PubRank

Byung Chan Lim

Author PubWeight™ 16.92‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Clinical features of A3243G mitochondrial tRNA mutation. Brain Dev 2004 0.97
2 A case of Rubinstein-Taybi Syndrome with a CREB-binding protein gene mutation. Korean J Pediatr 2010 0.91
3 Cerebellum can be a possible generator of progressive myoclonus. J Child Neurol 2009 0.88
4 A case of mucolipidosis II presenting with prenatal skeletal dysplasia and severe secondary hyperparathyroidism at birth. Korean J Pediatr 2012 0.86
5 Long-term effectiveness of ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy. Brain Dev 2011 0.86
6 Distinct neurological features in a patient with Schinzel-Giedion syndrome caused by a recurrent SETBP1 mutation. Childs Nerv Syst 2013 0.83
7 A case of isodicentric chromosome 15 presented with epilepsy and developmental delay. Korean J Pediatr 2012 0.83
8 Effectiveness of intravenous levetiracetam as an adjunctive treatment in pediatric refractory status epilepticus. Pediatr Emerg Care 2014 0.83
9 Electroencephalography in pediatric moyamoya disease: reappraisal of clinical value. Childs Nerv Syst 2013 0.82
10 Clinical and EEG risk factors for subsequent epilepsy in patients with complex febrile seizures. Epilepsy Res 2013 0.81
11 Paroxysmal nonepileptic events in pediatric patients confirmed by long-term video-EEG monitoring--Single tertiary center review of 143 patients. Epilepsy Behav 2012 0.80
12 Clinical presentations and neurodevelopmental outcomes of perinatal stroke in preterm and term neonates: a case series. J Korean Med Sci 2010 0.79
13 Development of korean rare disease knowledge base. Healthc Inform Res 2012 0.78
14 Magnetoencephalography in pediatric lesional epilepsy surgery. J Korean Med Sci 2012 0.78
15 Outcome evaluation of intravenous infusion of urokinase for acute ischemic stroke. Chonnam Med J 2012 0.78
16 Short-term efficacy and tolerability of rufinamide adjunctive therapy in children with refractory generalised epilepsy. Epileptic Disord 2013 0.77
17 Involuntary movement in pediatric moyamoya disease patients: consideration of pathogenetic mechanism using neuroimaging studies. Childs Nerv Syst 2013 0.76
18 Ischemic stroke in a 7-month-old infant with antiphospholipid antibody and homozygous C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism. J Child Neurol 2010 0.76
19 Subclinical hypothyroidism during valproic acid therapy in children and adolescents with epilepsy. Neuropediatrics 2012 0.76
20 Intraspinal ganglion cyst. Chonnam Med J 2012 0.75
21 A case of Becker muscular dystrophy with early manifestation of cardiomyopathy. Korean J Pediatr 2012 0.75
22 Infantile Pompe disease: clinical and genetic characteristics with an experience of enzyme replacement therapy. J Child Neurol 2011 0.75
23 Low incidence of SCN1A genetic mutation in patients with hemiconvulsion-hemiplegia-epilepsy syndrome. Epilepsy Res 2013 0.75
24 Coexisting seizures in patients with infantile spasms confirmed by long-term video-electroencephalography monitoring. Epilepsy Res 2012 0.75
25 A 13-year-old girl with proximal weakness and hypertrophic cardiomyopathy with Danon disease. Muscle Nerve 2010 0.75
26 Rare coincidence of familial central core disease and hemophagocytic lymphohistiocytosis. Pediatr Int 2014 0.75
27 A single large-scale deletion of mtDNA in a child with recurrent encephalopathy and tubulopathy. J Neurol Sci 2010 0.75
28 Comparison of flunarizine and topiramate for the prophylaxis of pediatric migraines. Eur J Paediatr Neurol 2012 0.75