Clinical features of epileptic seizures in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes

Mitochondrial Epilepsy, a Challenge for Neurologists

(2022) Piervito Lopriore et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome

(2021) Sanjiban Chakrabarty et al.   JOURNAL OF NEUROLOGY

A novel nonsense variant in MT-COX3 causes MELAS syndrome

(2021) Wei Wang et al.   NEUROMUSCULAR DISORDERS

Forecasting stroke-like episodes and outcomes in mitochondrial disease

(2021) Yi Shiau Ng et al.   BRAIN

Migratory Rolandic Encephalopathy Caused by the Mitochondrial ND3 Variant

(2021) Kunqian Ji et al.   NEUROLOGY

Epilepsy in adults

(2019) Roland D Thijs et al.   LANCET

Commonalities in epileptogenic processes from different acute brain insults: Do they translate?

(2017) Pavel Klein et al.   EPILEPSIA

An overview of the 2017 ILAE operational classification of seizure types

(2017) Robert S. Fisher   EPILEPSY & BEHAVIOR

Recurrent Alternate-Sided Homonymous Hemianopia Due to Mitochondrial Encephalomyopathy with Lactic Acidosis and Stroke-Like Episodes (MELAS): A Case Report

(2016) Kristen M. Krysko et al.   NEURO-OPHTHALMOLOGY

Epilepsy Characteristics and Clinical Outcome in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS)

(2016) Ha Neul Lee et al.   PEDIATRIC NEUROLOGY

Focal and Generalized Seizures May Occur in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes (MELAS) Patients

(2015) Josef Finsterer et al.   JOURNAL OF CHILD NEUROLOGY

Mitochondrial dysfunction and seizures: the neuronal energy crisis

(2015) Gábor Zsurka et al.   LANCET NEUROLOGY

MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options

(2015) Ayman W. El-Hattab et al.   MOLECULAR GENETICS AND METABOLISM

Phenotypic Analysis of Epilepsy in the Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes–Associated Mitochondrial DNA A3243G Mutation

(2014) Scott T. Demarest et al.   JOURNAL OF CHILD NEUROLOGY

Mitochondrial Calcium Uptake Capacity Modulates Neocortical Excitability

(2013) Basavaraju G Sanganahalli et al.   JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM

AMPK: a nutrient and energy sensor that maintains energy homeostasis

(2012) D. Grahame Hardie et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

MELAS: A nationwide prospective cohort study of 96 patients in Japan

(2011) Shuichi Yatsuga et al.   BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS

Mitochondrial dysfunction in epilepsy

(2011) Jaroslava Folbergrová et al.   MITOCHONDRION

Epileptic Seizures in Infants and Children With Mitochondrial Diseases

(2011) Hsiu-Fen Lee et al.   PEDIATRIC NEUROLOGY

Mitochondrial Energetics and Therapeutics

(2010) Douglas C. Wallace et al.   Annual Review of Pathology-Mechanisms of Disease

Definition of drug resistant epilepsy: Consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies

(2009) Patrick Kwan et al.   EPILEPSIA

Mitochondrial involvement in temporal lobe epilepsy

(2009) Alexei P. Kudin et al.   EXPERIMENTAL NEUROLOGY

Manifestations of the mitochondrial A3243G mutation

(2008) Josef Finsterer   INTERNATIONAL JOURNAL OF CARDIOLOGY