Schon EA - Search Results

1

Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach.

Tritschler HJ, Bonilla E, Lombes A, Andreetta F, Servidei S, Schneyder B, Miranda AF, Schon EA, Kadenbach B, DiMauro S. Tritschler HJ, et al. Among authors: schon ea. Neurology. 1991 Feb;41(2 ( Pt 1)):300-5. doi: 10.1212/wnl.41.2_part_1.300. Neurology. 1991. PMID: 1846953

2

Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiency.

Tay SK, Nesti C, Mancuso M, Schon EA, Shanske S, Bonilla E, Davidson MM, Dimauro S. Tay SK, et al. Among authors: schon ea. Arch Neurol. 2004 Dec;61(12):1935-7. doi: 10.1001/archneur.61.12.1935. Arch Neurol. 2004. PMID: 15596615

3

The many clinical faces of cytochrome c oxidase deficiency.

DiMauro S, Tanji K, Schon EA. DiMauro S, et al. Among authors: schon ea. Adv Exp Med Biol. 2012;748:341-57. doi: 10.1007/978-1-4614-3573-0_14. Adv Exp Med Biol. 2012. PMID: 22729865 Review.

4

Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease.

Salviati L, Sacconi S, Rasalan MM, Kronn DF, Braun A, Canoll P, Davidson M, Shanske S, Bonilla E, Hays AP, Schon EA, DiMauro S. Salviati L, et al. Among authors: schon ea. Arch Neurol. 2002 May;59(5):862-5. doi: 10.1001/archneur.59.5.862. Arch Neurol. 2002. PMID: 12020273

5

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.

6

Mitochondrial encephalomyopathies: biochemical approach.

Dimauro S, Moraes CT, Shanske S, Lombes A, Nakase H, Mita S, Tritschler HJ, Bonilla E, Miranda AF, Schon EA. Dimauro S, et al. Among authors: schon ea. Rev Neurol (Paris). 1991;147(6-7):443-9. Rev Neurol (Paris). 1991. PMID: 1660180 Review.

7

Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathies.

Andreetta F, Tritschler HJ, Schon EA, DiMauro S, Bonilla E. Andreetta F, et al. Among authors: schon ea. J Neurol Sci. 1991 Sep;105(1):88-92. doi: 10.1016/0022-510x(91)90123-o. J Neurol Sci. 1991. PMID: 1665507 Free article.

8

Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome.

Lombes A, Nakase H, Tritschler HJ, Kadenbach B, Bonilla E, DeVivo DC, Schon EA, DiMauro S. Lombes A, et al. Among authors: schon ea. Neurology. 1991 Apr;41(4):491-8. doi: 10.1212/wnl.41.4.491. Neurology. 1991. PMID: 1849240

9

Cytochrome c oxidase deficiency.

DiMauro S, Lombes A, Nakase H, Mita S, Fabrizi GM, Tritschler HJ, Bonilla E, Miranda AF, DeVivo DC, Schon EA. DiMauro S, et al. Among authors: schon ea. Pediatr Res. 1990 Nov;28(5):536-41. doi: 10.1203/00006450-199011000-00025. Pediatr Res. 1990. PMID: 2175026 Review.

10

Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.

Mita S, Schmidt B, Schon EA, DiMauro S, Bonilla E. Mita S, et al. Among authors: schon ea. Proc Natl Acad Sci U S A. 1989 Dec;86(23):9509-13. doi: 10.1073/pnas.86.23.9509. Proc Natl Acad Sci U S A. 1989. PMID: 2556715 Free PMC article.

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