79 results on '"Caraballo, Roberto"'
Search Results
2. Brivaracetam as add-on therapy in children with developmental epileptic encephalopathies: A study of 42 patients
3. Cannabidiol in children with treatment-resistant epilepsy with myoclonic-atonic seizures
4. Use of sulthiame as add-on therapy in children with non-self-limited focal epilepsies of childhood
5. Telemedicine for Individuals with epilepsy: Recommendations from the International League Against Epilepsy Telemedicine Task Force
6. CDKL5-associated developmental and epileptic encephalopathy: a long-term, longitudinal electroclinical study of 22 cases
7. Use of sulthiame as add-on therapy in children with myoclonic atonic epilepsy: A study of 35 patients
8. Vigabatrin-associated brain abnormalities on MRI and other neurological symptoms in patients with West syndrome
9. Panayiotopoulos syndrome: Unusual clinical manifestations
10. Long-term use of cannabidiol-enriched medical cannabis in a prospective cohort of children with drug-resistant developmental and epileptic encephalopathy
11. Status of epileptic spasms: A study of 21 children
12. Long-term effectiveness and adverse effects of ketogenic diet therapy in infants with drug-resistant epilepsy treated at a single center in Argentina
13. Cannabidiol-enriched medical cannabis as add-on therapy in children with treatment-resistant West syndrome: A study of eight patients
14. More than one self-limited epilepsy of childhood in the same patient: A multicenter study
15. Spontaneous remission of West syndrome associated with acute infection and fever in five patients
16. Clinical and molecular characterization of mitochondrial DNA disorders in a group of Argentinian pediatric patients
17. Self-limited epilepsy of childhood with affective seizures: A well-defined epileptic syndrome?
18. Self-limited epilepsy with centro-temporal spikes: A study of 46 patients with unusual clinical manifestations
19. West syndrome: A study of 26 patients receiving short-term therapy
20. Electroclinical pattern in the transition from West to Lennox-Gastaut syndrome
21. Telemedicine, drug-resistant epilepsy, and ketogenic dietary therapies: A patient survey of a pediatric remote-care program during the COVID-19 pandemic
22. Molecular diagnosis of epileptic encephalopathy of the first year of life applying a customized gene panel in a group of Argentinean patients
23. Telemedicine and epilepsy: A patient satisfaction survey of a pediatric remote care program
24. Effectiveness of cannabidiol in a prospective cohort of children with drug-resistant epileptic encephalopathy in Argentina
25. Corrigendum to “Effectiveness of cannabidiol in a prospective cohort of children with drug resistant epileptic encephalopathy in Argentina” [Seizure 80 (2020) 75–80]
26. The evolving indications of KD therapy
27. Rufinamide as add-on therapy in children with epileptic encephalopathies other than Lennox–Gastaut syndrome: A study of 34 patients
28. Childhood-only epilepsy with generalized tonic-clonic seizures: A well-defined epileptic syndrome
29. Strategy and Plan of Action for Epilepsy 2018
30. Sulthiame add-on therapy in children with Lennox-Gastaut syndrome: A study of 44 patients
31. Late-onset childhood neuronal ceroid lipofuscinosis: Early clinical and electroencephalographic markers
32. Ketogenic diet use in children with intractable epilepsy secondary to malformations of cortical development: A two- centre experience
33. Benign rolandic epilepsy and generalized paroxysms: A study of 13 patients
34. CLN2 disease (neuronal ceroid lipofuscinosis type 2): Experience in the real world with cerliponase alfa intracerebroventricular enzyme replacement therapy in a public hospital in Cordoba, Argentina
35. The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy
36. Epileptic spasms in clusters and associated syndromes other than West syndrome: A study of 48 patients
37. Epileptic spasms in clusters with focal EEG paroxysms: A study of 12 patients
38. Ketogenic diet in patients with epileptic encephalopathy with electrical status epilepticus during slow sleep
39. Encephalopathy with status epilepticus during sleep: Unusual EEG patterns
40. Ketogenic diet in pediatric patients with refractory focal status epilepticus
41. Epilepsy of infancy with migrating focal seizures: Six patients treated with bromide
42. Ketogenic diet in patients with Lennox–Gastaut syndrome
43. Landau–Kleffner syndrome: A study of 29 patients
44. Febrile infection-related epilepsy syndrome: A study of 12 patients
45. Encephalopathy with hemi-status epilepticus during sleep or hemi-continuous spikes and waves during slow sleep syndrome: A study of 21 patients
46. Encephalopathy with status epilepticus during sleep or continuous spikes and waves during slow sleep syndrome: A multicenter, long-term follow-up study of 117 patients
47. Rasmussen syndrome: An Argentinean experience in 32 patients
48. Epilepsy With Myoclonic Atonic Seizures: An Electroclinical Study of 69 Patients
49. Response
50. Electroclinical overlap of two types of epileptic encephalopathy occurring in the same children in a certain age period?
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