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67篇 您的检索式：作者名="Santorelli"

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	题名	作者	年代	出处	被引量
1	Carotid Artery Intima-media Thickness in Nonalcoholic Fatty Liver Disease显示文摘	Anna Ludovica Fracanzani Larry Burdick Sara Raselli Paola Pedotti Liliana Grigore Gennaro Santorelli Luca Valenti Alessandra Maraschi Alberico Catapano Silvia Fargion	2008	The American Journal of Medicine2008，，1：	5
2	Carotid Artery Intima-media Thickness in Nonalcoholic Fatty Liver Disease显示文摘	Anna Ludovica Fracanzani Larry Burdick Sara Raselli Paola Pedotti Liliana Grigore Gennaro Santorelli Luca Valenti Alessandra Maraschi Alberico Catapano Silvia Fargion	2008	The American Journal of Medicine2008，，1：	2
3	Methylmalonic and Propionie Aciduria显示文摘	Deodato F Boenzi S Santorelli FM	2006	Seminars in Medical Genetics2006，142，2：	1
4	Collapsing glomerulopathy associ ated with inherited mitochondriai injury显示文摘	Barisoni L Diomedi-Camassei F Santorelli F M Caridi G Thomas D B Emma F	2008	Kidney Int2008，74，：	1
5	Collapsing glomerulopathy associated with inherited mitochondrial injury 显示文摘	Barisoni L Diomedi-Camassei F Santorelli FM	2008	Kidney Int2008，74，2：	1
6	Methylmalonic and propionic aciduria显示文摘	Deodato F Boenzi S Santorelli FM	2006	AM J Med Genet C Sem in Med Genet2006，142，2：	1
7	Methylmalonic and propionic aciduria显示文摘	Deodato F Boenzi S Santorelli FM	2006	Am J Med Genet C Semin Med Genet2006，142，2：	1
8	COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement显示文摘	Diomedi-Camassei F Di Giandomenico S Santorelli FM	2007	J Am Soc Nephrol2007，18，10：	1
9	Clinical features associated with the A to G transition at nucleotide 8344 of mtDNA('MERRF' mtation)显示文摘	Silvestri G Ciafaloni E Santorelli FM	1993	Neurology1993，43，：	1
10	Methylmalonic and Propionic Aciduria显示文摘	Deodato F Boenzi S Santorelli FM	2006	Am J Med Genet C Semin2006，142，2：	1
11	Mechanistic role of p38 MAPK in gastric cancer dissemination in a ro- dent model peritoneal metastasis 显示文摘	Graziosi L Mencarelli A Santorelli C	2012	Eur J Pharmacol2012，674，23：	1
12	Multiplemitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients显示文摘	Santorelli FM Sciacco M Tanji K	1996	Ann Neurol1996，39，6：	1
13	Methylmalonic and propionic aciduria显示文摘	Deodato F Boenzi S Santorelli FM	2006	Am J Med Genet C Semin Med Genet2006，142，2：	1
14	Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmet- ric lipomatosis: further evidence of a possible association 显示文摘	Mancuso M Bianchi MC Santorelli FM	1999	J Neurol1999，246，：	1
15	HyperCKemia as the only sign of McArdle's disease in a child显示文摘	Bruno C Bertini E Santorelli FM	2000	J Child Neurol2000，15，：	1
16	Methylmalonic and propionie aciduria显示文摘	Deodato F Boenzi S Santorelli FM	2006	Am J Med Genet C Semin Med Genet2006，142，2：	1
17	Multiple mitochondrial DNA deletions in sporadic inclusion body myositis:a study of 56 patients显示文摘	Sciacco M Tanji K	1996	Ann Neurol1996，39，6：	1
18	Chronic diarrhea associated with the A3243G mtDNA mutation显示文摘	Santorelli FM Villanova M Malandrini A		0，，：	1
19	Methylmalonic andpropionic aciduria显示文摘	Deodato F Boenzi S Santorelli FM	2006	Am J Med Genet C Semin Med Genet2006，142，：	1
20	The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome 显示文摘	Santorelli FM Shanske S Macaya A	1993	Ann Neurol1993，34，6：	1

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