Published in Int J Cardiol on September 25, 2015
An unusual case of left ventricle noncompaction. Int J Cardiol (2015) 1.38
Sudden cardiac death in neuromuscular disorders. Int J Cardiol (2015) 1.49
Effects of antiepileptic drugs on mitochondrial functions, morphology, kinetics, biogenesis, and survival. Epilepsy Res (2017) 1.39
Cardiac manifestations of primary mitochondrial disorders. Int J Cardiol (2014) 1.37
The genetic background of left ventricular hypertrabeculation / noncompaction remains vague. Rev Esp Cardiol (Engl Ed) (2014) 1.10
Is ketogenic diet truly effective in mitochondrial epilepsy? Pediatr Neurol (2014) 1.08
Left ventricular noncompaction associated with a compound heterozygous MYBPC3 mutation. Eur J Med Genet (2014) 1.07
Left ventricular hypertrabeculation/noncompaction in hyperoxaluria. Turk Kardiyol Dern Ars (2015) 1.07
CNS disease triggering Takotsubo stress cardiomyopathy. Int J Cardiol (2014) 1.07
Noncompaction in Fabry's disease. Rev Port Cardiol (2015) 1.06
Triple occurrence of seizure-associated takotsubo syndrome. Int J Cardiol (2016) 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
Myocarditis in myasthenia gravis. Int J Cardiol (2016) 1.06
Increased prevalence of non-compaction. Eur J Intern Med (2013) 1.06
Double trouble progressive external ophthalmoplegia and Huntington's disease. Mol Genet Metab Rep (2016) 0.89
Grant et al. 1926 did not provide the first description of left ventricular hypertrabeculation/noncompaction. Int J Cardiol (2013) 0.85
Oncocytoma and noncompaction in metabolic myopathy. Int J Cardiol (2016) 0.83
Neuromuscular disorders and Takotsubo syndrome. Int J Cardiol (2013) 0.82
Review of Cardiac Disease in Nemaline Myopathy. Pediatr Neurol (2015) 0.81
Leriche-syndrome despite regular sport and non-compaction suggest neuromuscular disease. Int J Cardiol (2015) 0.81
Noncompaction in alleged motor neuron disease suggests myopathy. Int J Cardiol (2014) 0.80
Stroke-like episodes, peri-episodic seizures, and MELAS mutations. Eur J Paediatr Neurol (2016) 0.80
Influence of mitochondrion-toxic agents on the cardiovascular system. Regul Toxicol Pharmacol (2013) 0.79
Cardiomyopathy in neurological disorders. Cardiovasc Pathol (2013) 0.79
Distal myosin heavy chain-7 myopathy due to the novel transition c.5566G>A (p.E1856K) with high interfamilial cardiac variability and putative anticipation. Neuromuscul Disord (2014) 0.77
Therapeutic strategies for mitochondrial disorders. Pediatr Neurol (2014) 0.77
In the heart of MELAS syndrome. Int J Cardiol (2016) 0.76
Left ventricular hypertrabeculation/noncompaction coincidentally found in sporadic inclusion body myositis. Int J Cardiol (2013) 0.76
Abnormalities of Skin and Cutaneous Appendages in Neuromuscular Disorders. Pediatr Neurol (2015) 0.76
Pregnancy and delivery under the MELAS mutation. Mitochondrion (2016) 0.75
Is left ventricular hypertrabeculation/noncompaction in athletes benign? Int J Cardiol (2014) 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
Management of juvenile stroke from noncompaction with muscular dystrophy. Int J Cardiol (2015) 0.75
Novel MYH7 mutation associated with mild myopathy but life-threatening ventricular arrhythmias and noncompaction. Int J Cardiol (2014) 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
More about seizure-triggered Takotsubo syndrome and SUDEP. Seizure (2015) 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 and the neuromuscular connection. Neuromuscul Disord (2016) 0.75
MELAS syndrome due to the m.3291T > C mutation. Mol Genet Metab Rep (2016) 0.75
Mitochondrial neuropathy affects peripheral and cranial nerves and is primary or secondary or both. Neuromuscul Disord (2016) 0.75
