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2. Drug resistant epilepsies: A multicentre case series of steroid therapy

5. An Italian consensus on the management of Lennox-Gastaut syndrome

9. Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations

10. Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European study

11. The management of epilepsy in clinical practice: Do the timing and severity of the disease influence the priorities of patients and the caring physicians? Data from the EPINEEDS study

15. Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations

19. Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform

25. Lacosamide in pediatric and adult patients: Comparison of efficacy and safety

27. Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy

32. Autosomal dominant lateral temporal epilepsy: Absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins

39. Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism

40. No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy

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