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Seizure: European Journal of Epilepsy, ISSN 1059-1311, 08/2017, Volume 50, pp. 166 - 170
Journal Article
Expert Opinion on Pharmacotherapy, ISSN 1465-6566, 07/2019, Volume 20, Issue 10, pp. 1289 - 1297
Introduction: Epilepsy is a prominent feature of myoclonic epilepsy with ragged-red fibers (MERRF)-syndrome. The most frequent seizure type is myoclonic... 
epilepsy | antiepileptic drugs | MERRF syndrome | gene | mitochondrial disorder | seizures | m.8344A>G | MYOCLONIC-ASTATIC EPILEPSY | TRANSFER-RNA LYS | PHENOTYPE | MITOCHONDRIAL-DNA | G8363A MUTATION | 8344A>G | MERRF/MELAS OVERLAP SYNDROME | A8344G MUTATION | PHARMACOLOGY & PHARMACY | STROKE-LIKE EPISODES | PATIENT | RAGGED-RED FIBERS
Journal Article
Neurotherapeutics, ISSN 1933-7213, 4/2013, Volume 10, Issue 2, pp. 227 - 242
Journal Article
Epilepsia, ISSN 0013-9580, 09/2012, Volume 53, Issue 4, pp. 81 - 91
Journal Article
Neurology, ISSN 0028-3878, 04/2005, Volume 64, Issue 7, pp. 1204 - 1208
Journal Article
Muscle & Nerve, ISSN 0148-639X, 09/2011, Volume 44, Issue 3, pp. 448 - 451
Journal Article
Journal Article
Journal of Neurology, ISSN 0340-5354, 3/2003, Volume 250, Issue 3, pp. 267 - 277
Mitochondrial cytopathies represent a heterogeneous group of multisystem disorders which preferentially affect the muscle and nervous systems. They are caused... 
lactic acidosis | ragged-red fibres | mtDNA | respiratory chain | mitochondrial cytopathy | Mitochondrial cytopathy | MtDNA | Respiratory chain | Lactic acidosis | Ragged-red fibres | COMPLEX I | RESPIRATORY-CHAIN | SPERM MITOCHONDRIA | CLINICAL NEUROLOGY | CYTOCHROME-C-OXIDASE | MULTIPLE DELETIONS | EXTERNAL OPHTHALMOPLEGIA | HEREDITARY OPTIC NEUROPATHY | PREEXCITATION SYNDROME | RAGGED-RED FIBERS | PRENATAL-DIAGNOSIS | Mitochondrial Myopathies - metabolism | Humans | Ophthalmoplegia - physiopathology | Optic Atrophy, Hereditary, Leber - genetics | Leigh Disease - metabolism | Mitochondrial Myopathies - therapy | MELAS Syndrome - genetics | Kearns-Sayre Syndrome - physiopathology | Kearns-Sayre Syndrome - metabolism | DNA, Mitochondrial - genetics | MERRF Syndrome - genetics | Optic Atrophy, Hereditary, Leber - metabolism | Mitochondrial Myopathies - diagnosis | Optic Atrophy, Hereditary, Leber - physiopathology | Leigh Disease - physiopathology | Kearns-Sayre Syndrome - genetics | MERRF Syndrome - physiopathology | MELAS Syndrome - metabolism | MELAS Syndrome - physiopathology | MERRF Syndrome - metabolism | Mitochondrial Myopathies - physiopathology | Leigh Disease - genetics | Mitochondrial Myopathies - genetics | Animals | Ophthalmoplegia - genetics | Ophthalmoplegia - metabolism | Causes of | Genetic aspects | Mitochondrial DNA | Mitochondrial myopathies | Research
Journal Article
Wiley Interdisciplinary Reviews: RNA, ISSN 1757-7004, 05/2011, Volume 2, Issue 3, pp. 376 - 386
Journal Article
Journal Article
Journal Article
Kidney International, ISSN 0085-2538, 03/2015, Volume 87, Issue 3, pp. 610 - 622
Journal Article