Familial noncompaction on cardiac computed tomography. Int J Cardiol (2016) 0.75
Serious assessment of mtDNA variants is a prerequisite to confirm pathogenicity. J Neurol Sci (2017) 0.75
Acute heart failure from noncompaction requiring emergency heart transplantation. Rev Port Cardiol (2016) 0.75
Stress from myasthenic crisis triggers Takotsubo (broken heart) syndrome. Int J Cardiol (2015) 0.75
Fukutin mutations in Fukuyama congenital muscular dystrophy do not cause noncompaction. Int J Cardiol (2016) 0.75
Non-compaction delineates amyotrophic lateral sclerosis from metabolic myopathy. Int J Cardiol (2014) 0.75
Takotsubo in amyotrophic lateral sclerosis. J Neurol Sci (2017) 0.75
Compound heterozygous fukutin mutation-related non-compaction. Int J Cardiol (2017) 0.75
Nitric Oxide Deficiency Triggering Strokelike Episodes. JAMA Neurol (2016) 0.75
Pathogenicity of the LHON variant m.3472T>C is uncertain. J Neurol Sci (2017) 0.75
Collum-caput (COL-CAP) concept for conceptual anterocollis, anterocaput, and forward sagittal shift. J Neurol Sci (2015) 0.75
Familial accumulation of sudden cardiac deaths and the LMNA variant c.868G>A (p.Glu290Lys). Int J Cardiol (2016) 0.75
Accuracy of clinical and electrophysiological criteria for diagnosing amyotrophic lateral sclerosis. Clin Neurophysiol (2016) 0.75
Leigh-like syndrome due to OPA1 mutations. Eur J Paediatr Neurol (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
Why does Leigh syndrome respond to immunotherapy? Mol Genet Metab Rep (2016) 0.75
Management of epilepsy in MERRF syndrome. Seizure (2017) 0.75
Epilepsy in MELAS. Pediatr Neurol (2016) 0.75
MEGDEL Syndrome. Pediatr Neurol (2020) 0.75
The Eye on Mitochondrial Disorders. J Child Neurol (2015) 0.75
Is vatiquinone truly beneficial for Leigh syndrome? Brain Dev (2017) 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
Affection of the frontal lobe in Leigh syndrome due to the m.8993T>G mutation. J Neurol Sci (2016) 0.75
Variants m.13276G>A in the MT-ND5 and m.8241T>G in the MT-CO2 gene are not responsible for maternally inherited diabetes and deafness. J Diabetes Complications (2017) 0.75
Subarachnoid bleeding triggering Takotsubo syndrome. Int J Cardiol (2015) 0.75
Acquired/hidden noncompaction in metabolic encephalopathy with non-convulsive epileptic state. Int J Cardiol (2014) 0.75
Phenotypic spectrum of DARS2 mutations. J Neurol Sci (2017) 0.75
Axonal hyperexcitability due to Schwann cell involvement in chronic progressive external ophthalmoplegia. Clin Neurophysiol (2017) 0.75
Noncompaction and scleroderma. Turk Kardiyol Dern Ars (2016) 0.75
Cerebro-spinal fluid findings in mitochondrial disorders. Mitochondrion (2012) 0.75
Striatal necrosis due to the m.14459G>A mutation. J Neurol Sci (2017) 0.75
Dementia from the ABCD1 mutation c.1415-1416delAG in a female carrier. Gene (2013) 0.75
Regression of left ventricular hypertrabeculation/noncompaction. J Cardiol (2016) 0.75
Motor neuron disease triggering takotsubo syndrome. Int J Cardiol (2016) 0.75
Avoid mitochondrion-toxic antiepileptic drugs in glycine encephalopathy. Brain Dev (2017) 0.75
Primary prophylactic anticoagulation is mandatory if noncompaction is associated with atrial fibrillation or heart failure. Int J Cardiol (2015) 0.75
Metabolic myopathy facilitating the development of Takotsubo syndrome. Int J Cardiol (2016) 0.75
Mitochondrial disorders of the retinal ganglion cells and the optic nerve. Mitochondrion (2017) 0.75
Comment to the manuscript by Bacalhau et al. On "in silico prediction is insufficient to assess pathogenicity of mtDNA variants". Eur J Med Genet (2017) 0.75
Is the Takotsubo syndrome a brain-heart or multiorgan disorder? J Neurol Sci (2017) 0.75