| Nome |
# |
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Neonatal developmental and epileptic encephalopathy due to autosomal recessive variants in SLC13A5 gene, file 91e78fff-94f7-4420-949f-96d2651e88bd
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41
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Long-term effectiveness of add-on perampanel in patients with Lennox-Gastaut syndrome: A multicenter retrospective study, file 245f7cf6-d31e-4402-8cce-224f3bfb1860
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21
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The Pharmacoresistant Epilepsy: An Overview on Existant and New Emerging Therapies, file 6f28a14c-02c4-40bf-ad91-9a9f63774388
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18
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Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD, file b3cffbfe-1a43-41eb-b5e3-33dd618cc4c2
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14
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A registry for Dravet syndrome: The Italian experience, file 4527f105-44e9-4aca-8ef0-88e7cbdf625a
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12
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The Ketogenic Diet for the Treatment of Mood Disorders in Comorbidity With Epilepsy in Children and Adolescents, file a3ad309f-299a-47b9-be4e-0de9565b33fe
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12
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Transition into adulthood: tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis, file ad1868e0-2779-4dfc-b59e-6cb70e5b4593
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11
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Monitoring And Managing Depression In Adolescents With Epilepsy: Current Perspectives, file 0a9055de-9abb-44bd-8f04-c5650be039de
|
9
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An unusual behavioural and motor paroxysmal disorder caused by insulinoma-related hypoglycemia: a possible cause of epilepsy misdiagnosis, file 9f5fe980-f4f5-400d-bb8c-bf95d6808705
|
9
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Understanding Childhood Neuroimmune Diseases of the Central Nervous System, file 4c838447-2a45-4cec-8327-b7522f5bb52d
|
8
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Neuroendocrine Effects on the Risk of Metabolic Syndrome in Children, file 3ac89272-5d9f-4159-8fe1-ef0b89f70542
|
7
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Cannabidiol in Pharmacoresistant Epilepsy: Clinical Pharmacokinetic Data From an Expanded Access Program, file 843ad23d-eb81-4a69-8a91-f151f7f8ced6
|
7
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Discovering a familial Xp11.4 microduplication: Does the mother matter?, file e4233f16-b92f-2860-e053-6605fe0a460a
|
7
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Effectiveness of Perampanel as the Only Add-on: Retrospective, Multicenter, Observational Real Life Study on epilepsy patients, file 1101087a-01bf-4a62-b561-fb1b82cbbfd6
|
6
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Polysomnographic Findings in Fragile X Syndrome Children with EEG Abnormalities, file 43b753a4-3cf2-4a0c-8487-5f7617389189
|
6
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Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study, file 2ce9e156-4ce2-4a0a-bd0e-8c39175a0cf0
|
5
|
|
Ketogenic diet for super-refractory status epilepticus (SRSE) with NORSE and FIRES: Single tertiary center experience and literature data, file 8ee16469-b25f-4a73-a159-11f482a9bd4b
|
5
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A nationwide study on Sydenham's chorea: Clinical features, treatment and prognostic factors, file 18365c59-1f11-4145-b7ea-7473ad8e1a62
|
3
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Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder, file 5cb1558f-dad0-4eac-89fc-8ffebfa1709d
|
3
|
|
Epileptic phenotypes in autoimmune encephalitis: from acute symptomatic seizures to autoimmune-associated epilepsy, file 9f8c2d45-a46a-453f-b075-e611b8914842
|
3
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Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities, file c0c674da-1551-498c-a112-0f43c6ad52ba
|
3
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Electroclinical features of epilepsy monosomy 1p36 syndrome and their implications, file 934a53bc-9ad2-4a9d-b8c1-dca43daf0461
|
2
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Perampanel Monotherapy for Focal and Generalized Epilepsy in Clinical Practice, file 9b26a506-4950-4f11-9011-22d39789a4cb
|
2
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Relapse risk factors in anti-N-methyl-D-aspartate receptor encephalitis, file b630d8f5-87a3-414f-9f52-df7d62ef897f
|
2
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Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variation, file 0079c2cf-99c8-493f-853b-2605ed7872e3
|
1
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Perisylvian, including insular, childhood epilepsy: Presurgical workup and surgical outcome, file 0ac28677-f945-4b2f-a921-2f18430a5cfc
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1
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Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication, file 147f8a95-4c55-4829-a75a-ed06ff03a76c
|
1
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|
Sleep disorders and neuropsychiatric disorders in a pediatric sample of tuberous sclerosis complex: a questionnaire-based study, file 1485657e-b345-442b-bf5b-e73c776a526c
|
1
|
|
Reflex myoclonic epilepsy in infancy: a critical review, file 1c83a531-5815-4b2a-9e21-b36ac4f6c19b
