|
1
|
Leukodystrophy in children: a pictorial review of MR imaging features.
|
Radiographics
|
2002
|
1.99
|
|
2
|
Pediatric moyamoya disease: An analysis of 410 consecutive cases.
|
Ann Neurol
|
2010
|
1.22
|
|
3
|
Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform.
|
J Med Genet
|
2011
|
1.14
|
|
4
|
Headache in pediatric moyamoya disease: review of 204 consecutive cases.
|
J Neurosurg
|
2005
|
1.12
|
|
5
|
Longitudinal analyses of the surgical outcomes of pediatric epilepsy patients with focal cortical dysplasia.
|
J Neurosurg Pediatr
|
2010
|
1.06
|
|
6
|
New antiepileptic drugs in pediatric epilepsy.
|
Brain Dev
|
2008
|
1.04
|
|
7
|
Mutations in ND subunits of complex I are an important genetic cause of childhood mitochondrial encephalopathies.
|
J Child Neurol
|
2009
|
1.00
|
|
8
|
Clinical features of A3243G mitochondrial tRNA mutation.
|
Brain Dev
|
2004
|
0.97
|
|
9
|
Surgical outcome of epilepsy caused by cortical dysplasia.
|
Epilepsia
|
2005
|
0.92
|
|
10
|
Epilepsy surgery in children: outcomes and complications.
|
J Neurosurg Pediatr
|
2008
|
0.92
|
|
11
|
A case of Rubinstein-Taybi Syndrome with a CREB-binding protein gene mutation.
|
Korean J Pediatr
|
2010
|
0.91
|
|
12
|
Mutation analysis of MECP2 and clinical characterization in Korean patients with Rett syndrome.
|
J Child Neurol
|
2002
|
0.91
|
|
13
|
Childhood ocular myasthenia gravis.
|
Ophthalmology
|
2003
|
0.90
|
|
14
|
Diagnostic performance of 18F-FDG PET and ictal 99mTc-HMPAO SPET in pediatric temporal lobe epilepsy: quantitative analysis by statistical parametric mapping, statistical probabilistic anatomical map, and subtraction ictal SPET.
|
Seizure
|
2005
|
0.89
|
|
15
|
Cerebellum can be a possible generator of progressive myoclonus.
|
J Child Neurol
|
2009
|
0.88
|
|
16
|
Long-term effectiveness of ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy.
|
Brain Dev
|
2011
|
0.86
|
|
17
|
Merosin-deficient congenital muscular dystrophy in Korea.
|
Brain Dev
|
2008
|
0.86
|
|
18
|
A novel ND3 mitochondrial DNA mutation in three Korean children with basal ganglia lesions and complex I deficiency.
|
Pediatr Res
|
2007
|
0.86
|
|
19
|
Relapsing demyelinating CNS disease in a Korean pediatric population: multiple sclerosis versus neuromyelitis optica.
|
Mult Scler
|
2010
|
0.84
|
|
20
|
A case of isodicentric chromosome 15 presented with epilepsy and developmental delay.
|
Korean J Pediatr
|
2012
|
0.83
|
|
21
|
Distinct neurological features in a patient with Schinzel-Giedion syndrome caused by a recurrent SETBP1 mutation.
|
Childs Nerv Syst
|
2013
|
0.83
|
|
22
|
Effectiveness of intravenous levetiracetam as an adjunctive treatment in pediatric refractory status epilepticus.
|
Pediatr Emerg Care
|
2014
|
0.83
|
|
23
|
De novo interstitial deletion of 3q22.3-q25.2 encompassing FOXL2, ATR, ZIC1, and ZIC4 in a patient with blepharophimosis/ptosis/epicanthus inversus syndrome, Dandy-Walker malformation, and global developmental delay.
|
J Child Neurol
|
2011
|
0.83
|
|
24
|
Familial occurrence of moyamoya disease: a clinical study.
|
Childs Nerv Syst
|
2006
|
0.82
|
|
25
|
Electroencephalography in pediatric moyamoya disease: reappraisal of clinical value.
|
Childs Nerv Syst
|
2013
|
0.82
|
|
26
|
Fukutin mutations in congenital muscular dystrophies with defective glycosylation of dystroglycan in Korea.
|
Neuromuscul Disord
|
2010
|
0.82
|
|
27
|
Clinical and EEG risk factors for subsequent epilepsy in patients with complex febrile seizures.
|
Epilepsy Res
|
2013
|
0.81
|
|
28
|
Characteristics of patients with epilepsy who use a website providing healthcare information about epilepsy in South Korea.
|
Epilepsy Behav
|
2012
|
0.81
|
|
29
|
SCN1A mutational analysis in Korean patients with Dravet syndrome.
