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22篇 您的检索式：作者名="SACCONI L"

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	题名	作者	年代	出处	被引量
1	A functionally dominant mitochondrial DNA mutation显示文摘	Sacconi S Salviati L Nishigaki Y	2008	Hum Mol Genet2008，17，：	1
2	Multiphoton muhifocal microscopy exploiting a diffractive optical element 显示文摘	SACCONI L FRONTER E ANTOLINI R	2003	OptLett2003，28，20：	1
3	A novel CRYAB mutation resulting in muhisystemic disease 显示文摘	Sacconi S Fasson L Antoine JC	2012	Neuromuscul Disord2012，22，：	1
4	Optical recording of fast neuronal membrane potential transients in acute mammalian brain slices by second-harmonic generation microscopy显示文摘	Dombeck D A Sacconi L Blanchard-Desce M	2005	Neurophysiol2005，94，：	1
5	Novel SURF1 mutation in a child with subacute encephalopathy and without the radiological features of Leigh syndrome显示文摘	Salviati L Freehauf C Sacconi S		0，，02：	1
6	Fundus autofluorescence changes after ranibizumab treatment for subfoveal choroidal neovascularization sec- ondary to pathologic myopia显示文摘	PARODI MB IACONO P SACCONI R IULIANO L BANDEL- LO F	2015	Am J Ophthalmol2015，160，2：	1
7	A novel CRYAB mutation resulting in multisystemic disease 显示文摘	Sacconi S Feasson L Antoine JC	2012	Neuromuscul Disord2012，22，1：	1
8	Mutation screening in patients with isolated cytochrome c oxidase deficiency显示文摘	Sacconi S Salviati L Sue CM	2003	Pediatr Res2003，53，2：	1
9	A novel CRYAB mutation resulting in muhisystemic disease 显示文摘	Sacconi S F6asson L Antoine JC	2012	Neuromuscul Disord2012，22，：	1
10	A novel CRY- AB mutation resulting in multisystemic disease显示文摘	SACCONI S FEASSON L ANTOINE J C	2012	Neuromuscul Disord2012，22，1：	1
11	Mitochondrial DNA depletion and dGK gene mutations显示文摘	Salviati L Sacconi S Mancuso M	2002	Ann Neurol2002，52，3：	1
12	Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXRIP) in facioscapulohumeral muscular dystrophy patients 显示文摘	DAVIOVIC L SACCONI S BECHARA E G	2008	J Med Genet2008，45，10：	1
13	Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease显示文摘	Salviati L Sacconi S Rasalan MM	2002	Arch Neurol2002，59，5：	1
14	A novel CRYAB mutation resulting in multisystemic disease 显示文摘	Sacconi S Feasson L Antoine JC Pecheux C Bernard R Cobo AM	2012	Neuromuscul Disord2012，22，1：	1
15	Coenzyme QI0 is fre- quently reduced in muscle of patients with mitochondrial myopa- thy显示文摘	Sacconi S Trevisson E Salviati L	2010	Neuromuscul Disord2010，20，1：	1
16	Infantile encephalomyopathy and nephropathy with CoQ10 deficiency :a CoQ10-responsive condi- tion显示文摘	Salviati L Sacconi S Murer L	2005	Neurology2005，65，：	1
17	A Social Contract Account for CSR as an Extended Model of Corporate Governance (II) : Compliance, Reputa- tion and Reciprocity显示文摘	Sacconi L	2007	Journal of Business Ethics2007，，75：	1
18	Four-, five and six-coordinated nickel (Ⅱ) and cobalt(Ⅱ) complexes of Schiff bases derived from pyridine-2-carboxaldehyde and N,N-substituted ethylenediamines 显示文摘	Zakrzewski G Sacconi L	1968	Inorg Chem1968，7，：	1
19	In vivo single branch axotomy induces GAP-43-dependent sprouting and synaptic remodeling in cerebellar cortex显示文摘	Alleqra Mascaro A L Cesare P Sacconi L		0，，：	1
20	High-spin Five-Coordinated 3d Metal Complexes with Pentadentate Schiff Bases 显示文摘	Sacconi L Bertini I	1966	J Am Chem Soc1966，88，：	1

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