|
1
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|
Refractory absence seizures: An Italian multicenter retrospective study, file 3039f946-f839-43f9-ab9b-2b0610ddb403
|
1
|
|
Questionnaire-based assessment of sleep disorders in an adult population of Tuberous Sclerosis Complex, file 3eefdfca-e265-4c05-92f3-8a780669cb1e
|
1
|
|
Cognitive and neuropsychological evolution in children with anti-NMDAR encephalitis, file 424fc96b-05ac-46ec-b5ee-66e6fc6ddd68
|
1
|
|
Clinical and electroencephalographic features of epilepsy in patients with triple X syndrome: A case series, file 45b7c32c-27e7-4ca0-8785-b96ae7a781dd
|
1
|
|
Focal seizure, focal dyskinesia, or both? A complex motor phenomenon reveals anti-NMDAR encephalitis, file 493022e9-9d59-4d7a-b4a8-c9f5ce2b6bf8
|
1
|
|
Current advances in childhood absence epilepsy, file 52d975de-feae-46f6-81db-1f3e4d48f532
|
1
|
|
Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients, file 55884e77-9e7b-4893-9634-dd0a3d1ed206
|
1
|
|
Palliative non-resective surgery for drug-resistant epilepsy, file 5a293b3a-0f49-4a68-a9e1-6902983bdfad
|
1
|
|
Refractory absence epilepsy and glut1 deficiency syndrome: a new case report and literature review, file 5debd078-3866-48d7-913e-be1d68c52515
|
1
|
|
Efficacy and Safety of Fenfluramine in Epilepsy: A Systematic Review and Meta-analysis, file 60ea4d4b-7a8b-4789-b43b-96f446e5dd04
|
1
|
|
The dilemma of adult-onset Rasmussen encephalitis clinical assessment: Proposal for a new bedside tool to evaluate disease progression, file 62060fa4-1f03-45d0-84d8-c9ef1faec197
|
1
|
|
Epilepsy, electroclinical features, and long-term outcomes in Pitt-Hopkins syndrome due to pathogenic variants in the TCF4 gene, file 6474d081-164e-4910-a093-508b32e370be
|
1
|
|
Hemispherotomy in Rasmussen encephalitis: long-term outcome in an Italian series of 16 patients, file 70e567da-e72b-49a4-a158-dca9863eba92
|
1
|
|
The role of polytherapy in the management of epilepsy: suggestions for rational antiepileptic drug selection, file 77647fd8-5ce0-46e2-be7c-66baa7d7d0cc
|
1
|
|
Electroclinical features of epilepsy in patients with InvDup(15), file 7cbcf813-048f-4536-bc23-50bcf3d0bc13
|
1
|
|
Brivaracetam add-on treatment in pediatric patients with severe drug-resistant epilepsy: Italian real-world evidence, file 7f72c87c-4425-4b3a-9254-878d5b73fc0b
|
1
|
|
Social cognition and executive functions in children and adolescents with focal epilepsy, file 896b8b15-7734-461b-87db-fd38b1ab3eb2
|
1
|
|
Neuropsychological impairment in childhood absence epilepsy: Review of the literature, file 94e3aa63-fc62-4520-adf3-8ef712a0ed12
|
1
|
|
Memory impairment and Benign Epilepsy with centrotemporal spike (BECTS): a growing suspicion, file 95a0f792-1f17-453e-86ea-83843a8743af
|
1
|
|
Unraveling the enigma of new-onset refractory status epilepticus: a systematic review of aetiologies, file 966847ad-df07-4363-b984-0f3988111e43
|
1
|
|
Pharmacokinetic considerations for anti-epileptic drugs in children, file 9cd05a82-7241-4502-8cb0-c08d0cefac05
|
1
|
|
Epileptic phenotypes in children with early-onset mitochondrial diseases, file a237a296-0013-44a1-a587-0cef25023456
|
1
|
|
Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan-Herndon-Dudley Syndrome, file a2b2e12a-0994-4c28-a992-be0f6cff43ba
|
1
|
|
Efficacy and safety of vigabatrin in patients with tuberous sclerosis complex and infantile epileptic spasm syndrome: a systematic review, file a6b95385-9dfd-44b2-bf99-7f7ea9c02057
|
1
|
|
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study, file b17a00a2-5d83-4245-9ac1-339a3f309ba5
|
1
|
|
Clinical manifestations in children and adolescents with corpus callosum abnormalities, file bf189094-763d-4e44-b80d-238f4ed0284a
|
1
|
|
Perampanel tolerability in children and adolescents with focal epilepsy: Effects on behavior and executive functions, file c414c701-7126-4b1c-a05e-e5eb172a6d7f
|
1
|
|
First reported case of an inherited PACS2 pathogenic variant with variable expression, file c8cd633b-eb9b-437c-89fe-31344027ac0a
|
1
|
|
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15), file cabfb7a0-fbd8-4fca-b384-3d171235a299
|
1
|
|
Gain of function SCN1A disease-causing variants: Expanding the phenotypic spectrum and functional studies guiding the choice of effective antiseizure medication, file ccbd2f35-9622-474a-be9d-e7be6b5d38be
|
1
|
|
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications, file d4b1d6e4-06c5-47f1-8f7c-47c056511672
|
1
|
|
Potential role of brivaracetam in pediatric epilepsy, file d574074a-d393-4e12-af54-34067554dcd5
|
1
|
|
Pediatric NMDAR encephalitis: A single center observation study with a closer look at movement disorders, file d9735d4a-3dfc-487f-a398-603164e09489
|
1
|
|
Perampanel effectiveness and tolerability in patients with epilepsy at long-term follow-up, file d976e65d-4eb0-463a-8667-19bb832ccc48
|
1
|
|
Neuropsychological profiles and outcomes in children with new onset frontal lobe epilepsy, file e6875bcd-f0d9-49b2-8f96-630a87d1b3b4
|
1
|
|
Rufinamide for the treatment of refractory epilepsy secondary to neuronal migration disorders, file ea7a5854-c519-4c24-88e0-e3ffcce08e05
|
1
|
|
Anti-seizure medications for Lennox-Gastaut syndrome, file ed4d9cfe-5b30-41a2-b517-478a6d2eb138
|
1
|
|
Withdrawal seizures: possible risk factors, file efc6d5c1-c18a-4398-a62f-e24e14f4f546
|
1
|
|
Inflammation in pediatric epilepsies: Update on clinical features and treatment options, file fa1990c5-33f9-4540-b7d6-07531361da64
|
1
|
|
An Italian consensus on the management of Lennox-Gastaut syndrome, file ffaccb9f-a356-4fc7-8d00-9b6de53974d4
|
1
|
| Totale |
261 |