How can we treat mitochondrial encephalomyopathies? Approaches to therapy. [PDF]
Horvath R, Gorman G, Chinnery PF.
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The long road to a rare diagnosis: A Malaysian case of childhood-onset progressive myoclonus, ataxia, and retinal dystrophy with biopsy features suggestive of mitochondrial dysfunction. [PDF]
Yoga Ratnam KK, Yap JF.
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Wernicke Encephalopathy Complicating a Distinctive POLG Phenotype With MNGIE-Like Features. [PDF]
Capece G +13 more
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Progressive Axonal Neuropathy and Cerebellar Ataxia Associated with Homozygous Pathogenic <i>POLG</i> Mutation in a Patient of African Descent from Northern Minas Gerais/Jequitinhonha Valley, Brazil: A Case Report and Epidemiological Implications. [PDF]
Melo CF +2 more
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Glioblastoma in a Patient With MELAS Syndrome: A Case Report. [PDF]
Chang SM +6 more
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Remimazolam-based anesthesia with intraoperative motor evoked potential monitoring in a patient with Leigh syndrome undergoing scoliosis surgery: a case report. [PDF]
Kuwabara T +5 more
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Severe mitochondrial cardiomyopathy with m.3303C > T variant in the mitochondrial tRNA<sup>Leu(UUR)</sup> gene: A study of large family analysis. [PDF]
Yatsuga S.
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The Citric Acid Cycle Modulates Neurologic Health and Is a Therapeutic Target of Dietary and Genetic Modification in Metabolic Disease. [PDF]
Fogle KJ +7 more
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Molecular and Cellular Mechanisms of Epilepsy 2.0. [PDF]
Zaitsev AV.
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