European Journal of Paediatric Neurology

Papers
(The TQCC of European Journal of Paediatric Neurology is 5. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-05-01 to 2024-05-01.)
ArticleCitations
E.U. paediatric MOG consortium consensus: Part 1 – Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders87
European ad-hoc consensus statement on gene replacement therapy for spinal muscular atrophy73
E.U. paediatric MOG consortium consensus: Part 5 – Treatment of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders54
Severe Neurological Impairment: A delphi consensus-based definition45
Mid- and long-term (at least 12 months) follow-up of patients with spinal muscular atrophy (SMA) treated with nusinersen, onasemnogene abeparvovec, risdiplam or combination therapies: A systematic rev33
Efficacy of nusinersen in type 1, 2 and 3 spinal muscular atrophy: Real world data from Hungarian patients33
E.U. paediatric MOG consortium consensus: Part 2 – Neuroimaging features of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders32
E.U. paediatric MOG consortium consensus: Part 4 – Outcome of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders29
Melatonin for neuroprotection in neonatal encephalopathy: A systematic review & meta-analysis of clinical trials28
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients27
Children and young adults with spinal muscular atrophy treated with nusinersen27
Acute encephalitis in pediatric multisystem inflammatory syndrome associated with COVID-1926
Lissencephaly in an epilepsy cohort: Molecular, radiological and clinical aspects25
Evidence-based interventions for children and adolescents with fetal alcohol spectrum disorders – A systematic review25
Ankle foot orthoses in cerebral palsy: Effects of ankle stiffness on trunk kinematics, gait stability and energy cost of walking24
E.U. paediatric MOG consortium consensus: Part 3 – Biomarkers of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders24
Social cognition and executive functions in children and adolescents with focal epilepsy24
Mild Encephalitis/Encephalopathy with reversible splenial lesion syndrome: An unusual presentation of anti-GFAP astrocytopathy21
High association of MOG-IgG antibodies in children with bilateral optic neuritis21
Genetic causes underlying grey matter heterotopia21
CDKL5 deficiency disorder in males: Five new variants and review of the literature21
A practical approach to prenatal diagnosis of malformations of cortical development19
Neurodevelopmental outcomes of very preterm and very-low-birthweight infants in a population-based clinical cohort with a definite perinatal treatment policy19
Extra-uterine growth restriction in preterm infants: Neurodevelopmental outcomes according to different definitions19
Phenotypic spectrum of short-chain enoyl-Coa hydratase-1 (ECHS1) deficiency19
Lissencephaly: Update on diagnostics and clinical management18
Revision of the diagnostic criteria of alternating hemiplegia of childhood17
Exome sequencing in 57 patients with self-limited focal epilepsies of childhood with typical or atypical presentations suggests novel candidate genes17
Clinical spectrum and treatment outcome of 95 children with continuous spikes and waves during sleep (CSWS)17
Seizures during treatment of childhood acute lymphoblastic leukemia: A population-based cohort study17
Amplitude and stride-to-stride variability of muscle activity during Lokomat guided walking and treadmill walking in children with cerebral palsy16
The efficacy of endoscopic third ventriculostomy in children 1 year of age or younger: A systematic review and meta-analysis16
GATOR1-related focal cortical dysplasia in epilepsy surgery patients and their families: A possible gradient in severity?16
Neurologic manifestations in children with COVID-19 from a tertiary center in Turkey and literature review16
Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients15
Are morphological and structural MRI characteristics related to specific cognitive impairments in neurofibromatosis type 1 (NF1) children?15
Minor neurological signs and behavioural function at age 2 years in neonatal hypoxic ischaemic encephalopathy (HIE)15
The bottom-up approach: Non-invasive peripheral neurostimulation methods to treat migraine: A scoping review from the child neurologist's perspective15
Cerliponase alfa changes the natural history of children with neuronal ceroid lipofuscinosis type 2: The first French cohort14
Clinical phenotypes of infantile onset CACNA1A-related disorder14
Neurological presentations and cognitive outcome in Sturge-Weber syndrome14
Continuing decline in the prevalence of cerebral palsy in Denmark for birth years 2008–201314
Epidemiology of traumatic brain injury in children 15 years and younger in South-Eastern Norway in 2015–16. Implications for prevention and follow-up needs14
The phenotypic variability and natural history of NARS2 associated disease13
Rett Syndrome as a movement and motor disorder – A narrative review13
A recent surge of fulminant and early onset subacute sclerosing panencephalitis (SSPE) in the United Kingdom: An emergence in a time of measles13
Clinical features of paediatric and adult autoimmune encephalitis: A multicenter sample13
Qualitative and quantitative muscle ultrasound in patients with Duchenne muscular dystrophy: Where do sonographic changes begin?13
Acute monophasic erythromelalgia pain in five children diagnosed as small-fiber neuropathy12
Nusinersen does not improve lung function in a cohort of children with spinal muscular atrophy – A single-center retrospective study12
