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2. Brivaracetam add-on treatment in pediatric patients with severe drug-resistant epilepsy: Italian real-world evidence

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

9. Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients

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

12. Epilepsy Course and Developmental Trajectories in STXBP1-DEE

13. Phenotypic Description of A Patient with ODLURO Syndrome and Functional Characterization of the Pathogenetic Role of A Synonymous Variant c.186G>A in KMT2E Gene.

15. Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants

18. Long‐term effectiveness of add‐on perampanel in patients with Lennox–Gastaut syndrome: A multicenter retrospective study

19. Perampanel as precision therapy in rare genetic epilepsies

20. A registry for Dravet syndrome: The Italian experience

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

27. Clinical and Functional Study of a De Novo Variant in the PVP Motif of Kv1.1 Channel Associated with Epilepsy, Developmental Delay and Ataxia

29. Brivaracetam in treating epileptic encephalopathy and refractory focal epilepsies in patients under 14 years of age

32. Stage of Change and Motivation to a Healthier Lifestyle before and after an Intensive Lifestyle Intervention

40. Early vagus nerve stimulator implantation as a main predictor of positive outcome in pediatric patients with epileptic encephalopathy

41. Bilateral facial nerve palsy in a child: When the smile returns

42. Glucose transporter type 1 deficiency syndrome: Developmental delay and early-onset ataxia in a novel mutation of the SLC2A1 gene

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