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49篇 您的检索式:作者名="Zeviani M"
    题名 作者 年代 出处 被引量
1Disorder of nuclear mitochondrial intergenomie communication 显示文摘Spinazzola A Zeviani M 2007Biosci Rep2007,27,:1
2Mitochondrial myopathies显示文摘DiMauro S Bonilla E Zeviani M 1985Ann Neurol1985,17,6:1
3Maternally inherited myopathy and car- diomyopathy: association with mutation in mltochondrial DNA tRNALu (UUR) 显示文摘Zeviani M Gellera C Antozzi C 1991Lancet1991,338,8760:1
4Disorders from perturbations of nuclearmitochondrial intergenomic cross-talk显示文摘Spinazzola A Zeviani M 2009J Intern Med2009,265,2:1
5Mitochondrial disorders 显示文摘Zeviani M 2004Suppl Clin Neurophysiol2004,57,:1
6Mitochondrial disorders显示文摘Zeviani M Antozzi C 1997Mol Hum Reprod1997,3,2:1
7Deletions of mitochomdial DNA in Kearns-Sayre Syndrome显示文摘Zeviani M Moraes CT DiMauro S 1988Neurology1988,38,:1
8Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome C oxidase deficiency 显示文摘Pequignot MO Dey R Zeviani M 2001Hum Mutat2001,17,5:1
9Mitochondrial disorders显示文摘Zeviani M Carelli V 0,,05:1
10Mitochondrial medicine:a metabolic perspective on the pathology of oxidative phosphorylation disorders显示文摘Smeitink JA Zeviani M Turnbull DM 2006Cell Metab2006,3,1:1
11Deletions of mitochondrial DNA in Kearns-Sayre syndrome 显示文摘 Moraes CT Dimauro S 1988Neurology1988,38,9:1
12Dominanty,inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA:clinical,morphologic,and biochemical studies显示文摘Servidci S Zeviani M Manfiedi G 1991Neurology1991,41,:1
13Neurological presentations of mitochondrial diseases显示文摘Zeviani M Bertagnolio B Uziel G 1996J Inherit Metab Dis1996,19,:1
14Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome显示文摘Moraes CT DiMauro S Zeviani M 1989New Engl J Mes1989,320,:1
15Altered sulfide (H2S) metabolism in ethylmalonie encephalopathy显示文摘Tiranti V Zeviani M 2013Cold Spring Harb Perspect Biol2013,5,1:1
16Infantile mitochondrialencephalopathy显示文摘Uziel G Ghezzi D Zeviani M 2011Semin Fetal Neonatal Med2011,16,4:1
17Proteome adap- tations in Ethel-deficient mice indicate a role in lipid catabo- lism and cytoskeleton organization via post-translational pro- tein modifications显示文摘Hildebrandt T M Di Meo I Zeviani M 2013Biosci Rep2013,33,4:1
18Mitoehondrial Disorders 显示文摘Zeviani M Di Donato S 2004Brain2004,127,12:1
19Assembly of the oxi- dative phosphorylation system in humans: what we have learned by studying its defects显示文摘Fem6ndez-Vizarra E Tiranti V Zeviani M 2009Biochim Biophys Acta2009,1793,1:1
20Deletions of mitochondria DNA in Keams-Sayre syndrome显示文摘Zeviani M Moraes CT Di Mauro S Nakase H Bonilla E Schon EA 1988Neurology1988,38,9:1
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