Published in Mult Scler on April 19, 2012
International Pediatric MS Study Group Clinical Trials Summit: meeting report. Neurology (2013) 0.89
Acute disseminated encephalomyelitis: current controversies in diagnosis and outcome. J Neurol (2015) 0.86
Myelin oligodendrocyte glycoprotein antibodies are associated with a non-MS course in children. Neurol Neuroimmunol Neuroinflamm (2015) 0.85
Multiple sclerosis in children: an update on clinical diagnosis, therapeutic strategies, and research. Lancet Neurol (2014) 0.85
Demyelinating and thrombotic diseases of the central nervous system: common pathogenic and triggering factors. Front Neurol (2015) 0.82
Therapeutic Approach to the Management of Pediatric Demyelinating Disease: Multiple Sclerosis and Acute Disseminated Encephalomyelitis. Neurotherapeutics (2016) 0.81
Epidemiology of multiple sclerosis in the pediatric population of Sardinia, Italy. Eur J Pediatr (2015) 0.78
Protocol for a multicentre randomiSed controlled TRial of IntraVEnous immunoglobulin versus standard therapy for the treatment of transverse myelitis in adults and children (STRIVE). BMJ Open (2015) 0.76
Acquired CNS Demyelinating Syndrome in Children Referred to ShirazPediatric Neurology Ward. Iran J Child Neurol (2014) 0.75
Paediatric Multiple Sclerosis: Update on Diagnostic Criteria, Imaging, Histopathology and Treatment Choices. Curr Neurol Neurosci Rep (2016) 0.75
A nationwide survey of pediatric acquired demyelinating syndromes in Japan. Neurology (2016) 0.75
Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria. Ann Neurol (2011) 25.66
Herpes simplex virus encephalitis in human UNC-93B deficiency. Science (2006) 4.26
Consensus definitions proposed for pediatric multiple sclerosis and related disorders. Neurology (2007) 4.23
Sex ratio of multiple sclerosis in Canada: a longitudinal study. Lancet Neurol (2006) 3.74
Differential diagnosis of suspected multiple sclerosis: a consensus approach. Mult Scler (2008) 3.28
Acute disseminated encephalomyelitis, multiphasic disseminated encephalomyelitis and multiple sclerosis in children. Brain (2000) 2.96
The changing demographic pattern of multiple sclerosis epidemiology. Lancet Neurol (2010) 2.81
Environmental factors and multiple sclerosis. Lancet Neurol (2008) 2.66
Using the two-source capture-recapture method to estimate the incidence of acute flaccid paralysis in Victoria, Australia. Bull World Health Organ (2002) 2.27
MRI parameters for prediction of multiple sclerosis diagnosis in children with acute CNS demyelination: a prospective national cohort study. Lancet Neurol (2011) 2.12
Incidence of acquired CNS demyelinating syndromes in a multiethnic cohort of children. Neurology (2011) 1.99
Role of MRI in the differentiation of ADEM from MS in children. Neurology (2008) 1.94
Clinical, environmental, and genetic determinants of multiple sclerosis in children with acute demyelination: a prospective national cohort study. Lancet Neurol (2011) 1.92
Natural history of multiple sclerosis with childhood onset. N Engl J Med (2007) 1.89
Multiple sclerosis in children: clinical diagnosis, therapeutic strategies, and future directions. Lancet Neurol (2007) 1.73
MRI in the diagnosis of pediatric multiple sclerosis. Neurology (2008) 1.73
Prognostic factors after a first attack of inflammatory CNS demyelination in children. Neurology (2008) 1.70
Multiple sclerosis in childhood: clinical features of 149 cases. Mult Scler (1997) 1.65
Incidence of acquired demyelination of the CNS in Canadian children. Neurology (2009) 1.63
Early relapse risk after a first CNS inflammatory demyelination episode: examining international consensus definitions. Dev Med Child Neurol (2007) 1.52
First episode of acute CNS inflammatory demyelination in childhood: prognostic factors for multiple sclerosis and disability. J Pediatr (2004) 1.48
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2. Am J Hum Genet (2009) 1.47
MRI prognostic factors for relapse after acute CNS inflammatory demyelination in childhood. Brain (2004) 1.31
Age at immigration to England of Asian and Caribbean immigrants and the risk of developing multiple sclerosis. J Neurol Neurosurg Psychiatry (1997) 1.16
Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan. Brain Dev (2009) 1.06
Paediatric multiple sclerosis and acute disseminated encephalomyelitis in Germany: results of a nationwide survey. Eur J Pediatr (2007) 1.04
Geography of hospital admissions for multiple sclerosis in England and comparison with the geography of hospital admissions for infectious mononucleosis: a descriptive study. J Neurol Neurosurg Psychiatry (2011) 0.93
Epidemiology of multiple sclerosis in Glasgow. Scott Med J (2004) 0.89
Childhood optic neuritis clinical features and outcome. Arch Dis Child (2010) 0.89
Severe acute disseminated encephalomyelitis: a paediatric intensive care population-based study. Mult Scler (2010) 0.87
