Castro-GagoMPérez-GayLEirís-PuñalJ. Dravet syndrome and mitochondrial dysfunction. J Child Neurol. 2011;26:1331-1332.
3.
Castro-GagoMEirisJFernandez-BustilloJ. Severe myoclonic epilepsy associated with mitochondrial cytopathy. Childs Nerv Syst. 1995;11:630–633.
4.
Castro-GagoMMartinon SanchezJMRodriguez-NunezAHerranz FernandezJLEiris-PunalJ. Severe myoclonic epilepsy and mitochondrial cytopathy. Childs Nerv Syst. 1997;13:570–571.
SpecchioNFuscoLClapsDVigevanoF. Epileptic encephalopathy in children possibly related to immune-mediated pathogenesis. Brain Dev. 2010;32:51–56.
10.
RiaziKGalicMAPittmanQJ. Contributions of peripheral inflammation to seizure susceptibility: cytokines and brain excitability. Epilepsy Res. 2010;89:34–42.
11.
WallaceDC. Mitochondrial diseases in man and mouse. Science. 1999;283:1482–1488.
12.
Fernandez-ChecaJCKaplowitzNGarcia-RuizC. GSH transport in mitochondria: defense against TNF-induced oxidative stress and alcohol-induced defect. Am J Physiol. 1997;273:G7–G17.
13.
SamavatiLLeeIMathesILottspeichFHuttemannM. Tumor necrosis factor alpha inhibits oxidative phosphorylation through tyrosine phosphorylation at subunit I of cytochrome C oxidase. J Biol Chem. 2008;283:21134–21144.
14.
VempatiUDDiazFBarrientosA. Role of cytochrome C in apoptosis: increased sensitivity to tumor necrosis factor alpha is associated with respiratory defects but not with lack of cytochrome C release. Mol Cell Biol. 2007;27:1771–1783.
15.
SuematsuNTsutsuiHWenJ. Oxidative stress mediates tumor necrosis factor–alpha-induced mitochondrial DNA damage and dysfunction in cardiac myocytes. Circulation. 2003;107:1418–1423.
16.
SinhaSPatilSAJayalekshmyVSatishchandraP. Do cytokines have any role in epilepsy?. Epilepsy Res. 2008;82:171–176.
17.
LiGBauerSNowakM. Cytokines and epilepsy. Seizure. 2011;20:249–256.
18.
Fernández-JaénALeonMCMartinez-GraneroMA. Diagnosis in severe myoclonic epilepsy in childhood: study of 13 cases. Rev Neurol. 1998;26:759–762.
19.
BolszakMAnttonenAKKomulainenT. Digenic mutations in severe myoclonic epilepsy of infancy. Epilepsy Res. 2009;85:300–304.
20.
ZsurkaGBaronMStewartJD. Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma. J Neuropathol Exp Neurol. 2008;67:857–866.
21.
LorenzoniPJScolaRHKayCS. MERRF: clinical features, muscle biopsy and molecular genetics in Brazilian patients. Mitochondrion. 2011;11:528–532.
22.
RamelliGPGallatiSWeisJKrahenbuhlSBurgunderJM. Point mutation tRNA(Ser(UCN)) in a child with hearing loss and myoclonus epilepsy. J Child Neurol. 2006;21:253–255.
23.
RossignolDAFryeRE. Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis. Mol Psychiatry. 2011Jan25. [Epub ahead of print].
24.
KlopstockTYu-Wai-ManPDimitriadisK. A randomized placebo-controlled trial of idebenone in Leber’s hereditary optic neuropathy. Brain. 2011Jul25. [Epub ahead of print].
