563 results on '"Striano, Salvatore"'
Search Results
2. Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene
3. Epilepsy, cerebral calcifications, and gluten-related disorders: Are anti-transglutaminase 6 antibodies the missing link?
4. Familial adult myoclonic epilepsy: A new expansion repeats disorder
5. The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations
6. Does screening for adverse effects improve health outcomes in epilepsy?: A randomized trial
7. The challenges of treating epilepsy with 25 antiepileptic drugs
8. Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy
9. Genetics of reflex seizures and epilepsies in humans and animals
10. Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
11. Autosomal dominant lateral temporal epilepsy (ADLTE): Novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras
12. Seizures and EEG pattern in the 22q13.3 deletion syndrome: Clinical report of six Italian cases
13. Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?
14. Safety of Overnight Switch from Brand-Name to Generic Levetiracetam
15. Reflex myoclonic epilepsy in infancy: A multicenter clinical study
16. Alterations in the α2δ ligand, thrombospondin‐1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies
17. Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbidities.
18. Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series
19. Reflex seizures and reflex epilepsies: Old models for understanding mechanisms of epileptogenesis
20. The gelastic seizures-hypothalamic hamartoma syndrome: Facts, hypotheses, and perspectives
21. DRUG POINT: Chitosan may decrease serum valproate and increase the risk of seizure reappearance
22. A clinical and genetic study of 33 new cases with early-onset absence epilepsy
23. Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy
24. DRUG POINTS: Epileptic seizures can follow high doses of oral vardenafil
25. Off-Label Prescribing of Antiepileptic Drugs in Pharmacoresistant Epilepsy: A Cross-Sectional Drug Utilization Study of Tertiary Care Centers in Italy
26. In response: DEPDC5 mutations in epilepsy with auditory features
27. Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up
28. Efficacy of levetiracetam in the treatment of drug-resistant Rett syndrome
29. DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy
30. A prospective study of direct medical costs in a large cohort of consecutively enrolled patients with refractory epilepsy in Italy*
31. CHD2 variants are a risk factor for photosensitivity in epilepsy
32. Psychiatric features in gelastic epilepsy and hypothalamic hamartoma: long-term psychodiagnostic observations
33. Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome
34. Temporal lobe epilepsy and anti glutamic acid decarboxylase autoimmunity
35. Refractory, life-threatening status epilepticus in a 3-year-old girl
36. Autosomal dominant lateral temporal epilepsy: Absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins
37. Severe Epilepsy in An Adult with Partial Trisomy 18q
38. Copy number variations and susceptibility to lateral temporal epilepsy: A study of 21 pedigrees
39. Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study
40. Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families
41. Posterior reversible encephalopathy syndrome in intensive care medicine
42. Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation
43. Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy study
44. Posterior reversible encephalopathy syndrome (PRES) in critically ill obstetric patients
45. Clinical dissection of early onset absence epilepsy in children and prognostic implications
46. Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy
47. Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death
48. Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations
49. Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion
50. Clinical Significance of Rare Copy Number Variations in Epilepsy: A Case-Control Survey Using Microarray-Based Comparative Genomic Hybridization
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