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Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2Treatment of mitochondrial disorders.Use of the Ketogenic Diet to Treat Intractable Epilepsy in Mitochondrial DisordersMitochondrial encephalopathy, lactic acidosis, and stroke-like episode syndrome presenting with prolonged visual aura.Autism and intellectual disability associated with mitochondrial disease and hyperlactacidemia.Mitochondrial disease: genetics and management.Epilepsy in adults with mitochondrial disease: A cohort study.Neuromuscular and systemic presentations in adults: diagnoses beyond MERRF and MELASGenetic forms of epilepsies and other paroxysmal disordersA typical case of myoclonic epilepsy with ragged red fibers (MERRF) and the lessons learned.Novel Vitamin K analogs suppress seizures in zebrafish and mouse models of epilepsy.Mechanisms of epileptogenesis in pediatric epileptic syndromes: Rasmussen encephalitis, infantile spasms, and febrile infection-related epilepsy syndrome (FIRES).Review: Central nervous system involvement in mitochondrial diseaseNutritional and Bioenergetic Considerations in Critically Ill Patients with Acute Neurological Injury.Fast mitochondrial DNA isolation from mammalian cells for next-generation sequencing.Seizures and risk of epilepsy in autoimmune and other inflammatory encephalitis.Understanding the Epilepsy in POLG Related DiseaseMitochondrial hepatopathies: advances in genetics, therapeutic approaches, and outcomes.Mitochondrial disease heterogeneity: a prognostic challenge.Myoclonic epilepsy with ragged-red fibers: A case report.Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.Bayesian network and mechanistic hierarchical structure modeling of increased likelihood of developing intractable childhood epilepsy from the combined effect of mtDNA variants, oxidative damage, and copy number.Anticonvulsant Medications in Mitochondrial Disease.MELAS syndrome diagnosed in ICU in a 56-year-old patient presenting with status epilepticus.A Mitochondrial Disorder in a Middle Age Iranian Patient: Report of a Rare Case.Recent perspectives of pediatric mitochondrial diseases.The spectrum of epilepsy caused by POLG mutations.Movement disorders in mitochondrial disease.Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Mitochondrial diseases and epilepsy.
@en
type
label
Mitochondrial diseases and epilepsy.
@en
prefLabel
Mitochondrial diseases and epilepsy.
@en
P2860
P1433
P1476
Mitochondrial diseases and epilepsy.
@en
P2093
Bernt A Engelsen
P2860
P356
10.1111/J.1528-1167.2012.03618.X
P478
53 Suppl 4
P577
2012-09-01T00:00:00Z