About: Federico Vigevano

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researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) 研究者 (ja) дослідник (uk) onderzoeker (nl)
rdfs:label	Federico Vigevano (en) Federico Vigevano (nl) Federico Vigevano (ast)
skos:prefLabel	Federico Vigevano (en) Federico Vigevano (nl) Federico Vigevano (ast)
name	Federico Vigevano (en) Federico Vigevano (nl) Federico Vigevano (ast)
Scopus author ID	wds:Q89961005-CE93FEC2-8E49-4451-9548-433BBC12FDC7
Scopus author ID	7005193957
given name	wds:Q89961005-C6DCD943-910A-4845-AE09-FEE7D9393C85
given name	Federico
instance of	wds:Q89961005-9267B07E-484E-4F96-9171-DB3B8D9A6C4D
instance of	Homo sapiens
occupation	wds:Q89961005-9A18327F-AF62-4DB5-B1E1-F3D80A2E53F4
employer	wds:Q89961005-214ED472-AFE6-40E3-85CB-FA66911F5094
sex or gender	wds:Q89961005-b4893d49-fc19-4495-b311-5ab2b691afda
VIAF ID	wds:Q89961005-8713351e-a5c7-4400-8ff7-75f4ac37f219
IdRef ID	wds:Q89961005-26B0DF4A-CB77-4A76-949C-74034D3222B9
SHARE Catalogue author ID	wds:Q89961005-D312CDF4-6CA8-463E-841A-2050D9D9F11A
family name	wds:Q89961005-CCC632CB-B372-401D-A7B2-CCEACA0B524F
National Library of Israel J9U ID	wds:Q89961005-FB2D2E98-2C8F-4C38-9ECB-3FF7EB3D96E7
VIAF ID	http://viaf.org/viaf/23682437
IdRef ID	http://www.idref.fr/201466066/id
occupation	researcher
employer	Bambino Gesù Hospital
sex or gender	male
VIAF ID	23682437
IdRef ID	201466066
SHARE Catalogue author ID	295949
family name	Vigevano
National Library of Israel J9U ID	987007316165805171
ORCID iD	wds:Q89961005-681597C4-93FA-426A-92F0-2C9659845A1B
ORCID iD	https://orcid.org/0000-0001-7513-0051
ORCID iD	0000-0001-7513-0051
ResearcherID	wds:Q89961005-0FF34301-21F6-4982-9E06-BC475142ADA1
ResearcherID	K-9466-2016
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q89961005
is author of	Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy Levetiracetam in juvenile myoclonic epilepsy: long-term efficacy in newly diagnosed adolescents. Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations. Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance. Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations. Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy Clinical features, anger management and anxiety: a possible correlation in migraine children Migraine equivalents and related symptoms, psychological profile and headache features: which relationship? Neurophysiology of spasms Rufinamide for the treatment of refractory epilepsy secondary to neuronal migration disorders Rufinamide efficacy and safety as adjunctive treatment in children with focal drug resistant epilepsy: the first Italian prospective study Epilepsy in patients with duplications of chromosome 14 harboring FOXG1. Video/EEG aspects of early-infantile epileptic encephalopathy with suppression-bursts (Ohtahara syndrome). Long-term follow-up in children with benign convulsions associated with gastroenteritis A novel mutation in the endosomal Na+/H+ exchanger NHE6 (SLC9A6) causes Christianson syndrome with electrical status epilepticus during slow-wave sleep (ESES). Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients PCDH19-related epilepsy in two mosaic male patients. Everolimus Alleviates Obstructive Hydrocephalus due to Subependymal Giant Cell Astrocytomas Clinical studies and anti-inflammatory mechanisms of treatments. Extending the use of stiripentol to other epileptic syndromes: a case of PCDH19-related epilepsy Paediatric anti-N-methyl-D-aspartate receptor encephalitis: The first Italian multicenter case series White matter disruption is associated with persistent seizures in tuberous sclerosis complex. Therapeutic approach to epileptic encephalopathies Dyskinesia as a new adverse effect of hormonal treatment in West syndrome. Definition and diagnostic criteria of sleep-related hypermotor epilepsy Hemiconvulsion-Hemiplegia-Epilepsy syndrome associated with inflammatory-degenerative hystopathological findings in child with congenital adrenal hyperplasia. Febrile infection-related epilepsy syndrome (FIRES) with super-refractory status epilepticus revealing autoimmune encephalitis due to GABAAR antibodies. Successful use of fenfluramine in nonconvulsive status epilepticus of Dravet syndrome Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study The phenotype of SCN8A developmental and epileptic encephalopathy Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study ATP1A3-related epileptic encephalopathy responding to ketogenic diet. Photosensitivity is an early marker of neuronal ceroid lipofuscinosis type 2 disease Pediatric status epilepticus: Identification of prognostic factors using the new ILAE classification after 5 years of follow-up PRRT2 is mutated in familial and non-familial benign infantile seizures Benign idiopathic partial epilepsies in infancy Ictal vomiting as a sign of temporal lobe epilepsy confirmed by stereo-EEG and surgical outcome Epileptic Spasms and Partial Seizures as a Single Ictal Event Acute intralesional recording in hypothalamic hamartoma: description of 4 cases. Alternating hemiplegia of childhood Focal seizures versus epileptic spasms in children with focal cortical dysplasia and epilepsy onset in the first year Reflex myoclonic epilepsy in infancy: a multicenter clinical study. Role of the Attachment Style in Determining the Association Between Headache Features and Psychological Symptoms in Migraine Children and Adolescents. An Analytical Observational Case-Control Study Maternal Alexithymia and Attachment Style: Which Relationship with Their Children's Headache Features and Psychological Profile? Cognitive development in females with PCDH19 gene-related epilepsy. Non-motor symptoms in movement disorders: more than meets the eye P016. Congenital ataxia, hemiplegic migraine due to a novel mutation of CACNA1A: a case report O016. Does migraine follow benign paroxysmal torticollis? Current role of perampanel in pediatric epilepsy. O019. Headache as an emergency in children and adolescents Midazolam vs diazepam in prolonged seizures in children: A pharmacoeconomic approach. Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia. Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 Mutations. Vigabatrin efficacy in GPR56-associated polymicrogyria: The role of GABAA receptor pathway

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