870 results on '"Striano, Salvatore"'
Search Results
2. Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations
3. Reflex Seizures and Reflex Epilepsies
4. Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene
5. Epilepsy, cerebral calcifications, and gluten-related disorders: Are anti-transglutaminase 6 antibodies the missing link?
6. Familial adult myoclonic epilepsy: A new expansion repeats disorder
7. Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing
8. Provocative Factors
9. The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations
10. Does screening for adverse effects improve health outcomes in epilepsy?: A randomized trial
11. The challenges of treating epilepsy with 25 antiepileptic drugs
12. Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy
13. Genetics of reflex seizures and epilepsies in humans and animals
14. Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
15. Autosomal dominant lateral temporal epilepsy (ADLTE): Novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras
16. Seizures and EEG pattern in the 22q13.3 deletion syndrome: Clinical report of six Italian cases
17. Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?
18. Safety of Overnight Switch from Brand-Name to Generic Levetiracetam
19. Reflex myoclonic epilepsy in infancy: A multicenter clinical study
20. Alterations in the α2δ ligand, thrombospondin‐1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies
21. Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbidities.
22. Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series
23. Reflex seizures and reflex epilepsies: Old models for understanding mechanisms of epileptogenesis
24. The gelastic seizures-hypothalamic hamartoma syndrome: Facts, hypotheses, and perspectives
25. DRUG POINT: Chitosan may decrease serum valproate and increase the risk of seizure reappearance
26. A clinical and genetic study of 33 new cases with early-onset absence epilepsy
27. Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy
28. DRUG POINTS: Epileptic seizures can follow high doses of oral vardenafil
29. Off-Label Prescribing of Antiepileptic Drugs in Pharmacoresistant Epilepsy: A Cross-Sectional Drug Utilization Study of Tertiary Care Centers in Italy
30. In response: DEPDC5 mutations in epilepsy with auditory features
31. Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up
32. Efficacy of levetiracetam in the treatment of drug-resistant Rett syndrome
33. DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy
34. A prospective study of direct medical costs in a large cohort of consecutively enrolled patients with refractory epilepsy in Italy*
35. CHD2 variants are a risk factor for photosensitivity in epilepsy
36. Psychiatric features in gelastic epilepsy and hypothalamic hamartoma: long-term psychodiagnostic observations
37. Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome
38. Temporal lobe epilepsy and anti glutamic acid decarboxylase autoimmunity
39. Refractory, life-threatening status epilepticus in a 3-year-old girl
40. Autosomal dominant lateral temporal epilepsy: Absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins
41. Severe Epilepsy in An Adult with Partial Trisomy 18q
42. Copy number variations and susceptibility to lateral temporal epilepsy: A study of 21 pedigrees
43. Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study
44. Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy
45. Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families
46. Temporal‐parietal‐occipital epilepsy in GEFS+ associated with SCN1A mutation
47. Posterior reversible encephalopathy syndrome in intensive care medicine
48. Diagnosis and management of type 1 sialidosis: clinical insights from long-term care of four unrelated patients
49. Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation
50. Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy study
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