Published in Neuroradiology on March 21, 2014
Respiratory syncytial virus-related encephalitis: magnetic resonance imaging findings with diffusion-weighted study. Neuroradiology (2013) 2.62
Direct detection of respiratory syncytial virus, parainfluenza virus, and adenovirus in clinical respiratory specimens by a multiplex reverse transcription-PCR assay. J Clin Microbiol (1998) 2.42
Antibodies to N-methyl-D-aspartate glutamate receptors in Creutzfeldt-Jakob disease patients. J Neuroimmunol (2012) 1.03
Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures. Brain (2003) 2.44
Long-term course of Dravet syndrome: a study from an epilepsy center in Japan. Epilepsia (2014) 1.99
A novel treatment-responsive encephalitis with frequent opsoclonus and teratoma. Ann Neurol (2013) 1.50
HLA-B locus in Japanese patients with anti-epileptics and allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis. Pharmacogenomics (2008) 1.49
Refractory epilepsy accompanying acute encephalitis with multifocal cortical lesions: possible autoimmune etiology. Brain Dev (2007) 1.44
A chronic progressive case of enteroviral limbic encephalitis associated with autoantibody to glutamate receptor epsilon2. Eur Neurol (2007) 1.39
Fifty microdeletions among 112 cases of Sotos syndrome: low copy repeats possibly mediate the common deletion. Hum Mutat (2003) 1.38
Acute limbic encephalitis: a new entity? Neurosci Lett (2005) 1.35
A patient with epilepsia partialis continua with anti-glutamate receptor epsilon 2 antibodies. Pediatr Neurol (2003) 1.28
De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathy. Am J Hum Genet (2013) 1.27
Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency. Genet Med (2005) 1.25
Voltage-gated potassium channel complex antibodies in Creutzfeldt-Jakob disease. J Neurol (2012) 1.17
HLA-B*1511 is a risk factor for carbamazepine-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients. Epilepsia (2010) 1.16
Genomic copy number variations at 17p13.3 and epileptogenesis. Epilepsy Res (2010) 1.09
A mild form of adult-onset opsoclonus-myoclonus syndrome associated with antiglutamate receptor antibodies. JAMA Neurol (2013) 1.07
"Burst and slow complexes" in nonconvulsive epileptic status. Epileptic Disord (2006) 1.05
Risk factors for hyperammonemia associated with valproic acid therapy in adult epilepsy patients. Epilepsy Res (2012) 1.03
Antibodies to N-methyl-D-aspartate glutamate receptors in Creutzfeldt-Jakob disease patients. J Neuroimmunol (2012) 1.03
Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome. Pediatr Nephrol (2008) 1.02
CDKL5 alterations lead to early epileptic encephalopathy in both genders. Epilepsia (2011) 0.96
HLA class I markers in Japanese patients with carbamazepine-induced cutaneous adverse reactions. Epilepsia (2009) 0.95
Hypomyelination with atrophy of the basal ganglia and cerebellum in an infant with Down syndrome. Clin Dysmorphol (2011) 0.92
Reflex seizures in patients with malformations of cortical development and refractory epilepsy. Epilepsia (2005) 0.92
Vitamin B6-responsive epilepsy due to inherited GPI deficiency. Neurology (2013) 0.91
Human leukocyte antigen genotypes in carbamazepine-induced severe cutaneous adverse drug response in Japanese patients. J Dermatol (2008) 0.91
Acute encephalitis with refractory, repetitive partial seizures: case reports of this unusual post-encephalitic epilepsy. Brain Dev (2006) 0.91
Risk factors for hyperammonemia in pediatric patients with epilepsy. Epilepsia (2013) 0.91
Ophthalmoplegia and flaccid paraplegia in a patient with anti-NMDA receptor encephalitis: a case report and literature review. Intern Med (2013) 0.90
An immunologic case study of acute encephalitis with refractory, repetitive partial seizures. Brain Dev (2012) 0.90
Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic form: clinical course and phenotypic variations in four patients. Am J Med Genet A (2003) 0.89
Mortality in Dravet syndrome: search for risk factors in Japanese patients. Epilepsia (2011) 0.88
Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese population. J Hum Genet (2005) 0.88
Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndrome. Am J Hum Genet (2003) 0.88
Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome. Epilepsia (2011) 0.87
Various types of LRP5 mutations in four patients with osteoporosis-pseudoglioma syndrome: identification of a 7.2-kb microdeletion using oligonucleotide tiling microarray. Am J Med Genet A (2010) 0.87