Perinatal inflammation is associated with social and motor impairments in preterm children without severe neonatal brain injury12
A comparison of the early motor repertoire of very preterm infants and term infants12
Cost-effectiveness of whole-exome sequencing in progressive neurological disorders of children12
Cognitive and neurological outcome of patients in the Dutch pyridoxine-dependent epilepsy (PDE-ALDH7A1) cohort, a cross-sectional study12
Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features12
Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy11
Health-related quality of life in children and adolescents with tuberous sclerosis complex and their caregivers: A multicentre cohort study from Germany11
Data-driven historical characterization of epilepsy-associated genes11
Pediatric recurrent acute necrotizing encephalomyelitis, RANBP2 genotype and Sars-CoV-2 infection: Diagnosis, pathogenesis and targeted treatments from a case study11
The prevalence and clinical relevance of hyperhomocysteinemia suggesting vitamin B12 deficiency in presumed healthy infants11
Clinical outcomes of pediatric Anti-NMDA receptor encephalitis11
Long-term cardiovascular safety of fenfluramine in patients with Dravet syndrome treated for up to 3 years: Findings from serial echocardiographic assessments11
Severe motion sickness in infants and children10
Evaluating next-generation sequencing in neuromuscular diseases with neonatal respiratory distress10
Motor outcome after perinatal stroke and early prediction of unilateral spastic cerebral palsy10
Usability and inter-rater reliability of the NeuroMotion app: A tool in General Movements Assessments10
The current practice regarding neuro-prognostication for comatose children after cardiac arrest differs between and within European PICUs: A survey10
Uncovering sleep in young males with Duchenne muscular dystrophy10
Migraine in children under 6 years of age: A long-term follow-up study10
Gait phenotype in Batten disease: A marker of disease progression10
Early initiation of ambroxol treatment diminishes neurological manifestations of type 3 Gaucher disease: A long-term outcome of two siblings10
Manifestation of migraine in adolescents: Does it change in puberty?10
Functional neurological movements in children: Management with a psychological approach9
Validation of the focal cerebral arteriopathy severity score (FCASS) in a Swiss cohort: Correlation with infarct volume and outcome9
Magnetic resonance imaging volumetric analysis in patients with Alternating hemiplegia of childhood: A pilot study9
Exploring sleep problems in young children with cerebral palsy - A population-based study9
Neonatal hypoxic-ischaemic encephalopathy: Motor impairment beyond cerebral palsy9
A nationwide study on Sydenham's chorea: Clinical features, treatment and prognostic factors9
Ocrelizumab in pediatric multiple sclerosis9
Hemimegalencephaly and tuberous sclerosis complex: A rare yet challenging association9
Is there a relationship between socioeconomic factors and prevalence, adherence and outcome in childhood epilepsy? A systematic scoping review9
Change in cross-sectional area of the median nerve with age in neonates, infants and children analyzed by high-resolution ultrasound imaging9
Deep brain stimulation in the management of paediatric neuropsychiatric conditions: Current evidence and future directions9
Developmental neurobiology of cerebellar and Basal Ganglia connections9
Acute-onset paralytic strabismus in toddlers is important to consider as a potential early sign of late-infantile Metachromatic Leukodystrophy8
Preoperative clinical symptomatology and stroke burden in pediatric moyamoya angiopathy: Defining associated risk variables8
Cognitive functioning and pain interference mediate pain predictive effects on health-related quality of life in pediatric patients with Neurofibromatosis Type 18
Functional outcomes of children with dyskinetic cerebral palsy depend on etiology and gestational age8
Quality of life and neurological disability in children and young people with ataxia telangiectasia8
Dystonia assessment in children with cerebral palsy and periventricular leukomalacia8
The myth of vaccination and autism spectrum8
Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes – A recognizable clinical phenotype8
Self-limited focal epilepsy and childhood apraxia of speech with WAC pathogenic variants8
Findings in susceptibility weighted imaging in pediatric patients with migraine with aura8
Motor learning in unilateral cerebral palsy and the influence of corticospinal tract reorganization8
Relationship between resting-state fMRI functional connectivity with motor and language outcome after perinatal brain injury – A systematic review8
Instrumented classification of patients with early onset ataxia or developmental coordination disorder and healthy control children combining information from three upper limb SARA tests8
Safety and recommendations for vaccinations of children with inborn errors of metabolism8
Language functions deserve more attention in follow-up of children born very preterm8
Adaptive skills and mental health in children and adolescents with neuromuscular diseases8
Solving the hypomyelination conundrum - Imaging perspectives7
CASK related disorder: Epilepsy and developmental outcome7
Implementation of Motor Function Measure score percentile curves - Predicting motor function loss in Duchenne muscular dystrophy7
Neonatal neurological examination in a resource-limited setting: What defines normal?7
Neurofilament light chain: A novel blood biomarker in patients with ataxia telangiectasia7
