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 …
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 …
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 …
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 …
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 …
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 …
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 …
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 …
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, …
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 (…
Sleep disordered breathing (SDB) and narcoleptic traits such as REM sleep onsets (…