A case of acute encephalitis with refractory, repetitive partial seizures, presenting autoantibody to glutamate receptor Gluepsilon2. Brain Dev (2005) 0.86
Craniosynostosis with extra copy of MSX2 in a patient with partial 5q-trisomy. Am J Med Genet A (2004) 0.86
[A case of non-herpetic acute encephalitis with autoantibodies for ionotropic glutamate receptor delta2 and epsilon2]. Rinsho Shinkeigaku (2005) 0.85
Detection of autoantibody against extracellular epitopes of N-methyl-D-aspartate receptor by cell-based assay. Neurosci Res (2011) 0.85
A case of acute cerebellitis accompanied by autoantibodies against glutamate receptor delta2. Brain Dev (2006) 0.85
Multifocal encephalopathy and autoimmune-mediated limbic encephalitis following tocilizumab therapy. Intern Med (2014) 0.85
Acute cerebellar ataxia and consecutive cerebellitis produced by glutamate receptor delta2 autoantibody. Brain Dev (2006) 0.85
Anti-N-methyl D-aspartate-type glutamate receptor antibody-positive limbic encephalitis in a patient with multiple sclerosis. Clin Neurol Neurosurg (2011) 0.85
Influence of CYP2C19 polymorphism and concomitant antiepileptic drugs on serum clobazam and N-desmethyl clobazam concentrations in patients with epilepsy. Ther Drug Monit (2013) 0.84
Paraneoplastic limbic encephalitis caused by ovarian teratoma with autoantibodies to glutamate receptor. Intern Med (2007) 0.84
Lamotrigine is favourable for startle-induced seizures. Epileptic Disord (2011) 0.83
Steroid-responsive chronic cerebellitis with positive glutamate receptor delta 2 antibody. J Child Neurol (2008) 0.83
Cerebrospinal fluid levels of cytokines in non-herpetic acute limbic encephalitis: comparison with herpes simplex encephalitis. Cytokine (2008) 0.83
Anti-glutamate receptor δ2 antibody-positive migrating focal encephalitis. Clin Neurol Neurosurg (2012) 0.83
Effects of oral administration of Lactobacillus acidophilus L-92 on the symptoms and serum cytokines of atopic dermatitis in Japanese adults: a double-blind, randomized, clinical trial. Int Arch Allergy Immunol (2015) 0.83
Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases. Brain Dev (2010) 0.83
[A child with non-herpetic acute limbic encephalitis affecting the claustrum and hippocampus]. No To Hattatsu (2006) 0.83
Steroid-responsive focal epilepsy with focal dystonia accompanied by glutamate receptor delta2 antibody. J Neuroimmunol (2012) 0.83
[Non-herpetic acute limbic encephalitis-like manifestation in a case of Hashimoto's encephalopathy with positive autoantibodies against ionotropic glutamate receptor epsilon2]. Rinsho Shinkeigaku (2007) 0.82
Early infantile manifestations of incontinentia pigmenti mimicking acute encephalopathy. Brain Dev (2010) 0.82
Association of acute cerebellar ataxia and human papilloma virus vaccination: a case report. Neuropediatrics (2013) 0.82
Expression of various glutamate receptors including N-methyl-D-aspartate receptor (NMDAR) in an ovarian teratoma removed from a young woman with anti-NMDAR encephalitis. Intern Med (2010) 0.82
Acute encephalopathy with refractory status epilepticus: bilateral mesial temporal and claustral lesions, associated with a peripheral marker of oxidative DNA damage. J Neurol Sci (2006) 0.82
A Young Man with Anti-NMDAR Encephalitis following Guillain-Barré Syndrome. Case Rep Neurol (2011) 0.82
Evaluation of serum cytokine levels in toxic epidermal necrolysis and Stevens-Johnson syndrome compared with other delayed-type adverse drug reactions. J Dermatol (2011) 0.82
Autoantibodies to glutamate receptor GluRepsilon2 in a patient with limbic encephalitis associated with relapsing polychondritis. J Neurol Sci (2009) 0.82
Specific HLA types are associated with antiepileptic drug-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese subjects. Pharmacogenomics (2013) 0.82
Influence of concomitant antiepileptic drugs on plasma lamotrigine concentration in adult Japanese epilepsy patients. Biol Pharm Bull (2012) 0.82
[Autoimmune encephalitis with anti-glutamate receptor antibody presenting as epilepsia partialis continua and action myoclonus: a case report]. Rinsho Shinkeigaku (2007) 0.81
Nationwide survey (incidence, clinical course, prognosis) of Rasmussen's encephalitis. Brain Dev (2009) 0.81
Stiripentol open study in Japanese patients with Dravet syndrome. Epilepsia (2009) 0.81
Epitope of autoantibodies to N-methyl-D-aspartate receptor heteromers in paraneoplastic limbic encephalitis. Ann Neurol (2008) 0.80
Influence of uridine diphosphate glucuronosyltransferase 2B7 -161C>T polymorphism on the concentration of valproic acid in pediatric epilepsy patients. Ther Drug Monit (2014) 0.79
