28 results on '"Hollody, Katalin"'
Search Results
2. Has the Incidence of Febrile Convulsions in Childhood Changed During the SARS-CoV-2 Pandemic?
3. The training and organization of Paediatric Neurology in Europe: Special report of the European Paediatric Neurology Society & Committee of National Advisors
4. Classification of events contributing to postneonatal cerebral palsy: Development, reliability, and recommendations for use.
5. Epileptic seizure or not? Proportion of correct judgement based only on a video recording of a paroxysmal event
6. Increased resting-state EEG functional connectivity in benign childhood epilepsy with centro-temporal spikes
7. Trends in Prevalence and Characteristics of Post-Neonatal Cerebral Palsy Cases: A European Registry-Based Study
8. Trends in prevalence and characteristics of post-neonatal cerebral palsy cases: A European registry-based study
9. MRI classification system (MRICS) for children with cerebral palsy: development, reliability, and recommendations
10. Early-onset binocularity in preterm infants reveals experience-dependent visual development in humans
11. Does vigabatrin treatment for infantile spasms cause visual field defects? An international multicentre study
12. Imaging the cortical effect of lamotrigine in patients with idiopathic generalized epilepsy: A low-resolution electromagnetic tomography (LORETA) study
13. Quantitative EEG effects of carbamazepine, oxcarbazepine, valproate, lamotrigine, and possible clinical relevance of the findings
14. Paroxysmal non‐epileptic events in infancy: five cases with typical features
15. Children and adolescents with cerebral palsy have reliable knowledge about their own condition - Self- and parent reported quality of life
16. Staged Bilateral Stereotactic Pallidothalamotomy for Life-Threatening Dystonia in a Child With Hallervorden–Spatz Disease
17. Clinical features of cerebral palsy in children with symptomatic congenital cytomegalovirus infection
18. Does vigabatrin treatment for infantile spasms cause visual field defects? An international multicentre study
19. Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations
20. Mitochondrial dysfunction and organic aciduria in five patients carrying mutations in the Ras-MAPK pathway
21. Delayed speech development with facial asymmetry
22. Staged bilateral stereotactic pallidothalamotomy for life‐threatening dystonia in a child with Hallervorden–Spatz disease
23. Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
24. Mitochondrial dysfunction and organic aciduria in five patients carrying mutations in the Ras-MAPK pathway.
25. The training and organization of Paediatric Neurology in Europe: Special report of the European Paediatric Neurology Society & Committee of National Advisors
26. Multicenter retrospective study of patients with PCDH19-related epilepsy: The first Hungarian cohort.
27. Prevalence, Clinical Features, Neuroimaging, and Genetic Findings in Children With Ataxic Cerebral Palsy in Europe.
28. Anti-N-methyl-D-aspartate receptor encephalitis and drug abuse - the probable role of molecular mimicry or the overstimulation of CB receptors in a 17-year-old adolescent - case report.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.