about
Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients.Incidence of epilepsy in extremely low-birthweight infants (<1,000 g): a population study of central and southern Sardinia.Idiopathic focal epilepsies: the "lost tribe".Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes.Early and effective treatment of KCNQ2 encephalopathy.The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy.Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy.Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.Pergolide improvement in neuroleptic-resistant Tourette cases: various mechanisms causing tics.Leigh-like neuroimaging features associated with new biallelic mutations in OPA1.Vertical extraventricular functional hemispherotomy: a new variant for hemispheric disconnection. Technical notes and results in three patients.Hypothermia for neonatal hypoxic-ischemic encephalopathy: may an early amplitude-integrated EEG improve the selection of candidates for cooling?Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsy.Progressive hemispheric shrinking in hemimegalencephaly: a possible role for seizure-related neuronal loss.Safety and efficacy of topiramate in neonates with hypoxic ischemic encephalopathy treated with hypothermia (NeoNATI): a feasibility study.CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of life.Ring chromosome 14 mosaicism: an unusual case associated with developmental delay and epilepsy, characterized by genome array-CGH.Megalencephaly, polymicrogyria, and hydrocephalus (MPPH) syndrome: a new case with syndactyly.Response to the letter to the Editor regarding "Leigh-like neuroimaging features associated with new bi-allelic mutations in OPA1".Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects.HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyondPrevalence of primary blepharospasm in Sardinia, Italy: A service-based surveyFamilial translocation t(3;10) (p26.3;p12.31) leading to trisomy 10p12.31-->pter and monosomy 3p26.3-->pter in seven membersCompression of superficial temporal arteries by a handmade device: a simple way to block or attenuate migraine attacks in children and adolescentsProgressive spastic paraplegia as a feature of tetrasomy 18pEarly infantile epileptic-dyskinetic encephalopathy due to biallelic PIGP mutationsLong-term efficacy of add-on stiripentol treatment in children, adolescents, and young adults with refractory epilepsies: A single center prospective observational study
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0001-8920-9078
@en
name
Tiziana Pisano
@ast
Tiziana Pisano
@en
Tiziana Pisano
@es
Tiziana Pisano
@nl
type
label
Tiziana Pisano
@ast
Tiziana Pisano
@en
Tiziana Pisano
@es
Tiziana Pisano
@nl
prefLabel
Tiziana Pisano
@ast
Tiziana Pisano
@en
Tiziana Pisano
@es
Tiziana Pisano
@nl
P106
P31
P496
0000-0001-8920-9078