18 results on '"Gennaro, Elena"'
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2. Mild Lafora disease: Clinical, neurophysiologic, and genetic findings
3. Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance
4. Electroclinical presentation and genotype–phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations
5. SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis
6. Brain MRI Findings in Severe Myoclonic Epilepsy in Infancy and Genotype–Phenotype Correlations
7. Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations
8. Linkage Analysis and Disease Models in Benign Familial Infantile Seizures: A Study of 16 Families
9. Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease
10. Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation
11. Exploration of a Putative Susceptibility Locus for Idiopathic Generalized Epilepsy on Chromosome 8p12
12. Lack of SCN1A Mutations in Familial Febrile Seizures
13. No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12-q13.1
14. A novel c132-134del mutation in Unverricht-Lundborg disease and the review of literature of heterozygous compound patients
15. Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygousCSTBpoint and indel mutations
16. SCN1Aduplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis
17. Brain MRI Findings in Severe Myoclonic Epilepsy in Infancy and Genotype?Phenotype Correlations
18. Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations.
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