142 results on '"Gaggero R"'
Search Results
2. Mesial temporal sclerosis – a late complication in four allogeneic pediatric recipients with persistent seizures after an acute episode of cyclosporine-A neurotoxicity
3. Genetic Predisposition to Severe Myoclonic Epilepsy of Infancy (Dravet Syndrome): Analysis of Cases with and without SCNIA Mutations: 007
4. An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage disease
5. Distribution of epileptiform discharges during nREM sleep in the CSWSS syndrome: relationship with sigma and delta activities
6. Anti-NMDAR encephalitis misdiagnosed as Hashimoto's encephalopathy
7. Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy. Does 'SMEI plus' exist?
8. Inv dup (15): Clinical and electroencephalographic features in three cases
9. 6q terminal deletion: An emerging syndrome associated to a peculiar clinical and electroencephalographic picture
10. Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication
11. NOVEL MUTATIONS IN CDKL5 GENE, PREDICTED EFFECTS AND ASSOCIATED PHENOTYPES
12. USE OF LEVETIRACETAM FOR THE TREATMENT OF INFANTILE SPASMS
13. La genetica della sindrome di Dravet
14. Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families
15. Agenesia callosa, leucoipoplasia, ritardo mentale: una nuova sindrome
16. Malignant migrating partial seizures in infancy
17. Epilepsy associated with infantile hemiparesis: predictors of long term evolution
18. Felbamate in pediatric patients
19. Benzodiazepine (BDZ) treatment of benign childhood epilepsy with centrotemporal spikes (BECCT)
20. Early-onset progressive encephalopathy with migrant, continuous myoclonus
21. Felbamate in therapy-resistant epilepsy: An Italian experience
22. Farmaci anti-epilettici
23. The clinical use of dynamic EEG in childhood
24. An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy
25. Contributo della Computed EEG Topography (CET) allo studio delle epilessie infantili
26. la sindrome di ipernatremia neurogena nell'età evolutiva
27. Epilepsy with laughing seizures, hypothalamic hamartoma and precocious puberty. Contributions of MRI, computed EEG topography (CET) and ambulatory EEG (A-EEG)
28. Epilepsy and neuropsychological functions
29. Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy
30. Hashimoto's Encephalopathy with Selective Involvement of the Nucleus Accumbens: A Case Report
31. Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy
32. Severe neurologic complications after hematopoietic stem cell transplantation in children
33. 1. Severe neurological events (SNE) after bone marrow Transplantation (BMT) in children
34. 266 Epilepsy in children with mental retardation of undetermined origin
35. Discrepancies between ictal clinical and EEG features and MRI findings, in a case of drug-resistant partial epilepsy
36. Familial White Matter Hypoplasia, Agenesis of the Corpus Callosum, Mental Retardation and Growth Deficiency: A New Distinctive Syndrome
37. CSF Anomalies in Children Affected by Epilepsia Partialis Continua (EPC)
38. Cryptic chromosome deletions involving SCN1Ain severe myoclonic epilepsy of infancy
39. Malignant migrating partial seizures in infancy
40. A proposito delle classificazioni delle epilessie in età evolutiva: osservazioni e note (studio di 287 casi personali)
41. Secondary generalized epilepsy in childhood: EEG patterns and correlation with responsiveness to benzodiazepines or ACTH
42. 6q terminal deletion: An emerging syndrome associated to a peculiar clinical and electroencephalographic picture,La 6q terminal deletion realizza una sindrome elettroclinica e neuroradiologica peculiare
43. Epileptic discharges during sleep: A pathophysiological mechanism common to different clinical syndromes
44. Neurocutaneous melanosis and pharmacoresistant epilepsy: A difficult diagnosis,Melanosi neurocutanea ed epilessia farmacoresistente: Una diagnosi difficile
45. Epilepsy and anti-GAD in T1DM: Looking for a link,Epilessia e anti-GAD nei pazienti con DMT1: Esiste un link?
46. Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy. Does 'SMEI plus' exist?,Delezioni criptiche di 2q24.3-q31.1 coinvolgenti SCN1A in pazienti con epilessia mioclonica severa dell'infanzia. Esiste la 'SMEI plus'?
47. Intractable epilepsy secondary to cyclosporine toxicity in children undergoing allogeneic hematopoietic bone marrow transplantation
48. Clinical and electrophysiological features of Italian Neuronal Ceroid Lipofuscinosis patients with CLN8 mutations
49. Linkage analysis and disease models in benign familial infantile seizures (BFIS): A study of 16 families,Ereditarietà e fenotipo clinico in 16 famiglie con convulsioni infantili familiari benigne (BFIS)
50. Nearly continuous interictal epileptic discharges during sleep: A pathophysiological mechanism common to different clinical syndromes
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