Schon EA - Search Results

1

Mitochondrial DNA mutations and pathogenesis.

Schon EA, Bonilla E, DiMauro S. Schon EA, et al. J Bioenerg Biomembr. 1997 Apr;29(2):131-49. doi: 10.1023/a:1022685929755. J Bioenerg Biomembr. 1997. PMID: 9239539 Review.

2

Mitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects.

DiMauro S, Tanji K, Bonilla E, Pallotti F, Schon EA. DiMauro S, et al. Among authors: schon ea. Muscle Nerve. 2002 Nov;26(5):597-607. doi: 10.1002/mus.10194. Muscle Nerve. 2002. PMID: 12402281 Review.

3

Mitochondrial respiratory-chain diseases.

DiMauro S, Schon EA. DiMauro S, et al. Among authors: schon ea. N Engl J Med. 2003 Jun 26;348(26):2656-68. doi: 10.1056/NEJMra022567. N Engl J Med. 2003. PMID: 12826641 Review. No abstract available.

4

Medicinal and genetic approaches to the treatment of mitochondrial disease.

Schon EA, DiMauro S. Schon EA, et al. Curr Med Chem. 2003 Dec;10(23):2523-33. doi: 10.2174/0929867033456503. Curr Med Chem. 2003. PMID: 14529468 Review.

5

Mitochondrial mutations: genotype to phenotype.

Schon EA, DiMauro S. Schon EA, et al. Novartis Found Symp. 2007;287:214-25; discussion 226-33. doi: 10.1002/9780470725207.ch15. Novartis Found Symp. 2007. PMID: 18074641 Review.

6

Mitochondrial disorders in the nervous system.

DiMauro S, Schon EA. DiMauro S, et al. Among authors: schon ea. Annu Rev Neurosci. 2008;31:91-123. doi: 10.1146/annurev.neuro.30.051606.094302. Annu Rev Neurosci. 2008. PMID: 18333761 Review.

7

Human mitochondrial DNA: roles of inherited and somatic mutations.

Schon EA, DiMauro S, Hirano M. Schon EA, et al. Nat Rev Genet. 2012 Dec;13(12):878-90. doi: 10.1038/nrg3275. Nat Rev Genet. 2012. PMID: 23154810 Free PMC article. Review.

8

Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.

Giordano C, Pallotti F, Walker WF, Checcarelli N, Musumeci O, Santorelli F, d'Amati G, Schon EA, DiMauro S, Hirano M, Davidson MM. Giordano C, et al. Among authors: schon ea. Biochem Biophys Res Commun. 2002 Apr 26;293(1):521-9. doi: 10.1016/S0006-291X(02)00256-5. Biochem Biophys Res Commun. 2002. PMID: 12054632

9

Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome.

Shanske S, Tang Y, Hirano M, Nishigaki Y, Tanji K, Bonilla E, Sue C, Krishna S, Carlo JR, Willner J, Schon EA, DiMauro S. Shanske S, et al. Among authors: schon ea. Am J Hum Genet. 2002 Sep;71(3):679-83. doi: 10.1086/342482. Epub 2002 Jul 31. Am J Hum Genet. 2002. PMID: 12152148 Free PMC article.

10

Molecular defects in cytochrome oxidase in mitochondrial diseases.

DiMauro S, Zeviani M, Rizzuto R, Lombes A, Nakase H, Bonilla E, Miranda A, Schon E. DiMauro S, et al. J Bioenerg Biomembr. 1988 Jun;20(3):353-64. doi: 10.1007/BF00769637. J Bioenerg Biomembr. 1988. PMID: 2841309 Review.

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