Schon EA - Search Results

1

Mitochondrial dysfunction as a mechanism of CNS injury.

DiMauro S, Simonetti S, Chen X, Petruzzella V, Hirano M, Shanske S, Moraes CT, Schon EA. DiMauro S, et al. Among authors: schon ea. Res Publ Assoc Res Nerv Ment Dis. 1993;71:67-79. Res Publ Assoc Res Nerv Ment Dis. 1993. PMID: 8417473 Review. No abstract available.

2

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions.

Moraes CT, Ricci E, Petruzzella V, Shanske S, DiMauro S, Schon EA, Bonilla E. Moraes CT, et al. Among authors: schon ea. Nat Genet. 1992 Aug;1(5):359-67. doi: 10.1038/ng0892-359. Nat Genet. 1992. PMID: 1284549

3

Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA.

Moraes CT, Ciacci F, Silvestri G, Shanske S, Sciacco M, Hirano M, Schon EA, Bonilla E, DiMauro S. Moraes CT, et al. Among authors: schon ea. Neuromuscul Disord. 1993 Jan;3(1):43-50. doi: 10.1016/0960-8966(93)90040-q. Neuromuscul Disord. 1993. PMID: 8392410

4

Mitochondrial DNA and RNA processing in MELAS.

Kaufmann P, Koga Y, Shanske S, Hirano M, DiMauro S, King MP, Schon EA. Kaufmann P, et al. Among authors: schon ea. Ann Neurol. 1996 Aug;40(2):172-80. doi: 10.1002/ana.410400208. Ann Neurol. 1996. PMID: 8773598

5

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.

6

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.

7

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.

8

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.

9

The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.

Moraes CT, Ricci E, Bonilla E, DiMauro S, Schon EA. Moraes CT, et al. Among authors: schon ea. Am J Hum Genet. 1992 May;50(5):934-49. Am J Hum Genet. 1992. PMID: 1315123 Free PMC article.

10

Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease.

Petruzzella V, Chen X, Schon EA. Petruzzella V, et al. Among authors: schon ea. Biochem Biophys Res Commun. 1992 Jul 15;186(1):491-7. doi: 10.1016/s0006-291x(05)80834-4. Biochem Biophys Res Commun. 1992. PMID: 1352971 Free article.

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