维普期刊资源整合服务平台（V6.5）

维普中文期刊产品整合服务

8篇 您的检索式：作者名="Pickardt"

选中清除导出查看参考文献查看引证文献引用追踪共1页首页上一页第1页下一页末页 /1 跳转

		题名	作者	年代	出处	被引量
	1	Mercury and arsenic bioaccumulation and eutrophication in Baiyangdian Lake, China 显示文摘	Chen C Y Pickardt P C Xu M Q	2008	Water Air and Soil Pollut2008，190，14：	1
	2	Computed tomograPhic virtual Colonoseopy to screen for colorectal neoplasia in asymptomatic adults显示文摘	Pickardt PJ choi JRC Hwang I	2003	N Eng J Med2003，349，21：	1
	3	Mercury and arsenic bioaccu-mulation and eutrophication in Baiyangdian Lake,China显示文摘	Chen C Y Pickardt P C Xu M Q	2008	Water Air and Soil Pollution2008，190，1：	1
	4	Processing of low polyphenol protein isolates from residues of sunflower seed oil production显示文摘	Pickardt C Weisz G M Eisner P	2011	Procedia Food Science2011，1，0：	1
	5	显示文摘	Bommer M Eversmann T Pickardt R	1990	Klin Wochenschr1990，68，11：	1
	6	Evolutionary search for difficult problem in-stances to support the design of job shop dispatching rules显示文摘	Branke J Pickardt C W	2011	Europe-an Journal of Operations Research2011，212，1：	1
	7	Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly显示文摘	Alex V. Postma Klaartje van Engelen Judith van de Meerakker Thahira Rahman Susanne Probst Marieke J.H. Baars Ulrike Bauer Thomas Pickardt Silke R. Sperling Felix Berger Antoon F.M. Moorman Barbara J.M. Mulder Ludwig Thierfelder Bernard Keavney Judith Good	2011	Circulation: Cardiovascular Genetics2011，，：	1
	8	A Biobank for Long-term and Sustainable Research in the Field of Congenital Heart Disease in Germany显示文摘Congenital heart disease(CHD) is the most frequent birth defect(0.8%–1% of all live births). Due to the advance in prenatal and postnatal early diagnosis and treatment, more than90% of these patients survive into adulthood today. However, several mid- and long-term morbidities are dominating the follow-up of these patients. Due to the rarity and heterogeneity of the phenotypes of CHD, multicenter registry-based studies are required. The CHD-Biobank was established in 2009 with the aim to collect DNA from patients and their parents(trios) or from affected families, as well as cardiovascular tissues from patients undergoing corrective heart surgery for cardiovascular malformations. Clinical/phenotype data are matched to the International Paediatric and Congenital Cardiac Code(IPCCC) and the International Statistical Classi?cation of Diseases and Related Health Problems 10 th Revision(ICD-10). The DNA collection currently comprises samples from approximately 4200 participants with a wide range of CHD phenotypes.The collection covers about 430 trios and 120 families with more than one affected member. The cardiac tissue collection comprises 1143 tissue samples from 556 patients after open heart surgery.	Thomas Pickardt Eva Niggemeyer Ulrike M.M.Bauer Hashim Abdul-Khaliq Competence Network for Congenital Heart Defects Investigators	2016	Genomics, Proteomics & Bioinformatics2016，14，4：	0

返回顶部每页显示：

共1页首页上一页第1页下一页末页 /1 跳转

goolge学术搜索-维普

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1　渝公网安备 50019002500403号　违法和不良信息举报中心

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费