About: Bernardo Dalla Bernardina

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researcher

Attributes	Values
rdf:type	Item
description	researcher (en) wetenschapper (nl) дослідник (uk) изилдөөчү (ky)
rdfs:label	Bernardo Dalla Bernardina (en) Bernardo Dalla Bernardina (ast)
skos:prefLabel	Bernardo Dalla Bernardina (en) Bernardo Dalla Bernardina (ast)
name	Bernardo Dalla Bernardina (en) Bernardo Dalla Bernardina (ast)
instance of	wds:Q114340198-E721DA84-BCFD-4DC9-BE0A-5D2D3C6E11E6
instance of	Homo sapiens
skos:altLabel	Bernadina, Bernardo Dalla (en) Dalla Bernadina, Bernardo (en)
occupation	wds:Q114340198-D7872226-E209-44F8-BE29-DA399D40E8E4
VIAF ID	wds:Q114340198-d329df0b-4d1b-1701-76ea-c2766bd57f13
Library of Congress authority ID	wds:Q114340198-eb37b4e0-45e5-6882-a2a0-7c5f53d8b33c
SHARE Catalogue author ID	wds:Q114340198-C62B3559-9B43-4418-A804-4BEE3314364C
National Library of Israel J9U ID	wds:Q114340198-936C5D1A-2848-4529-B8AD-56150B99B153
VIAF ID	http://viaf.org/viaf/39691556
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2007184303
occupation	researcher
VIAF ID	39691556
Library of Congress authority ID	n2007184303
SHARE Catalogue author ID	286385
National Library of Israel J9U ID	987007325075905171
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q114340198
is author of	Restless legs syndrome and attention-deficit/hyperactivity disorder: a review of the literature Sleep disturbances and serum ferritin levels in children with attention-deficit/hyperactivity disorder. Attention-deficit/hyperactivity disorder, Tourette's syndrome, and restless legs syndrome: the iron hypothesis Lack of SCN1A mutations in familial febrile seizures Attention-deficit/hyperactivity disorder (ADHD) and obesity: a systematic review of the literature Association between symptoms of attention-deficit/hyperactivity disorder and bulimic behaviors in a clinical sample of severely obese adolescents. Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy Attention-deficit/hyperactivity disorder (ADHD) and binge eating 4p- Syndrome: A Chromosomal Disorder Associated with a Particular EEG Pattern No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1. Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations. Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations Refining the phenotype associated with MEF2C haploinsufficiency. Parent reports of sleep/alertness problems and ADHD symptoms in a sample of obese adolescents. The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype Xp22.3 genomic deletions involving the CDKL5 gene in girls with early onset epileptic encephalopathy Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria. Pathogenic role of the X-linked cyclin-dependent kinase-like 5 and aristaless-related homeobox genes in epileptic encephalopathy of unknown etiology with onset in the first year of life. Periventricular heterotopia in fragile X syndrome. A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures Oxidative stress-related biomarkers in autism: systematic review and meta-analyses Epilepsy and EEG findings in males with fragile X syndrome. Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance. PRRT2 mutations are the major cause of benign familial infantile seizures. Polygraphic study of dyssynergia cerebellaris myoclonica (Ramsay-Hunt syndrome) and of the intention myoclonus (Lance-Adams syndrome) during sleep. Epileptic spasms in clusters without hypsarrhythmia in infancy. Benign myoclonus of early infancy or benign non-epileptic infantile spasms. Rasmussen's syndrome: longitudinal EEG study from the first seizure to epilepsia partialis continua. 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 Diagnostic imaging in 13 cases of Rasmussen's encephalitis: can early MRI suggest the diagnosis? Experience with immunomodulatory treatments in Rasmussen's encephalitis Syndrome with periodic central apnea during wakefulness and transient disturbances of consciousness ("syncopes" of respiratory arrest) Does excessive daytime sleepiness contribute to explaining the association between obesity and ADHD symptoms? Brain iron levels in attention-deficit/hyperactivity disorder: A pilot MRI study Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families. Early-onset absence epilepsy and paroxysmal dyskinesia The electrical status epilepticus syndrome Familial Ohtahara syndrome due to a novel ARX gene mutation Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases. Electroencephalographic characteristics of Dravet syndrome Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients Acute measles encephalitis of the delayed type in an immunosuppressed child Recommendations of the Italian League against Epilepsy working group on generic products of antiepileptic drugs The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: an Italian consensus. Microgyria associated with Sturge-Weber angiomatosis. Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locus. Infantile spasms: toward a selective diagnostic and therapeutic approach Electroclinical findings in four patients with karyotype 47,XYY. Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients. Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children Severe infant myoclonic epilepsy (author's transl) Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR. Paediatric anti-N-methyl-D-aspartate receptor encephalitis: The first Italian multicenter case series Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15). Early myoclonic epileptic encephalopathy (E.M.E.E.). Infantile spams without hypsarrhythmia: a study of 16 cases. The relationship between body size and depression symptoms in adolescents. Rolandic spikes in children with and without epilepsy. (20 subjects polygraphically studied during sleep) The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy. Restless legs syndrome triggered by heart surgery. Status epilepticus in benign rolandic epilepsy manifesting as anterior operculum syndrome. The visual system in eyelid myoclonia with absences Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20. A study of 63 cases with eyelid myoclonia with or without absences: type of seizure or an epileptic syndrome? Benign focal epilepsy and "electrical status epilepticus" during sleep (author's transl) Biotin-responsive infantile encephalopathy: EEG-polygraphic study of a case. Symmetrical bithalamic hyperdensities in asphyxiated full-term newborns: an early indicator of status marmoratus Tuberous sclerosis and Down syndrome: a casual association? Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. Clinical dissection of early onset absence epilepsy in children and prognostic implications.

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