1 is one per 100,000 births, but some regions have a significantly higher incidence (1:1,800). The FAH defect results in the accumulation of toxic metabolites, mainly in the liver. If left untreated, HT1 is usually fatal before the age of two. HT1 patients develop several chronic complications including cirrhosis with a high risk of hepatocellular carcinoma (HCC) and neuropsychological impairment. Treatment comprises an inhibitor of the pathway, Nitisinone, a strict
¥1703
【预订】Hereditary Tyrosinemia: Pathogenesis, Screening and Mana
美国库房发货,通常付款后3-5周到货!
/ 2017-08-10
/ Springer
¥1670
【预订】Heroes vs. Villains/Space Chase! (DC Super Friends)
预订商品,需要1-3个月发货,非质量问题不接受退换货。
/ 2013-01-08
¥54.20