The effect of gender in clinically isolated syndrome (CIS): a meta-analysis. Mult Scler (2011) 0.82
Revisions to the 2001 McDonald diagnostic criteria. Ann Neurol (2006) 0.82
Using multiple sources to improve and measure case ascertainment in surveillance studies: 20 years of the British Paediatric Surveillance Unit. J Public Health (Oxf) (2006) 0.82
Paediatric UK demyelinating disease longitudinal study (PUDDLS). BMC Pediatr (2011) 0.81
Paediatric multiple sclerosis: examining utility of the McDonald 2010 criteria. Mult Scler (2011) 0.77
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response. Nat Genet (2009) 5.84
British Infection Society guidelines for the diagnosis and treatment of tuberculosis of the central nervous system in adults and children. J Infect (2009) 3.92
Safety and efficacy of buccal midazolam versus rectal diazepam for emergency treatment of seizures in children: a randomised controlled trial. Lancet (2005) 3.84
Clinical and molecular phenotype of Aicardi-Goutieres syndrome. Am J Hum Genet (2007) 2.81
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature. Nat Genet (2012) 2.63
Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study. Lancet Neurol (2010) 2.60
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study. Lancet Neurol (2013) 2.36
Clinical diagnosis and assessment of severity of confirmed dengue infections in Vietnamese children: is the world health organization classification system helpful? Am J Trop Med Hyg (2004) 2.33
Incidence of Henoch-Schönlein purpura, Kawasaki disease, and rare vasculitides in children of different ethnic origins. Lancet (2002) 2.32
Management of suspected herpes simplex virus encephalitis in adults in a U.K. teaching hospital. Clin Med (2009) 2.29
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder. Brain (2010) 2.21
The effect of early human diet on caudate volumes and IQ. Pediatr Res (2008) 2.21
International Pediatric Multiple Sclerosis Study Group criteria for pediatric multiple sclerosis and immune-mediated central nervous system demyelinating disorders: revisions to the 2007 definitions. Mult Scler (2013) 2.20
Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigens. J Neurol Neurosurg Psychiatry (2012) 2.15
Acquired predisposition to mycobacterial disease due to autoantibodies to IFN-gamma. J Clin Invest (2005) 2.06
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2. Brain (2013) 1.93
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus. Nat Genet (2012) 1.82
Benign hereditary chorea related to NKX2.1: expansion of the genotypic and phenotypic spectrum. Dev Med Child Neurol (2013) 1.75
Impact of breast milk on intelligence quotient, brain size, and white matter development. Pediatr Res (2010) 1.71
Sonographic features of benign thyroid nodules: interobserver reliability and overlap with malignancy. J Ultrasound Med (2003) 1.70
The morphology and natural history of childhood cataracts. Surv Ophthalmol (2003) 1.68
Prophylactic antibiotics for the prevention of cellulitis (erysipelas) of the leg: results of the UK Dermatology Clinical Trials Network's PATCH II trial. Br J Dermatol (2011) 1.63
Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome. Dev Med Child Neurol (2013) 1.61
Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia. J Clin Invest (2009) 1.60
N-methyl-D-aspartate receptor antibodies in post-herpes simplex virus encephalitis neurological relapse. Mov Disord (2013) 1.55
A systematic review of the utility of electrodiagnostic testing in carpal tunnel syndrome. Br J Gen Pract (2002) 1.54
Evaluation of the World Health Organization standard tourniquet test and a modified tourniquet test in the diagnosis of dengue infection in Viet Nam. Trop Med Int Health (2002) 1.54
Encephalitis in children. Arch Dis Child (2011) 1.53
Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations. Dev Med Child Neurol (2013) 1.51
Indications and outcomes of deep anterior lamellar keratoplasty in children. Ophthalmology (2010) 1.51
Proinflammatory cytokines and chemokines in humans with Japanese encephalitis. J Infect Dis (2004) 1.48
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency). Brain (2010) 1.47
Amniotic membrane transplantation in children with symblepharon and massive pannus. Arch Ophthalmol (2006) 1.47
The prevalence of neurodevelopmental disorders in children prenatally exposed to antiepileptic drugs. J Neurol Neurosurg Psychiatry (2013) 1.45
Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35). Hum Mutat (2010) 1.44
Seizures and raised intracranial pressure in Vietnamese patients with Japanese encephalitis. Brain (2002) 1.44
Overlapping cortical malformations and mutations in TUBB2B and TUBA1A. Brain (2013) 1.40
Neonatal seizures: magnetic resonance imaging adds value in the diagnosis and prediction of neurodisability. Acta Paediatr (2014) 1.40
Are children with acute arterial ischaemic stroke eligible for hyperacute thrombolysis? A retrospective audit from a tertiary UK centre. Dev Med Child Neurol (2014) 1.39
