19 results on '"Cesaroni, Carlo Alberto"'
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2. Early-onset dysphagia and severe neurodevelopmental disorder as early signs in a patient with two novel variants in NARS1: a case report and brief review of the literature
3. Tolosa-Hunt syndrome and recurrent painful ophthalmoplegic neuropathy, case reports: what to do and when?
4. Brivaracetam add-on treatment in pediatric patients with severe drug-resistant epilepsy: Italian real-world evidence
5. Guillain-Barrè Syndrome—Retrospective Analysis of Data from a Cohort of Patients Referred to a Tertiary Care Pediatric Neuromuscular Center from 2000 to 2017: Electrophysiological Findings, Outcomes, and a Brief Literature Review.
6. Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study
7. Severe Neurodevelopmental Disorder in Autosomal Recessive Spinocerebellar Ataxia 13 (SCAR13) Caused by Two Novel Frameshift Variants in GRM1
8. Tick-Borne Encephalitis in a 6-Year-Old Patient: A Case Report
9. Aromatic L-Amino-Acid Decarboxylase Deficiency Screening by Analysis of 3-O-Methyldopa in Dried Blood Spots: Results of a Multicentric Study in Neurodevelopmental Disorders
10. Posterior Cranial Fossa Malformation and Vascular Dysplasia in GJB2 Gene Mutation
11. Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures
12. Novel Insights from Clinical Practice: Xia-Gibbs Syndrome with Pes Cavus, Conjunctival Melanosis, and Eye Asymmetry due to a de novo AHDC1 Gene Variant – A Case Report and a Brief Review of the Literature.
13. Expanding Phenotype of SYT1-Related Neurodevelopmental Disorder: Case Report and Literature Review
14. Cannabidiol in the acute phase of Febrile Infection‐Related Epilepsy Syndrome ( FIRES )
15. Tick-Borne Encephalitis in a 6-Year-Old Patient: A Case Report
16. SUNCT/SUNA in Pediatric Age: A Review of Pathophysiology and Therapeutic Options
17. Association among Autistic Traits, Treatment Intensity and Outcomes in Adolescents with Anorexia Nervosa: Preliminary Results
18. Novel Insights from Clinical Practice: Xia-Gibbs Syndrome with Pes Cavus, Conjunctival Melanosis, and Eye Asymmetry due to a de novo AHDC1 Gene Variant – A Case Report and a Brief Review of the Literature
19. Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literature.
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