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32篇 您的检索式：作者名="PISCIOTTA L"

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	题名	作者	年代	出处	被引量
1	Denaturing high-perform- ance liquid chromatography in the detection of ABCA1 gene mutations in familial HDI deficiency显示文摘	Fasano T Bocchi L Pisciotta L	2005	J Lipid Res2005，46，4：	1
2	Lysosomal lipase deficiency:molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease显示文摘	Fasano T Pisciotta L Bocchi L		0，，03：	1
3	The molecular basis of lecithin : cholesterol acyltransferase deficiency syndromes: a com- prehensive study of molecular and biochemical findings in 13 unre- lated Italian families 显示文摘	Calabresi L Pisciotta L Costantin A	2005	Arterioscler Thromb Vasc Biol2005，25，9：	1
4	Denaturing high- performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficieney显示文摘	Fasano T Bocchi L Pisciotta L	2005	J Lipid Res2005，46，4：	1
5	Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease 显示文摘	BOCCHI L PISCIOTTA L FASANO T	2010	Clin Chim Acta In- tern J Clin Chem2010，411，：	1
6	Inherited apolipoprotein A-V deficieney in severe hypertriglyeeridemia显示文摘	Oliva CP Pisciotta L LiVolti G	2005	Arterioscler Thromb Vasc Biol2005，25，2：	1
7	Genetic polymorphisms af- fecting the phenotypic expression of familial hypereholesterolemia 显示文摘	Bertolini S Pisciotta L Di Scala L	2004	Atherosclerosis2004，174，：	1
8	The molecular basis of lecithin: cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families 显示文摘	CALABRESI L PISCIOTTA L COSTANTIN A	2005	Arterioscler Thromb Vase Biol2005，25，9：	1
9	Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia 显示文摘	Bertolini S Pisciotta L Scala LD	2004	Atherosclerosis2004，174，1：	1
10	Combined monogenic bypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes 显示文摘	PISCIOTTA L CALABRESI L LUPATTELLI G	2005	Atherosclerosis2005，182，1：	1
11	A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease显示文摘	Bertolini S Pisciotta L Seri M	2001	Atherosclerosis2001，154，：	1
12	Autosomalrecessive hypercholesterolemia(ARH)and homozygousfamilial hypercholesterolemia(FH):aphenotypic com-parison显示文摘	Pisciotta L Olivab CP Pes GM	2006	Atherosclerosis2006，188，10：	1
13	Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterole 显示文摘	Bertolini S Pisciotta L Di Scala L	2004	Atherosclerosis2004，174，1：	1
14	Inherited apolipoprotein A-V deficiency in severn hypertriglyceridemia 显示文摘	Priore Oliva C Pisciotta L Li Vohi G Sambataro MP Cantafora A Bellocchio A	2005	Arterioscler Thromb Vasc Biol2005，25，2：	1
15	A silent mu-tation of Niemann-Pick Cl-like 1 and apolipoprotein E4modulate cholesterol absorption in primary hyperlipi-demias显示文摘	Lupattelli G Pisciotta L De Vuono S	2013	J Clin Lipidol2013，7，2：	1
16	Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemia显示文摘	Pisciotta L Li Volti G	2005	Arterioscler Thromb Vasc Biol2005，25，2：	1
17	Beta-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia显示文摘	Calandra S Bertolini S Pes GM Deiana L Tarugi P Pisciotta L	2004	Semin Vasc Med2004，4，3：	1
18	Effect of ezefimibe coadministered with statins in genotype-confirmed heterozygous FH patients 显示文摘	Pisciotta L Fasano T Bellocchio A	2007	Atherosclerosis2007，194，2：	1
19	Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia显示文摘	Bertolini S Pisciotta L Scala L D	2004	Atherosclerosis2004，174，1：	1
20	Denaturing high-per-formance liq- uid chromatography in the detection of ABCA1 gene mutational in familial HDL deficiency显示文摘	Fasano T Bocchi L Pisciotta L	2005	J Lipid Res2005，46，4：	1

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