469 results on '"Toldo, Irene"'
Search Results
2. PPP3CA gene-related developmental and epileptic encephalopathy: Expanding the electro-clinical phenotype
3. Cortical Gyrification Is Associated With the Clinical Phenotype in Tuberous Sclerosis Complex
4. Corrigendum: The new Italian registry of infantile thrombosis (RITI): a reflection on its journey, challenges and pitfalls
5. The maturation of aperiodic EEG activity across development reveals a progressive differentiation of wakefulness from sleep
6. The new Italian registry of infantile thrombosis (RITI): A reflection on its journey, challenges and pitfalls
7. A systematic review of surgical and interventional radiology procedures for pediatric idiopathic intracranial hypertension.
8. Sleep disorders and neuropsychiatric disorders in a pediatric sample of tuberous sclerosis complex: a questionnaire-based study
9. Cerebral venous thrombosis and deep medullary vein thrombosis: Padua experience over the last two decades
10. Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD
11. Primary Stabbing Headache in Children and Adolescents
12. Mycophenolate mofetil, azathioprine and methotrexate usage in paediatric anti-NMDAR encephalitis: A systematic literature review
13. Treatment of Frequent or Chronic Primary Headaches in Children and Adolescents: Focus on Acupuncture
14. Pediatric Central Nervous System Tumors as Phenotypic Manifestation of Cancer Predisposition Syndromes
15. Pediatric and Adolescent Headache and Obesity
16. Brain malformations associated to Aldh7a1 gene mutations: Report of a novel homozygous mutation and literature review
17. Electroclinical features in two novel STRADA patients and a functional yeast assay for the validation of missense STRADA mutations
18. Rhinencephalon changes in tuberous sclerosis complex
19. Neonatal mitochondrial leukoencephalopathy with brain and spinal involvement and high lactate: expanding the phenotype of ISCA2 gene mutations
20. Hemiplegic Migraine in Children and Adolescents
21. Cold-Stimulus Headache in Children and Adolescents
22. Plasma exchange in pediatric anti-NMDAR encephalitis: A systematic review
23. Neonatal Arterial Ischemic Stroke Secondary to Carotid Artery Dissection: A Case Report and Systematic Literature Review
24. Myoclonic super-refractory status epilepticus with favourable evolution in a teenager with FIRES: Is the association of vagus nerve stimulation and cannabidiol effective?
25. EXTENDED GLASGOW OUTCOME SCALE TO EVALUATE THE FUNCTIONAL IMPAIRMENT OF PATIENTS WITH SUBCORTICAL BAND HETEROTOPIA: A MULTICENTRIC CROSS-SECTIONAL STUDY
26. Pacemaker in complicated and refractory breath-holding spells: When to think about it?
27. Pyridoxine-dependent epilepsies: an observational study on clinical, diagnostic, therapeutic and prognostic features in a pediatric cohort
28. Salivary glands abnormalities in oculo-auriculo-vertebral spectrum
29. Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD
30. Emotional Experience and Regulation in Juvenile Primary Headaches: A Cross-Sectional Pilot Study
31. Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort
32. Obesity and Migraine in Childhood
33. Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD
34. Long-term outcome of epilepsy in patients with Prader–Willi syndrome
35. Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort
36. Autoimmune Encephalitis and Other Neurological Syndromes With Rare Neuronal Surface Antibodies in Children: A Systematic Literature Review
37. Clinical guidelines in pediatric headache: evaluation of quality using the AGREE II instrument
38. Epilepsy in NF1: Epidemiologic, Genetic, and Clinical Features. A Monocentric Retrospective Study in a Cohort of 784 Patients
39. Short lasting activity-related headaches with sudden onset in children: a case-based reasoning on classification and diagnosis
40. Forkhead Box G1 Gene Haploinsufficiency: An Emerging Cause of Dyskinetic Encephalopathy of Infancy
41. Secondary parenchymal and vascular changes after middle cerebral artery stroke in children
42. Eating-induced epileptic spasms in a boy with MECP2 duplication syndrome: insights into pathogenesis of genetic epilepsies
43. Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?
44. Alexithymia in juvenile primary headache sufferers: a pilot study
45. Comorbidity between headache and epilepsy in a pediatric headache center
46. Headache in Children With Chiari I Malformation
47. A novel deletion in the GJA12 gene causes Pelizaeus–Merzbacher-like disease
48. sj-pdf-1-cep-10.1177_0333102420965139 - Supplemental material for I stay at home with headache. A survey to investigate how the lockdown for COVID-19 impacted on headache in Italian children
49. Erratum to: Oculo-auriculo-vertebral spectrum: going beyond the first and second pharyngeal arch involvement
50. Spinal cord and cauda equina MRI findings in metachromatic leukodystrophy: case report
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