维普期刊资源整合服务平台（V6.5）

30篇 您的检索式：作者名="Leren TP"

选中清除导出查看参考文献查看引证文献引用追踪共2页首页上一页第1页下一页末页 /2 跳转

	题名	作者	年代	出处	被引量
1	Mutations in the PCSK9 gene in Norwegian sub- jects with autosomal dominant hypercholesterolemia显示文摘	Leren TP	2004	Clin Genet2004，65，5：	1
2	Jervell and Lange-Nielsen syndrome in Norwegian children: aspects around cochlear implantation, hearing, and balance显示文摘	Siem G Friih A Leren TP	2008	Ear Hear2008，29，2：	1
3	Pregnacy outcomes in familial hypercholesterolemia: a registry - based study 显示文摘	Toleikyte I Retterstl K Leren TP	2011	Circulation2011，124，15：	1
4	The unique role of proprotein convertase subtilisin/kexin 9 in cholesterol homeostasis显示文摘	Mousavi SA Berge KE Leren TP	2009	J Intern Med2009，266，6：	1
5	Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia 显示文摘	Leren TP	2004	Cliff Genet2004，65，5：	1
6	Multiple dysfunctions of two apolip oprotein A-I (R160L) also and apoA-I (P165R), that are associated with hypoalphali poproteinemia in heterozy- gous carriers显示文摘	Daum U Leren TP Langer C	1999	J Lipid Res1999，40，3：	1
7	Mutations in the pcsk9 gene in Norwegian subjects with automal dominant hypercholesterolemia显示文摘	Leren TP	2004	Clin Genet2004，65，5：	1
8	Molecular genetics of familial hypercholexterolaemia in Norway显示文摘	Leren TP	1997	J Intern Med1997，241，：	1
9	Missense Mutations in the PCSK9 gene are associated with hypocholesterolemia and possibly increased response to statin therapy 显示文摘	Berge KE Ose L Leren TP	2006	Arterioscler Thromb Vasc Biol2006，10，：	1
10	New SCN5A mutation in a SUDEP victim with idiopathic epilepsy显示文摘	Aurlien D Leren TP		0，，02：	1
11	Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia 显示文摘	Leren TP	2004	Clin Genet2004，65，：	1
12	Heterozygosity for apolipoprotein AI oslo is associated with low levels of high density lipoproten cholesterol and HDL-subclass LpAI/AII but normal levels of HDL-subclass Lp AI显示文摘	Leren TP Bakken KS Daum U	1997	J Lipid Res1997，38，：	1
13	Multiple dysfunctions of two apolip oprotein A-I (R160L) also and apoA-I (P165R), that are associated with hypoalp halipoproteinemia in heterozygous carriers 显示文摘	Leren TP Langer C	1999	J Lipid Res1999，40，3：	1
14	A novel BMPR2 gene mutation associated with exercise-induced pulmonary hypertension in septal defects 显示文摘	Moller T Leren TP Eiklid KL	2010	Scand Cardiovasc J2010，44，6：	1
15	New SCN5A mutation in a SUDEP victim with idiopathic epilepsy显示文摘	Aurlien D Leren TP Tauhell E	2009	Seizure2009，，2：	1
16	A functional polymorphism in the promoter region of the microsomal triglyceride transfer protein ( MTP -493G/T) influences lipoprotein phenotype in familial hypercholesterolemia 显示文摘	Lundahl B Leren TP Ose L	2000	Arterioecler Thromb Vase Biol2000，20，7：	1
17	Heterozygosity for apolipoprotein A-I(R160L)Oslo is associated with low levels of high density lipoprotein cholesterol and HDL-subclass LpA-Ⅰ/A-Ⅱ but normal levels of HDL-subclass LpA-Ⅰ显示文摘	Leren TP Bakken KS Daum U	1997	J Lipid Ras1997，38，1：	1
18	Commentary PCSK9 variants: A new database 显示文摘	Leigha SE Leren TP Humphries SE	2009	Atherosclerosis2009，203，1：	1
19	Diagnosis of familial hypercholesterolemia in general practice using clinical diagnostic criteria or genetic testing as part of cascade genetic screening 显示文摘	Leren TP Finborud TH Manshaus TE	2008	Community Genet2008，11，1：	1
20	Sorting an LDL receptor with bound PCSK9 to intracellular degradation显示文摘	Leren TP	2014	Atherosclerosis2014，237，1：	1

返回顶部每页显示：

共2页首页上一页第1页下一页末页 /2 跳转

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

用户提示