CC and CXC chemokines are pivotal mediators of cerebral injury in ischaemic stroke

…, F Dallegri, A Quercioli, E Veneselli… - Thrombosis and …, 2011 - thieme-connect.com
The definition of ischaemic stroke has been recently updated as an acute episode of neurological
dysfunction caused by focal brain, spinal cord, or retinal ischaemia in the presence of …

Neuropsychological disorders related to interictal epileptic discharges during sleep in benign epilepsy of childhood with centrotemporal or Rolandic spikes

…, E De Negri, MG Calevo, E Veneselli… - … medicine and child …, 2001 - cambridge.org
Nine children (five males, four females; age range 6 years 1 month to 11 years 1 month)
affected by benign epilepsy of childhood with centrotemporal or Rolandic spikes (BECRS) with …

[HTML][HTML] Molecular genetics and interferon signature in the Italian Aicardi Goutières syndrome cohort: report of 12 new cases and literature review

…, E Veneselli, G Zorzi, B Garavaglia, E Fazzi… - Journal of Clinical …, 2019 - mdpi.com
Aicardi-Goutières syndrome (AGS) is a genetically determined early onset encephalopathy
characterized by cerebral calcification, leukodystrophy, and increased expression of …

Neuroblastoma with symptomatic spinal cord compression at diagnosis: treatment and results with 76 cases

…, P Pistamiglio, E Veneselli, E Viscardi… - Journal of clinical …, 2001 - ascopubs.org
PURPOSE: To report on the treatment of patients with newly diagnosed neuroblastoma
presenting with spinal cord compression (SCC). PATIENTS AND METHODS: Of 1,462 children …

A double‐blind, parallel, multicenter comparison of L‐acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boys

…, E Veneselli, E Cocchi, E Garbarino… - American Journal of …, 2008 - Wiley Online Library
Attention deficit hyperactivity disorder (ADHD) is a frequent behavioral problem in young boys
with fragile X syndrome (FXS), and its treatment is critical for improving social ability. The …

Long-term follow-up of neuroblastoma-associated opsoclonus-myoclonus-ataxia syndrome

…, WG Mitchell, M Pike, R Haupt, E Veneselli - …, 2009 - thieme-connect.com
Objective: The aim of this study is to describe the long-term neurological, neuropsychological
and neuroradiological sequelae and to determine prognostic factors for neurological …

Early‐onset cobalamin C/D deficiency: epilepsy and electroencephalographic features

…, MV Perrone, P Tortori‐Donati, E Veneselli - …, 2002 - Wiley Online Library
Purpose: To describe epilepsy and EEG findings in the early‐onset cobalamin (Cbl) C/D
deficiency, an inborn error of intracellular Cbl metabolism characterized by high plasma levels …

Video gesture analysis for autism spectrum disorder detection

…, J Podda, F Battaglia, E Veneselli… - 2018 24th …, 2018 - ieeexplore.ieee.org
Autism is a behavioral neurological disorder affecting a significant percentage of worldwide
population. It especially starts manifesting at very low ages, but it is difficult to early diagnose …

Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes

…, F Cogliati, MT Bonati, M Pintaudi, E Veneselli… - Neurogenetics, 2009 - Springer
It has been found that CDKL5 gene mutations are responsible for early-onset epilepsy and
drug resistance. We screened a population of 92 patients with classic/atypical Rett syndrome, …

Hypersomnia in the Prader Willi syndrome: clinical-electrophysiological features and underlying factors

…, L Nobili, F Ferrillo, C Livieri, E Veneselli… - Clinical …, 2001 - Elsevier
Objective: Excessive daytime sleepiness is a common symptom in Prader Willi syndrome (PWs).
Sleep disordered breathing (SDB) and narcoleptic traits such as REM sleep onsets (…