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 2021-06-01 to 2025-06-01.)
ArticleCitations
Analysis of the relation between cerebrospinal fluid antibody titers and clinical characteristics in pediatric patients with anti-N-methyl-D-aspartate receptor encephalitis74
‘Focal Seizures in Dystonic Cerebral Palsy (DCP): Rare or common or both?45
Urgent unmet need for pharmaceutical grade vitamin therapy in pyridoxine dependent epilepsies37
A life course perspective on mental disorders and psychopharmacologic drug use among persons living with cerebral palsy35
Spinal cord stimulation (SCS) induced favorable neuromodulative outcome in the treatment of chronic neuropathic pain syndrome in children32
Mental health and behaviour in children with dystonia: Anxiety, challenging behaviour and the relationship to pain and self-esteem32
Autoimmune encephalitis in Israeli children – A retrospective nationwide study31
Motor imagery ability of children with duchenne muscular dystrophy: Reliability and validity of kinesthetic and Visual Imagery Questionnaire-10, and its association with cognitive status29
Neurologic manifestations in children with COVID-19 from a tertiary center in Turkey and literature review28
Associations between muscle morphology and spasticity in children with spastic cerebral palsy27
The Utility of Creatine Kinase in Status Dystonicus and Pre-status dystonicus24
Endovascular and thrombolytic treatment eligibility in childhood arterial ischemic stroke24
The added value of multimodal neurophysiological tools in the prognostic assessment of perinatal hypoxic-ischemic encephalopathy23
Unmet health care needs over the first 2 years after pediatric traumatic brain injury22
Comparison of clinical characteristics between cluster and isolated seizures associated with benign convulsions with mild gastroenteritis22
Dysmature patterns of newborn EEG recordings: Biological markers of transitory brain dysfunction or brain injury22
Disruptive lesions can cause developmental anomalies in the fetal brain: Mini-review18
“Fidgety-like movements” in extremely preterm infants - A new entity of spontaneous movements18
Quality of life in young adolescents with epilepsy: A case control study18
Identification of novel pathogenic variants in the GCDH gene and assessment of neurodevelopmental outcomes in 24 children with glutaric aciduria type 118
Safety and recommendations for vaccinations of children with inborn errors of metabolism17
Efficacy and tolerability of Melatonin vs Triclofos to achieve sleep for pediatric electroencephalography: A single blinded randomized controlled trial15
Migraine and epilepsy: Social cognition skills in pediatric population15
The prevalence and clinical relevance of hyperhomocysteinemia suggesting vitamin B12 deficiency in presumed healthy infants15
Genetic causes of infection induced encephalitis14
Outcome measurement instruments in Rett syndrome: A systematic review14
Behavioral problems in infants and young children with spinal muscular atrophy and their siblings: A cross-sectional study14
The development of checklists and reference charts for activities of daily living of normal developing children14
Basal ganglia calcifications—etiological relationship to strokes from mild head trauma?13
Assessing communication, beyond just words13
Prevention of infantile spasms in tuberous sclerosis complex13
Opioid analgesia and temperature regulation are associated with EEG background activity and MRI outcomes in neonates with mild-to-moderate hypoxic-ischemic encephalopathy undergoing therapeutic hypoth13
GLUT1DS focus on dysarthria12
Developmental neurobiology of cerebellar and Basal Ganglia connections12
From childhood to adulthood: Long-term assessment of continuous intrathecal baclofen therapy in non-ambulant spastic cerebral palsy12
Respiratory function in LAMA2-related muscular dystrophy and SELENON-related congenital myopathy, a 1.5-year natural history study12
Cost-effectiveness of whole-exome sequencing in progressive neurological disorders of children12
Evidence-based interventions for children and adolescents with fetal alcohol spectrum disorders – A systematic review12
Exploring the connections between basal ganglia and cortex revealed by transcranial magnetic stimulation, evoked potential and deep brain stimulation in dystonia11
Gene therapy offers promise, but timing is crucial for SMA treatment11
Dystonia during hand activity in children with spastic unilateral cerebral palsy, an observational study11
Sphenoid dysplasia in patients with neurofibromatosis type 1: Clinical features and imaging findings including cerebrospinal fluid alterations11