Prevalence and genetic subtypes of congenital myasthenic syndromes in the pediatric population of Slovenia7
MECP2-related conditions in males: A systematic literature review and 8 additional cases7
Posterior Reversible Encephalopathy Syndrome in infants and young children7
Rituximab in juvenile myasthenia gravis-an international cohort study and literature review7
Phenylalanine and tyrosine metabolism in DNAJC12 deficiency: A comparison between inherited hyperphenylalaninemias and healthy subjects7
Effect of age, cerebral infarcts, vasculopathy and haemoglobin on cognitive function, in Tanzanian children with sickle cell anaemia7
Diagnosis of pediatric anti-NMDAR encephalitis at the onset: A clinical challenge7
Migraine and epilepsy: Social cognition skills in pediatric population6
Melatonin usage in children and young adults, a registry-based cohort study6
MRI in CLN2 disease patients: Subtle features that support an early diagnosis6
The impact of instrumented gait analysis on decision-making in the interprofessional management of cerebral palsy: A scoping review6
Fenfluramine responder analyses and numbers needed to treat: Translating epilepsy trial data into clinical practice6
Tremor-like subcortical myoclonus in STXBP1 encephalopathy6
Natural history of TRPV4-Related disorders: From skeletal dysplasia to neuromuscular phenotype6
Neurocognitive profile of a cohort of SMA type 1 pediatric patients and emotional aspects, resilience and coping strategies of their caregivers6
Characterization of sedation and anesthesia complications in patients with alternating hemiplegia of childhood6
Effects of antiseizure monotherapy on visuospatial memory in pediatric age6
Neurological disorders encountered in a pediatric emergency department6
The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literature6
Updated clinical recommendations for the management of tuberous sclerosis complex associated epilepsy6
Development of muscle tone impairments in high-risk infants: Associations with cerebral palsy and cystic periventricular leukomalacia6
Endocrine and metabolic aspects of narcolepsy type 1 in children6
3T MRI signal intensity profiles and thicknesses of transient zones in human fetal brain at mid-gestation6
The impact of cerebral anomalies on cognitive outcome in patients with spina bifida: A systematic review6
Pediatric SMA patients with complex spinal anatomy: Implementation and evaluation of a decision-tree algorithm for administration of nusinersen6
CNTNAP1-encephalopathy: Six novel patients surviving the neonatal period5
Dystonia and choreoathetosis presence and severity in relation to powered wheelchair mobility performance in children and youth with dyskinetic cerebral palsy5
Long term perceptions of illness and self after Deep Brain Stimulation in pediatric dystonia: A narrative research5
Copy number variation in genetic epilepsy with febrile seizures plus5
Clinical features and blood iron metabolism markers in children with beta-propeller protein associated neurodegeneration5
Duplication/triplication mosaicism of EBF3 and expansion of the EBF3 neurodevelopmental disorder phenotype5
Ictal pouting (‘Chapeau de gendarme’) in three pediatric cases with cortical dysplasia5
Cognitive, academic, executive and psychological functioning in children with spastic motor type cerebral palsy: Influence of extent, location, and laterality of brain lesions5
Clinical characteristics of paediatric Hashimoto's encephalopathy5
Standardized motor assessments before the age of five predicting school-aged motor outcome including DCD: A systematic review5
Genetic testing in children enrolled in epilepsy surgery program. A real-life study5
Intranasal dexmedetomidine vs oral triclofos sodium for sedation of children with autism undergoing electroencephalograms5
Exome sequencing and electro-clinical features in pediatric patients with very early-onset retinal dystrophies: A cohort study5
Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center study5
Management of PHACES syndrome: Risk of stroke and its prevention from a neurosurgical perspective5
A Decision for Life – Treatment decisions in newly diagnosed families with spinal muscular atrophy (SMA)5
Management and results of epilepsy surgery associated with acyclovir prophylaxis in four pediatric patients with drug-resistant epilepsy due to herpetic encephalitis and review of the literature5
A vitamin a day keeps the doctor away: The need for high quality pyridoxal-5′-phosphate5
Brain morphological abnormalities in children with cyclin-dependent kinase-like 5 deficiency disorder5
Crisis of confidence in vaccination and the role of social media5
Prognostic value of brain abnormalities for cognitive functioning in cerebral palsy: A prospective cohort study5
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients5
Migraine in childhood: Gender differences5
The use of intrathecal baclofen for management of spasticity in hereditary spastic paraparesis: A case series5
Clinical features and outcomes of opsoclonus myoclonus ataxia syndrome5
Endovascular and thrombolytic treatment eligibility in childhood arterial ischemic stroke5
Abnormal heart rate variability at school age in survivors of neonatal hypoxic-ischemic encephalopathy managed with therapeutic hypothermia5
Surgical complications of intrathecal baclofen in children: A single centre, 20-year retrospective cohort study5
Prevalence of mental disorders in children and adolescents with cerebral palsy: Danish nationwide follow-up study5
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