标题
Epilepsy in Leigh Syndrome With Mitochondrial DNA Mutations
作者
关键词
-
出版物
Frontiers in Neurology
Volume 10, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2019-05-08
DOI
10.3389/fneur.2019.00496
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Pediatric epilepsies misdiagnosed as gastrointestinal disorders
- (2018) Giulia Carbonari et al. EPILEPSY & BEHAVIOR
- Instruction manual for the ILAE 2017 operational classification of seizure types
- (2017) Robert S. Fisher et al. EPILEPSIA
- ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy
- (2016) Roberto D’Angelo et al. NEUROLOGICAL SCIENCES
- 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
- The neuroimaging of Leigh syndrome: case series and review of the literature
- (2016) Eliana Bonfante et al. PEDIATRIC RADIOLOGY
- Leigh syndrome: One disorder, more than 75 monogenic causes
- (2015) Nicole J. Lake et al. ANNALS OF NEUROLOGY
- Seizure semiology and EEG findings in mitochondrial diseases
- (2014) Justyna A. Chevallier et al. EPILEPSIA
- Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlations
- (2014) M Bricout et al. JOURNAL OF MEDICAL GENETICS
- A multicenter study on Leigh syndrome: disease course and predictors of survival
- (2014) Kalliopi Sofou et al. Orphanet Journal of Rare Diseases
- Mitochondrial epilepsy in pediatric and adult patients
- (2013) J. Finsterer et al. ACTA NEUROLOGICA SCANDINAVICA
- Unexplained gastrointestinal symptoms: Think mitochondrial disease
- (2013) Thomas P. Chapman et al. DIGESTIVE AND LIVER DISEASE
- High Risk of Gastrointestinal Hemorrhage in Patients With Epilepsy: A Nationwide Cohort Study
- (2013) Chun-Chieh Yeh et al. MAYO CLINIC PROCEEDINGS
- MRI of the brain in childhood-onset mitochondrial disorders with central nervous system involvement
- (2013) Kalliopi Sofou et al. MITOCHONDRION
- L’imagerie par résonance magnétique dans l’exploration des épilepsies de l’enfant
- (2012) M. Trichard et al. ARCHIVES DE PEDIATRIE
- Classical MERRF phenotype associated with mitochondrial tRNALeu (m.3243A>G) mutation
- (2012) Florian Brackmann et al. EUROPEAN JOURNAL OF PEDIATRICS
- Epilepsy in mitochondrial disorders
- (2012) Josef Finsterer et al. SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
- Juvenile Leigh Syndrome, Optic Atrophy, Ataxia, Dystonia, and Epilepsy due to T14487C Mutation in the mtDNA-ND6 Gene: A Mitochondrial Syndrome Presenting From Birth to Adolescence
- (2011) Esther Leshinsky-Silver et al. JOURNAL OF CHILD NEUROLOGY
- Epileptic Seizures in Infants and Children With Mitochondrial Diseases
- (2011) Hsiu-Fen Lee et al. PEDIATRIC NEUROLOGY
- Malnutrition and epilepsy: A two-way relationship
- (2009) Sabrina Crepin et al. CLINICAL NUTRITION
- MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome
- (2008) Karin Naess et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Mitochondrial respiratory chain defects: Underlying etiology in various epileptic conditions
- (2008) Young Mock Lee et al. EPILEPSIA
- Neuroimaging of mitochondrial disease
- (2008) Russell P. Saneto et al. MITOCHONDRION
- Epilepsy and Respiratory Chain Defects in Children with Mitochondrial Encephalopathies
- (2008) D. Khurana et al. NEUROPEDIATRICS
- Leigh and Leigh-Like Syndrome in Children and Adults
- (2008) Josef Finsterer PEDIATRIC NEUROLOGY
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