Tumefactive demyelinating lesions: navigating the many faces of mimicry11
Plant-derived cannabinoids for treatment of spasticity in children and adolescents with severe cerebral palsy: Double-blind, placebo-controlled trial11
Letter to the Editor in response to Dr. Josef Finsterer et al. “Intense work-up is required for pediatric COVID-related acute necrotizing encephalopathy with RANBP2 variants”11
Experience of nusinersen treatment in advanced spinal muscular atrophy type 1: Characteristics of late responders with delayed treatment efficacy11
Piloting positive psychology resources for caregivers of a child with a genetic developmental and epileptic encephalopathy11
CSF-profile and hypocretin levels in children with narcolepsy type 1 and 210
Pediatric Neurotuberculosis: A cases series and review of the literature10
The association of serum vitamin D concentrations in paediatric migraine10
Cost-effective diagnosis for children with developmental and epileptic encephalopathy phenotype10
Instrumented classification of patients with early onset ataxia or developmental coordination disorder and healthy control children combining information from three upper limb SARA tests9
Clinical correlation between disease progression and central vein sign in pediatric onset multiple sclerosis: A binational study9
Behavioral, neurodevelopmental profile, and epilepsy trajectory in two series of SLC6A1-NDD: A retrospective study with comprehensive assessment, and a participatory database study9
Frequency of an intrathecal IgM synthesis and MRZ reaction in children with MS9
Ultra-rare ultra-care: Assessing the impact of caring for children with ultra rare diseases9
Folker Hanefeld, 1937–20229
Health-related quality of life in 153 children with neuromuscular disorders in Latin America: is it age, functional dependence or diagnosis?9
Provoked seizures might lead to a significant diagnosis delay in CLN29
Tremor-like subcortical myoclonus in STXBP1 encephalopathy9
Temporal trends in intraventricular hemorrhage in preterm infants: A Brazilian multicenter cohort9
Insights from European Reference Network for rare neurological disorders study surveys on diagnosis, treatment, and management of NKX2-1-related disorders9
Vertigo, pediatric migraine, and best treatment9
The choroid plexus as a diagnostic tool in Sturge-Weber syndrome9
Prognostic significance of ACTN3 genotype in Duchenne muscular dystrophy: Findings from an Argentine patient cohort9
It's easier to relearn gross motor skills than learn them for the first time after injury: Empirical evidence informing the age at injury debate9
Newborn screening in metachromatic leukodystrophy – European consensus-based recommendations on clinical management9
Fat embolism syndrome in Duchenne muscular dystrophy: Report on a novel case and systematic literature review9
Long term outcome in non-multiple sclerosis paediatric acquired demyelinating syndromes9
Editorial Board9
The promise of personalized medicine in pediatric epilepsy – The time has come9
Intense work-up is required for pediatric COVID-related acute necrotizing encephalopathy with RANBP2 variants8
Similar disease progression in nonsense Duchenne muscular dystrophy boys as general natural history: Single Brazilian center 15 years registry view8
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 rev8
Movement disorders, cerebral palsy and vaccination8
ATP1A3-related disorders in the differential diagnosis of acute brainstem and cerebellar dysfunction8
Pathological gait in Rett syndrome: Quantitative evaluation using three-dimensional gait analysis8
Epidemiology of paediatric moderate and severe traumatic brain injury in the Netherlands8
Comprehensive neurological evaluation of a cohort of patients with neurofibromatosis type 1 from a single institution8
Reliability and validity of a newly developed PANDAS/PANS questionnaire8
A practical approach to prenatal diagnosis of malformations of cortical development8
A novel family illustrating the mild phenotypic spectrum of TUBB2B variants8
Ocrelizumab in pediatric patients with MS: Efficacy, tolerability, and safety7
Are atypical knee jerk responses prognostic for cerebral palsy in high-risk infants and children?7
Neurophysiological recordings improve the accuracy of the evaluation of the outcome in perinatal hypoxic ischemic encephalopathy7
Is ketogenic diet a ‘precision medicine’? Recent developments and future challenges7
Neurologic manifestations in children with COVID-197
Facilitation of drug-resistant epilepsy and catastrophic status epilepticus in children with combined pituitary hormone deficiency7
Vaccination and childhood epilepsies7
