Published in Mol Genet Metab Rep on April 19, 2016
Reply to: Double trouble progressive external ophthalmoplegia and Huntington's disease. Mol Genet Metab Rep (2016) 0.75
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Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation. Acta Ophthalmol Scand (1998) 1.14
A novel mitochondrial tRNA(Ala) gene variant causes chronic progressive external ophthalmoplegia in a patient with Huntington disease. Mol Genet Metab Rep (2016) 0.95
Executive and visuospatial deficits in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome. Brain (2003) 0.91
A novel mutation (8342G-->A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonus. Neuromuscul Disord (1999) 0.87
[Leigh disease in a 17-year-old boy]. Wiad Lek (1991) 0.84
[A case of MELAS presenting juvenile-onset hyperglycemic chorea-ballism]. Rinsho Shinkeigaku (2005) 0.83
Sensorineural hearing loss in patients with chronic progressive external ophthalmoplegia or Kearns-Sayre syndrome. J Neurol (2005) 0.82
Chronic progressive external ophthalmoplegia with T9957C mitochondrial DNA mutation in a Taiwanese patient. Acta Neurol Taiwan (2011) 0.82
mtDNA nt3243 mutation, external ophthalmoplegia, and hypogonadism in an adolescent girl. Pediatr Neurol (1998) 0.82
Left ventricular hypertrabeculation/noncompaction in hyperoxaluria. Turk Kardiyol Dern Ars (2015) 1.07
Noncompaction in Fabry's disease. Rev Port Cardiol (2015) 1.06
Letter to the Editor: Do not only ablate but also look for myocardial fibrosis and myopathy in noncompaction. Turk Kardiyol Dern Ars (2015) 1.06
In the heart of MELAS syndrome. Int J Cardiol (2016) 0.76
MELAS syndrome due to the m.3291T > C mutation. Mol Genet Metab Rep (2016) 0.75
Mitochondrial vasculopathy due to the m.3243A > G mutation is not restricted to the carotid artery. Mol Genet Metab Rep (2016) 0.75
Assessment of the phenotype genotype variability and correlation in m.3243A > G mutation carriers requires prospective studies. Mol Genet Metab Rep (2016) 0.75
Arrhythmias in MELAS syndrome. Mol Genet Metab Rep (2016) 0.75
Nephrocalcinosis and retinal dystrophy, rare manifestations of MPV17-related mitochondrial depletion syndrome? Mol Genet Metab Rep (2016) 0.75
Leber's hereditary optic neuropathy is multiorgan not mono-organ. Clin Ophthalmol (2016) 0.75
Unusual recovery of respiratory chain complex-III deficiency upon G-tube feeding and a cocktail. Mol Genet Metab Rep (2016) 0.75
Noncompaction with valve abnormalities is rarely associated with neurologic or genetic disease. Int J Cardiol (2015) 0.75
Differentiating acute ischemic lesions from mitochondrial stroke-like lesions on 3D pseudo-continuous arterial spin labelling. J Magn Reson Imaging (2016) 0.75
Nitric Oxide Deficiency Triggering Strokelike Episodes. JAMA Neurol (2016) 0.75
Fukutin mutations in Fukuyama congenital muscular dystrophy do not cause noncompaction. Int J Cardiol (2016) 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
Why does Leigh syndrome respond to immunotherapy? Mol Genet Metab Rep (2016) 0.75
Noncompaction and scleroderma. Turk Kardiyol Dern Ars (2016) 0.75
Epilepsy in MELAS. Pediatr Neurol (2016) 0.75
Rhabdomyolysis in MELAS may be multifactorial. Rinsho Shinkeigaku (2017) 0.75
Mitochondrial neuropathy affects peripheral and cranial nerves and is primary or secondary or both. Neuromuscul Disord (2016) 0.75
The Eye on Mitochondrial Disorders. J Child Neurol (2015) 0.75
Affection of the frontal lobe in Leigh syndrome due to the m.8993T>G mutation. J Neurol Sci (2016) 0.75
Acute heart failure from noncompaction requiring emergency heart transplantation. Rev Port Cardiol (2016) 0.75