Published in Metab Brain Dis on September 30, 2017
Toxicity of Antiepileptic Drugs to Mitochondria. Handb Exp Pharmacol (2017) 1.20
Noncompaction in mitochondrial trifunctional protein deficiency due to a HADHB mutation. Eur J Pediatr (2015) 1.08
A commentary on homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome. J Hum Genet (2017) 1.07
Consider a Nongenetic Pathogenesis of Noncompaction. Pediatr Cardiol (2015) 1.06
Genetic Counselling for Maternally Inherited Mitochondrial Disorders. Mol Diagn Ther (2017) 0.92
Mitochondrial diabetes in Germany and Austria. Eur J Pediatr (2016) 0.86
Is chronic fatigue syndrome truly associated with haplogroups or mtDNA single nucleotide polymorphisms? J Transl Med (2016) 0.84
Onset Manifestations of Spinal and Bulbar Muscular Atrophy (Kennedy's Disease). J Mol Neurosci (2015) 0.78
Cerebral involvement in mitochondrial disorders on imaging. Childs Nerv Syst (2016) 0.75
Potential causes of sudden cardiac death in nemaline myopathy. Ital J Pediatr (2015) 0.75
Traumatic brain injury is unlikely precipitating Leigh syndrome due to the GJB2 mutation c.35delG. Emerg (Tehran) (2017) 0.75
Erratum to: Genetic Counselling for Maternally Inherited Mitochondrial Disorders. Mol Diagn Ther (2017) 0.75
Phenotypic Heterogeneity of the m.14459G>A Mutation. Child Neurol Open (2017) 0.75
Emergencies in motoneuron disease. Intern Emerg Med (2017) 0.75
Involvement of the cerebral veins in MELAS syndrome? Neuroradiology (2017) 0.75
Correction to: Contribution of the MRPS22 variant and a Down mosaic to the phenotype. Metab Brain Dis (2017) 0.75
Phenotypic and genotypic features in pediatric and adult mitochondrial disorders. Muscle Nerve (2017) 0.75