Visual outcome measures in pediatric myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD)7
Deep brain stimulation for phantom limb pain7
Autonomic risks in Alternating Hemiplegia of Childhood7
Endocrine and metabolic aspects of narcolepsy type 1 in children7
Predicting respiratory failure and outcome in pediatric Guillain-Barré syndrome7
Outcomes for patients in the RESTORE registry with spinal muscular atrophy and four or more SMN2 gene copies treated with onasemnogene abeparvovec7
Harmful metabolic acidosis in children treated by ketogenic diet during prolonged general anesthesia for epilepsy surgery: A single center experience6
Myotonic dystrophy type 1 (Steinert disease): 29 years of experience at a tertiary pediatric hospital6
“Deconstructing” upper limb function in dyskinetic cerebral palsy6
Reduced elbow muscle strength in children and adolescents with Charcot-Marie-Tooth disease: a case control study6
Identification of PMD subgroups using a myelination score for PMD6
Melatonin usage in children and young adults, a registry-based cohort study6
Neurological and psychiatric phenotype of a multicenter cohort of patients with SETD5-related neurodevelopmental disorder6
Clinical features and outcomes of opsoclonus myoclonus ataxia syndrome6
Advances in genetics: The start of a new stage for management of focal cortical malformations6
Room to improve: The diagnostic journey of Spinal Muscular Atrophy6
Bradykinesia assessment in children with cerebral palsy and periventricular leukomalacia6
Long-term monitoring of children with Pseudo Tumor Cerebri Syndrome by transbulbar sonography6
Starting a DBS service for children: It’s not the latitude but the attitude - Establishment of the paediatric DBS centre in Northern Finland6
Understanding North Star Ambulatory Assessment total scores and their implications for standards of care using observational data6
Frequency and clinical relevance of MOG-antibodies in CSF in pediatric patients with MOG antibody-associated diseases6
Clinical and radiological findings of posterior reversible encephalopathy syndrome in children: About 16 children hospitalized in the pediatric department of a Tunisian tertiary care hospital6
Neurological presentations and cognitive outcome in Sturge-Weber syndrome6
Serum Neurofilament light chain (NfL) levels in children with and without neurologic diseases5
Reassuring neuropsychological outcome data in myelin oligodendrocyte glycoprotein antibody-associated disease5
Unravelling key pathways in childhood ataxia to guide diagnosis and treatment5
Transcranial magnetic stimulation in children with fetal alcohol spectrum disorder: A randomised, crossover pilot-trial5
Developmental and epileptic encephalopathy 56 due to YWHAG variants: 12 new cases and review of the literature5
Editorial Board5
Monocentric retrospective clinical outcome in a group of 13 patients with opsoclonus myoclonus syndrome, proposal of diagnostic algorithm and review of the literature5
Approach to childhood tremors: Insights from a pediatric neurologist5
Editorial Board5
Corrigendum to “Pediatric SMA patients with complex spinal anatomy: Implementation and evaluation of a decision-tree algorithm for administration of nusinersen”[ Eur. J. Paediatr. Neurol. (2021) 92–105
Pediatric-onset multiple sclerosis in Greece: A single-center study of the risk factors and a review of the literature5
The long-term burden of congenital cytomegalovirus: Hospitalisation and mortality in a population-based matched cohort study5
Phenotypic expansion of EGP5-related Vici syndrome: 15 Dutch patients carrying a founder variant5
Dystonia following acquired brain injury (ABI) in childhood – Not as common as we might think?5
Speckled brain lesions in Incontinentia Pigmenti patients with acquired brain syndromes5
Lesion size and long-term cognitive outcome after pediatric stroke: A comparison between two techniques to assess lesion size5
Efficacy and safety of Nusinersen among children with spinal muscular atrophy from North India: A prospective cohort study (NICE-SMA study)5
Acute encephalitis in pediatric multisystem inflammatory syndrome associated with COVID-195
MECP2-related conditions in males: A systematic literature review and 8 additional cases5
Refining revascularization surgery indications for paediatric moyamoya angiopathy: Age also matters5
The use of intrathecal baclofen for management of spasticity in hereditary spastic paraparesis: A case series5
Cognitive development after perinatal unilateral infarctions: No evidence for preferential sparing of verbal functions5
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