European Journal of Paediatric Neurology

Papers
(The H4-Index of European Journal of Paediatric Neurology is 19. 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 2020-11-01 to 2024-11-01.)
ArticleCitations
E.U. paediatric MOG consortium consensus: Part 1 – Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders97
E.U. paediatric MOG consortium consensus: Part 5 – Treatment of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders64
Severe Neurological Impairment: A delphi consensus-based definition57
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 rev52
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients37
E.U. paediatric MOG consortium consensus: Part 2 – Neuroimaging features of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders37
E.U. paediatric MOG consortium consensus: Part 4 – Outcome of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders34
Children and young adults with spinal muscular atrophy treated with nusinersen32
Acute encephalitis in pediatric multisystem inflammatory syndrome associated with COVID-1930
Lissencephaly in an epilepsy cohort: Molecular, radiological and clinical aspects30
Melatonin for neuroprotection in neonatal encephalopathy: A systematic review & meta-analysis of clinical trials29
Lissencephaly: Update on diagnostics and clinical management29
Evidence-based interventions for children and adolescents with fetal alcohol spectrum disorders – A systematic review26
Genetic causes underlying grey matter heterotopia26
CDKL5 deficiency disorder in males: Five new variants and review of the literature25
A practical approach to prenatal diagnosis of malformations of cortical development24
E.U. paediatric MOG consortium consensus: Part 3 – Biomarkers of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders24
Extra-uterine growth restriction in preterm infants: Neurodevelopmental outcomes according to different definitions22
GATOR1-related focal cortical dysplasia in epilepsy surgery patients and their families: A possible gradient in severity?20
Revision of the diagnostic criteria of alternating hemiplegia of childhood19
Neurologic manifestations in children with COVID-19 from a tertiary center in Turkey and literature review19
Amplitude and stride-to-stride variability of muscle activity during Lokomat guided walking and treadmill walking in children with cerebral palsy19
Neurological presentations and cognitive outcome in Sturge-Weber syndrome19
0.16362905502319