Fifteen-minute consultation: The child with acute ataxia. Arch Dis Child Educ Pract Ed (2013) 1.39
A cohort study to assess the new WHO Japanese encephalitis surveillance standards. Bull World Health Organ (2008) 1.39
Congenital perisylvian dysfunction - is it a spectrum? Dev Med Child Neurol (2009) 1.38
Loss-of-function mutations in RAB18 cause Warburg micro syndrome. Am J Hum Genet (2011) 1.36
Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher disease. Brain (2005) 1.36
Late onset neurodegeneration in the Cln3-/- mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activation. Brain Res (2004) 1.32
Early onset seizures and Rett-like features associated with mutations in CDKL5. Eur J Hum Genet (2005) 1.32
Prevalence and predictors of vitamin D insufficiency in children: a Great Britain population based study. PLoS One (2011) 1.25
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations. Neuromuscul Disord (2010) 1.24
Health care professionals' views of paediatric outpatient non-attendance: implications for general practice. Fam Pract (2013) 1.22
Systematic review and meta-analysis of evidence for increasing numbers of drugs in antiretroviral combination therapy. BMJ (2002) 1.21
US of acute scrotal trauma: optimal technique, imaging findings, and management. Radiographics (2007) 1.19
Interferon alfa-2a in Japanese encephalitis: a randomised double-blind placebo-controlled trial. Lancet (2003) 1.19
Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum. Brain (2013) 1.19
Five-year experience of the 2-incision push-pull technique for anterior and posterior capsulorrhexis in pediatric cataract surgery. Ophthalmology (2006) 1.18
Phospholipase C beta 1 deficiency is associated with early-onset epileptic encephalopathy. Brain (2010) 1.18
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1. Am J Med Genet A (2015) 1.17
Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene. J Med Genet (2010) 1.16
Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13-14. Epilepsy Res (2002) 1.14
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis. Brain (2010) 1.13
Effect of delayed lumbar punctures on the diagnosis of acute bacterial meningitis in adults. Emerg Med J (2010) 1.12
Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome. J Physiol (2011) 1.12
Paediatric 'care closer to home': stake-holder views and barriers to implementation. Health Place (2012) 1.11
Immunosuppression alters disease severity in juvenile Batten disease mice. J Neuroimmunol (2011) 1.10
Mapping the brain in younger and older asymptomatic HIV-1 men: frontal volume changes in the absence of other cortical or diffusion tensor abnormalities. Cortex (2011) 1.09
Neurological manifestations of influenza infection in children and adults: results of a National British Surveillance Study. Clin Infect Dis (2013) 1.09
Cerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosis. Brain Res (2009) 1.08
Sheehan syndrome associated with raised intracranial pressure. J Neuroophthalmol (2013) 1.08
Digenic inheritance of mutations in FOXC1 and PITX2 : correlating transcription factor function and Axenfeld-Rieger disease severity. Hum Mutat (2011) 1.08
Childhood presentation of COL4A1 mutations. Dev Med Child Neurol (2012) 1.08
KCNJ10 mutations disrupt function in patients with EAST syndrome. Nephron Physiol (2011) 1.07
Autoantibody biomarkers in childhood-acquired demyelinating syndromes: results from a national surveillance cohort. J Neurol Neurosurg Psychiatry (2013) 1.07
Total brain white matter is a major determinant of IQ in adolescents born preterm. Ann Neurol (2011) 1.06
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses. Brain Pathol (2004) 1.04
Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency. J Med Genet (2012) 1.04
HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase. Orphanet J Rare Dis (2013) 1.03
Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination. Neurogenetics (2006) 1.02
Immune system irregularities in lysosomal storage disorders. Acta Neuropathol (2007) 1.02
Interhemispheric temporal lobe connectivity predicts language impairment in adolescents born preterm. Brain (2012) 1.01
T2 at MR imaging is an objective quantitative measure of cerebral white matter signal intensity abnormality in preterm infants at term-equivalent age. Radiology (2009) 1.01
Auditory interhemispheric transfer deficits, hearing difficulties, and brain magnetic resonance imaging abnormalities in children with congenital aniridia due to PAX6 mutations. Arch Pediatr Adolesc Med (2007) 1.01
Pilot survey of Hashimoto's encephalopathy in children. Dev Med Child Neurol (2005) 0.99
Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters. Am J Med Genet A (2011) 0.99
Incidence of cavernoma development in children after radiotherapy for brain tumors. J Neurosurg (2007) 0.98