Published in J Child Neurol on December 07, 2011
Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations. Nat Genet (2004) 2.82
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2. Brain (2006) 2.77
Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype correlation. Ann Neurol (2002) 1.39
Mitochondrial cardiomyopathy: pathophysiology, diagnosis, and management. Tex Heart Inst J (2013) 1.30
Rapamycin reduces seizure frequency in tuberous sclerosis complex. J Child Neurol (2009) 1.22
Regression of subependymal giant cell astrocytoma with rapamycin in tuberous sclerosis complex. J Child Neurol (2008) 1.02
Subependymal giant cell astrocytoma: diagnosis, screening, and treatment. Recommendations from the International Tuberous Sclerosis Complex Consensus Conference 2012. Pediatr Neurol (2013) 0.99
POLG DNA testing as an emerging standard of care before instituting valproic acid therapy for pediatric seizure disorders. Seizure (2010) 0.98
Incidence of papilledema and obesity in children diagnosed with idiopathic ''benign'' intracranial hypertension: case series and review. J Child Neurol (2010) 0.96
Diffusion tensor tractography of the human brain cortico-ponto-cerebellar pathways: a quantitative preliminary study. J Magn Reson Imaging (2010) 0.94
Diffusion tensor tractography of the somatosensory system in the human brainstem: initial findings using high isotropic spatial resolution at 3.0 T. Eur Radiol (2009) 0.93
Practice patterns of mitochondrial disease physicians in North America. Part 2: treatment, care and management. Mitochondrion (2013) 0.88
Neurologic complications associated with respiratory syncytial virus. Pediatr Neurol (2005) 0.86
Secondary erythromelalgia successfully treated with intravenous immunoglobulin. J Child Neurol (2011) 0.83
Angiostrongylus cantonensis Meningitis and Myelitis, Texas, USA. Emerg Infect Dis (2017) 0.82
FIRST: a practical approach to the causes and management of febrile seizures. J Child Neurol (2008) 0.81
Impaired gastric emptying and small bowel transit in children with mitochondrial disorders. J Pediatr Gastroenterol Nutr (2012) 0.81
Juvenile onset central nervous system folate deficiency and rheumatoid arthritis. J Child Neurol (2007) 0.80
Seizure semiology and EEG findings in mitochondrial diseases. Epilepsia (2014) 0.78
Language dysfunction in epileptic conditions. Semin Pediatr Neurol (2002) 0.78
When epilepsy interferes with word comprehension: findings in Landau-Kleffner syndrome. J Child Neurol (2008) 0.77
Oculomotor executive function abnormalities with increased tic severity in Tourette syndrome. J Child Psychol Psychiatry (2014) 0.77
Severe narrowing of left cavernous carotid artery associated with Fusobacterium necrophorum infection. Anaerobe (2013) 0.77
Adult-onset cerebral folate deficiency. Arch Neurol (2012) 0.76
Heart, brain, and mind: a case series of multifactorial ischemic strokes in children. J Child Neurol (2005) 0.75
Decreased exhaled nitric oxide levels in patients with mitochondrial disorders. Open Respir Med J (2013) 0.75
Poliomyelitis-like syndrome in a child with West Nile virus infection. Pediatr Infect Dis J (2004) 0.75
Trigeminal myokymia in a young girl. J Child Neurol (2003) 0.75
Friedreich-like ataxia as an initial manifestation of mitochondrial DNA 8344A>G mutation. J Child Neurol (2012) 0.75
Lumbar spinal stenosis causing congenital clubfoot. J Child Neurol (2002) 0.75
Transient tonic upgaze deviation: a neuro-ophthalmological complication of acute cerebellitis. J Child Neurol (2012) 0.75
Self-reported reproductive health in women with tuberous sclerosis complex. Genet Med (2013) 0.75