Schon EA - Search Results

1

Cytochrome oxidase deficiency: clinical and biochemical heterogeneity.

DiMauro S, Zeviani M, Servidei S, Bonilla E, Miranda AF, Prelle A, Schon EA. DiMauro S, et al. Among authors: schon ea. Ann N Y Acad Sci. 1986;488:19-32. doi: 10.1111/j.1749-6632.1986.tb46545.x. Ann N Y Acad Sci. 1986. PMID: 3034115 Review. No abstract available.

2

Clinical and biochemical studies on cytochrome oxidase deficiencies.

Schon EA, Bonilla E, Lombes A, Moraes CT, Nakase H, Rizzuto R, Zeviani M, DiMauro S. Schon EA, et al. Ann N Y Acad Sci. 1988;550:348-59. doi: 10.1111/j.1749-6632.1988.tb35349.x. Ann N Y Acad Sci. 1988. PMID: 2854407 No abstract available.

3

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.

4

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.

5

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

6

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.

7

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.

8

Biochemical and molecular aspects of cytochrome C oxidase deficiency.

DiMauro S, Zeviani M, Servidei S, Prelle A, Miranda AF, Bonilla E, Schon EA. DiMauro S, et al. Among authors: schon ea. Adv Neurol. 1988;48:93-105. Adv Neurol. 1988. PMID: 2825476 Review. No abstract available.

9

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.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

248 results

Search Page