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Steroids in intractable childhood epilepsy: clinical experience and review of the literature.
Seizure. 2005 Sep;14(6):412-21. doi: 10.1016/j.seizure.2005.07.002.
Seizure. 2005.
PMID: 16087358
Free article.
Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder.
Coughlin CR 2nd, Scharer GH, Friederich MW, Yu HC, Geiger EA, Creadon-Swindell G, Collins AE, Vanlander AV, Coster RV, Powell CA, Swanson MA, Minczuk M, Van Hove JL, Shaikh TH.
Coughlin CR 2nd, et al. Among authors: coster rv.
J Med Genet. 2015 Aug;52(8):532-40. doi: 10.1136/jmedgenet-2015-103049. Epub 2015 Mar 18.
J Med Genet. 2015.
PMID: 25787132
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Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.
Papadopoulou LC, Sue CM, Davidson MM, Tanji K, Nishino I, Sadlock JE, Krishna S, Walker W, Selby J, Glerum DM, Coster RV, Lyon G, Scalais E, Lebel R, Kaplan P, Shanske S, De Vivo DC, Bonilla E, Hirano M, DiMauro S, Schon EA.
Papadopoulou LC, et al. Among authors: coster rv.
Nat Genet. 1999 Nov;23(3):333-7. doi: 10.1038/15513.
Nat Genet. 1999.
PMID: 10545952
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Linezolid-induced inhibition of mitochondrial protein synthesis.
De Vriese AS, Coster RV, Smet J, Seneca S, Lovering A, Van Haute LL, Vanopdenbosch LJ, Martin JJ, Groote CC, Vandecasteele S, Boelaert JR.
De Vriese AS, et al. Among authors: coster rv.
Clin Infect Dis. 2006 Apr 15;42(8):1111-7. doi: 10.1086/501356. Epub 2006 Mar 13.
Clin Infect Dis. 2006.
PMID: 16575728
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Ultrastructural localization of cytochrome c in apoptosis demonstrates mitochondrial heterogeneity.
D'Herde K, De Prest B, Mussche S, Schotte P, Beyaert R, Coster RV, Roels F.
D'Herde K, et al. Among authors: coster rv.
Cell Death Differ. 2000 Apr;7(4):331-7. doi: 10.1038/sj.cdd.4400655.
Cell Death Differ. 2000.
PMID: 10773817
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