34 results on '"Praticò, Andrea D"'
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2. Polymicrogyria, Cobblestone Malformations, and Tubulin Mutation (Overmigration beyond Pial Limiting Membrane): Diagnosis, Treatment, and Rehabilitation Approach
3. Periventricular Heterotopias: Neuroependymal Abnormalities
4. Microcephaly and Its Related Syndromes: Classification, Genetic, Clinical, and Rehabilitative Considerations
5. Introduction: A Practical Guide to Central Nervous System Malformations—From Genetics, to Diagnosis and Treatment
6. Anomalies of the Mesenchyme (Meninges and Skull)—Defects of Neural Tube Closure: Cephalocele and Other Calvarial and Skull Base Defects; Intracranial Lipomas; Arachnoid Cysts; Nonsyndromic and Syndromic Craniosynostoses
7. Holoprosencephaly: The Disease and Its Related Disabilities
8. Megalencephaly: Classification, Genetic Causes, and Related Syndromes
9. Congenital/Primitive Hydrocephalus: Classification, Clinical Aspects, and Rehabilitation Approach
10. Foreword: A Special Issue on Central Nervous System Malformations
11. The Atlas of Monogenic Epilepsies
12. DNM1 Gene and Its Related Epileptic Phenotypes
13. FOXG1 Gene and Its Related Phenotypes
14. KCNT1-Related Epilepsy: A Review
15. SYNGAP1 and Its Related Epileptic Syndromes
16. TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype
17. GRIN2A and GRIN2B and Their Related Phenotypes
18. PCDH19-Related Epilepsies
19. Erratum: SCN2A and Its Related Epileptic Phenotypes
20. Erratum: Monogenic Epilepsies: Channelopathies, Synaptopathies, mTorpathies, and Otheropathies
21. CDKL5 Gene: Beyond Rett Syndrome
22. Aristaless-Related Homeobox (ARX): Epilepsy Phenotypes beyond Lissencephaly and Brain Malformations
23. SCN1A and Its Related Epileptic Phenotypes
24. Syntaxin Binding Protein 1 Related Epilepsies
25. WDR45 Gene and Its Role in Pediatric Epilepsies
26. The Spectrum of KCNQ2- and KCNQ3-Related Epilepsy
27. SCN1B Gene: A Close Relative to SCN1A
28. Monogenic Epilepsies: Channelopathies, Synaptopathies, mTorpathies, and Otheropathies
29. Gamma-Aminobutyric Acid Type A Receptor Genes and Their Related Epilepsies
30. SCN2A and Its Related Epileptic Phenotypes
31. Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause–Effect Hypothesis
32. Reconstructive Surgery in Children with Down Syndrome: Bioethical Implications
33. Aicardi–Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations
34. Clinical Course of N-Methyl-D-Aspartate Receptor Encephalitis and the Effectiveness of Cyclophosphamide Treatment
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