Published in Ophthalmology on July 01, 2016
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CNS-disease affecting the heart: brain-heart disorders. J Neurol Sci (2014) 0.88
Do lesional perfusion abnormalities on arterial spin labeling truly contribute to the diagnosis of Leigh syndrome? Pediatr Radiol (2016) 0.86
Is chronic fatigue syndrome truly associated with haplogroups or mtDNA single nucleotide polymorphisms? J Transl Med (2016) 0.84
Lamin A/C mutations do not cause left ventricular hypertrabeculation/noncompaction. Tex Heart Inst J (2015) 0.75
Transient symmetric T2-hyperintensities of basal ganglia and brainstem not only point to Leigh syndrome. Ann Indian Acad Neurol (2016) 0.75
Detection of the mutation may guide treatment of heart and muscle in Duchenne muscular dystrophy. Int Med Case Rep J (2016) 0.75
Mitochondrial Disorders May Mimic Amyotrophic Lateral Sclerosis at Onset. Sultan Qaboos Univ Med J (2016) 0.75
Cerebral involvement in mitochondrial disorders on imaging. Childs Nerv Syst (2016) 0.75
Pathogenicity of the Homoplasmic m.8701A>G Variant Requires Confirmation. Chin Med J (Engl) (2016) 0.75
Peculiarities of progressive external ophthalmoplegia due to single mitochondrial DNA deletions. J Formos Med Assoc (2016) 0.75
Mitochondrial multiorgan disorder syndrome score generated from definite mitochondrial disorders. Neuropsychiatr Dis Treat (2017) 0.75
Levels of nitric oxide pathway parameters may depend on heteroplasmy rates of the m.3243A>G mutation. Int J Cardiol (2016) 0.75
Prevalence and Outcome of Mitochondrial Epilepsy. Ann Neurol (2016) 0.75
Renal involvement in MELAS. Med Clin (Barc) (2017) 0.75
Phenotypic spectrum of the m.8344A>G mutation. J Neurol (2016) 0.75
Anterocollis and anterocaput. Clin Neurol Neurosurg (2014) 0.75
Death in Pediatric Mitochondrial Disorders. Pediatr Neurol (2017) 0.75
Takotsubo in Miller-Fisher and Guillain Barre syndrome. Am J Emerg Med (2017) 0.75
Spectrum of Movement Disorders in Mitochondrial Disorders. JAMA Neurol (2016) 0.75
Ophthalmologic involvement in Leigh syndrome. Acta Ophthalmol (2016) 0.75