|
Seizure
|
2011
|
0.81
|
|
30
|
Surgical outcome and prognostic factors of pediatric epilepsy caused by cortical dysplasia.
|
Childs Nerv Syst
|
2006
|
0.80
|
|
31
|
Influence of MECP2 gene mutation and X-chromosome inactivation on the Rett syndrome phenotype.
|
J Child Neurol
|
2004
|
0.80
|
|
32
|
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
|
|
33
|
Molecular diagnosis of congenital muscular dystrophies with defective glycosylation of alpha-dystroglycan using next-generation sequencing technology.
|
Neuromuscul Disord
|
2013
|
0.78
|
|
34
|
Biochemical and genetic analysis of Leigh syndrome patients in Korea.
|
Brain Dev
|
2007
|
0.78
|
|
35
|
Magnetoencephalography in pediatric lesional epilepsy surgery.
|
J Korean Med Sci
|
2012
|
0.78
|
|
36
|
Delayed posterior circulation insufficiency in pediatric moyamoya disease.
|
J Neurol
|
2014
|
0.78
|
|
37
|
Short-term efficacy and tolerability of rufinamide adjunctive therapy in children with refractory generalised epilepsy.
|
Epileptic Disord
|
2013
|
0.77
|
|
38
|
Subclinical hypothyroidism during valproic acid therapy in children and adolescents with epilepsy.
|
Neuropediatrics
|
2012
|
0.76
|
|
39
|
Involuntary movement in pediatric moyamoya disease patients: consideration of pathogenetic mechanism using neuroimaging studies.
|
Childs Nerv Syst
|
2013
|
0.76
|
|
40
|
Ischemic stroke in a 7-month-old infant with antiphospholipid antibody and homozygous C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism.
|
J Child Neurol
|
2010
|
0.76
|
|
41
|
Long-term surgical outcomes of temporal lobe epilepsy associated with low-grade brain tumors.
|
Cancer
|
2009
|
0.76
|
|
42
|
Glutaric aciduria type 1 in Korea: report of two novel mutations.
|
J Korean Med Sci
|
2010
|
0.75
|
|
43
|
A case of Becker muscular dystrophy with early manifestation of cardiomyopathy.
|
Korean J Pediatr
|
2012
|
0.75
|
|
44
|
Low incidence of SCN1A genetic mutation in patients with hemiconvulsion-hemiplegia-epilepsy syndrome.
|
Epilepsy Res
|
2013
|
0.75
|
|
45
|
Secondary leukemia in a child conceived using in vitro fertilization.
|
Pediatr Int
|
2008
|
0.75
|
|
46
|
Effects of lamotrigine on cognition and behavior compared to carbamazepine as monotherapy for children with partial epilepsy.
|
Brain Dev
|
2012
|
0.75
|
|
47
|
Andersen cardiodysrhythmic periodic paralysis with KCNJ2 mutations: a novel mutation in the pore selectivity filter residue.
|
J Child Neurol
|
2010
|
0.75
|
|
48
|
Severe cutaneous hypersensitivity to icodextrin in a continuous ambulatory peritoneal dialysis patient.
|
J Nephrol
|
2006
|
0.75
|
|
49
|
Infantile Pompe disease: clinical and genetic characteristics with an experience of enzyme replacement therapy.
|
J Child Neurol
|
2011
|
0.75
|
|
50
|
Coexisting seizures in patients with infantile spasms confirmed by long-term video-electroencephalography monitoring.
|
Epilepsy Res
|
2012
|
0.75
|
|
51
|
A 13-year-old girl with proximal weakness and hypertrophic cardiomyopathy with Danon disease.
|
Muscle Nerve
|
2010
|
0.75
|
|
52
|
Clinical and imaging findings of systemic hyalinosis: two cases presenting with congenital arthrogryposis.
|
Skeletal Radiol
|
2010
|
0.75
|
|
53
|
Rare coincidence of familial central core disease and hemophagocytic lymphohistiocytosis.
|
Pediatr Int
|
2014
|
0.75
|
|
54
|
A unique phenotype of 2q24.3-2q32.1 duplication: early infantile epileptic encephalopathy without mesomelic dysplasia.
|
J Child Neurol
|
2013
|
0.75
|
|
55
|
A single large-scale deletion of mtDNA in a child with recurrent encephalopathy and tubulopathy.
|
J Neurol Sci
|
2010
|
0.75
|
|
56
|
Comparison of flunarizine and topiramate for the prophylaxis of pediatric migraines.
|
Eur J Paediatr Neurol
|
2012
|
0.75
|