ADORA2A polymorphism predisposes children to encephalopathy with febrile status epilepticus. Neurology (2013) 0.79
Twenty-one-year course of adult-onset Rasmussen's encephalitis and bilateral uveitis: case report. J Neurol Sci (2010) 0.79
Toxic epidermal necrolysis in a 4-year-old boy successfully treated with plasma exchange in combination with methylprednisolone and i.v. immunoglobulin. J Dermatol (2012) 0.79
Efficacy of stiripentol in hyperthermia-induced seizures in a mouse model of Dravet syndrome. Epilepsia (2012) 0.79
[Encephalitis associated with positive anti-GluR antibodies showing abnormal appearance in basal ganglia, pulvinar and gray matter on MRI--case report]. Rinsho Shinkeigaku (2011) 0.79
[Successful use of methylprednisolone therapy in a case of non-herpetic acute encephalitis with antibodies against ionotropic glutamate receptor epsilon2 and delta2]. Brain Nerve (2007) 0.79
A patient with early onset Huntington disease and severe cerebellar atrophy. Am J Med Genet A (2009) 0.79
PCDH19-related female-limited epilepsy: further details regarding early clinical features and therapeutic efficacy. Epilepsy Res (2013) 0.79
[Case of Vogt-Koyanagi-Harada disease associated with non-herpetic acute limbic encephalitis with autoantibodies against glutamate receptor epsilon2 in the cerebrospinal fluid]. Rinsho Shinkeigaku (2009) 0.78
Correspondence: A further case of opsoclonus-myoclonus syndrome associated with Mycoplasma pneumoniae infection. Eur J Pediatr (2009) 0.78
Detection of DNA of six human herpesviruses in the cerebrospinal fluid of immunocompetent non-herpetic acute limbic encephalitis patients. Microbiol Immunol (2010) 0.78
Clinical and radiological features of Japanese patients with a severe phenotype due to CASK mutations. Am J Med Genet A (2012) 0.78
Detection of anti-glutamate receptor ε2 and anti-N-methyl-D: -aspartate receptor antibodies in a patient with sporadic Creutzfeldt-Jakob disease. J Neurol (2011) 0.78
[A case of non-herpetic acute limbic encephalitis in childhood--comparison with acute encephalitis with refractory repetitive partial seizures (AERRPS)]. No To Hattatsu (2007) 0.78
Atypical Miller Fisher syndrome associated with glutamate receptor antibodies. BMJ Case Rep (2011) 0.77
Abnormal glucose metabolism in aromatic L-amino acid decarboxylase deficiency. Brain Dev (2009) 0.77
Anti-glutamate receptor ɛ2 antibodies in psychiatric patients with anti-thyroid autoantibodies--a prevalence study in Japan. Neurosci Lett (2012) 0.77
Acute cerebellitis following hemolytic streptococcal infection. Pediatr Neurol (2013) 0.77
Interstitial duplication of 2q32.1-q33.3 in a patient with epilepsy, developmental delay, and autistic behavior. Am J Med Genet A (2013) 0.77
Individualized phenytoin therapy for Japanese pediatric patients with epilepsy based on CYP2C9 and CYP2C19 genotypes. Ther Drug Monit (2015) 0.77
Temporal changes in brain MRI findings in Rasmussen syndrome. Epileptic Disord (2011) 0.77
MR imaging and 1H-MR spectroscopy of a case of van der Knaap disease. Brain Dev (2006) 0.77
Serum matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 levels in non-herpetic acute limbic encephalitis. J Neurol (2009) 0.77
A sensitive and simplified method to analyze free fatty acids in children with mitochondrial beta oxidation disorders using gas chromatography/mass spectrometry and dried blood spots. Clin Chim Acta (2002) 0.77
Encephalitis With Antibodies to GluN2B During Administration of Clozapine. Clin Neuropharmacol (2016) 0.77
[A case of chronic cerebellitis with anti-glutamate receptor delta 2 antibody]. No To Hattatsu (2004) 0.76
A case of anti-GA1 antibody-positive Fisher syndrome with elevated tau protein in cerebrospinal fluid. Brain Dev (2011) 0.76
[A case of persistent cerebellar ataxia complicated by conversion disorder--confirmed by positive cerebrospinal fluid glutamate receptor delta2 and epsilon2 antibodies]. No To Hattatsu (2011) 0.76
SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome. J Hum Genet (2011) 0.76
Increased interleukin-17 in the cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease: a case-control study of rapidly progressive dementia. J Neuroinflammation (2013) 0.76
[Development of rapid genotyping methods for single nucleotide polymorphisms of cytochrome P450 2C9 (CYP2C9) and cytochrome P450 2C19 (CYP2C19) and their clinical application in pediatric patients with epilepsy]. Yakugaku Zasshi (2011) 0.76