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Pubblicazioni
BRAIN & DEVELOPMENT
Rivista
Codice:
E024690
ISSN:
0387-7604
Dati Generali
Dati Generali
Pubblicazioni (22)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
A correlated fluctuation of language and EEG abnormalities in a case of the Landau-Kleffner syndrome.
Articolo
A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation and dysmorphisms.
Articolo
A de novo ZMYM2 gene variant associated to a Rett-like phenotype: Case report of a new phenotype and review of the literature
Articolo
A novel variant in NEUROD2 in a patient with Rett-like phenotype points to Glu130 codon as a mutational hotspot
Articolo
Auditory attention at the onset of West syndrome: correlation with EEG patternsand visual function.
Articolo
Clinical and stabilometric monitoring in a case of cerebellar atrophy with vitamin E deficiency
Articolo
Delayed appearance of interictal EEG abnormalities in early onset childhood epilepsy with occipital paroxysms.
Articolo
Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients.
Articolo
Electroclinical findings in four patients with karyotype 47,XYY
Articolo
Glucose transporter type 1 deficiency: ketogenic diet in three patients with atypical phenotype
Articolo
Ictal EEG patterns in epilepsy with centro-temporal spikes.
Articolo
Long-term follow-up of an adolescent who had bilateral striatal necrosis secondary to Mycoplasma pneumoniae infection
Articolo
Long-term follow-up of an adolescent who had bilateral striatal necrosis secondary to Mycoplasma pneumoniae infection.
Articolo
Mutational scanning of potassium, sodium and chloride ion channels in malignant migrating partial seizures in infancy
Articolo
Mutations in α- and β-tubulin encoding genes: implications in brain malformations
Articolo
Myoclonic status epilepticus following high-dosage lamotrigine therapy
Articolo
Psychopathology in children and adolescents with Tourette's Syndrome: a controlled study.
Articolo
Ring chromosome 9: an atypical case.
Articolo
Schuurs-Hoeijmakers syndrome: Severe expression of the recurrent PACS1 c.607C>T mutation
Articolo
Sleep disturbances in visually impaired toddlers.
Articolo
The Rorschach test and Gilles de la Tourette's syndrome: A pilot case-control study.
Articolo
Visual-perceptual impairment in children with periventricular leukomalacia
Articolo
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