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Stefano Sartori
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The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy
S Fehr, M Wilson, J Downs, S Williams, A Murgia, S Sartori, M Vecchi, ...
European Journal of Human Genetics 21 (3), 266-273, 2013
3272013
Antibiotic treatment for pyelonephritis in children: multicentre randomised controlled non-inferiority trial
G Montini, A Toffolo, P Zucchetta, R Dall'Amico, D Gobber, A Calderan, ...
Bmj 335 (7616), 386, 2007
2772007
Herpes simplex virus‐induced anti‐N‐methyl‐d‐aspartate receptor encephalitis: a systematic literature review with analysis of 43 cases
M Nosadini, SS Mohammad, F Corazza, EM Ruga, K Kothur, G Perilongo, ...
Developmental Medicine & Child Neurology 59 (8), 796-805, 2017
1872017
Use and safety of immunotherapeutic management of N-methyl-d-aspartate receptor antibody encephalitis: a meta-analysis
M Nosadini, M Eyre, E Molteni, T Thomas, SR Irani, J Dalmau, RC Dale, ...
JAMA neurology 78 (11), 1333-1344, 2021
1472021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
KM Johannesen, Y Liu, M Koko, CE Gjerulfsen, L Sonnenberg, J Schubert, ...
Brain 145 (9), 2991-3009, 2022
1172022
Comorbidity between headache and epilepsy in a pediatric headache center
I Toldo, E Perissinotto, F Menegazzo, C Boniver, S Sartori, L Salviati, ...
The journal of headache and pain 11, 235-240, 2010
1152010
Treatment of convulsive status epilepticus in childhood: Recommendations of the I talian L eague A gainst E pilepsy
G Capovilla, F Beccaria, E Beghi, F Minicucci, S Sartori, M Vecchi
Epilepsia 54, 23-34, 2013
1112013
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria
R Artuso, MA Mencarelli, R Polli, S Sartori, F Ariani, M Pollazzon, ...
Brain and Development 32 (1), 17-24, 2010
1112010
Plasma exchange in pediatric anti-NMDAR encephalitis: a systematic review
A Suppiej, M Nosadini, L Zuliani, MF Pelizza, I Toldo, C Bertossi, T Tison, ...
Brain and Development 38 (7), 613-622, 2016
882016
Management of antibody-mediated autoimmune encephalitis in adults and children: literature review and consensus-based practical recommendations
L Zuliani, M Nosadini, M Gastaldi, M Spatola, R Iorio, M Zoccarato, ...
Neurological Sciences 40, 2017-2030, 2019
782019
Characterization of intellectual disability and autism comorbidity through gene panel sequencing
MC Aspromonte, M Bellini, A Gasparini, M Carraro, E Bettella, R Polli, ...
Human mutation 40 (9), 1346-1363, 2019
782019
Pontocerebellar hypoplasia: clinical, pathologic, and genetic studies
D Cassandrini, R Biancheri, A Tessa, M Di Rocco, M Di Capua, C Bruno, ...
Neurology 75 (16), 1459-1464, 2010
722010
Paediatric anti-N-methyl-D-aspartate receptor encephalitis: the first Italian multicenter case series
S Sartori, M Nosadini, E Cesaroni, R Falsaperla, G Capovilla, F Beccaria, ...
European Journal of Paediatric Neurology 19 (4), 453-463, 2015
712015
First‐ever convulsive seizures in children presenting to the emergency department: risk factors for seizure recurrence and diagnosis of epilepsy
S Sartori, M Nosadini, G Tessarin, C Boniver, AC Frigo, I Toldo, S Bressan, ...
Developmental Medicine & Child Neurology 61 (1), 82-90, 2019
672019
Long-term neurocognitive outcome and quality of life in pediatric acute disseminated encephalomyelitis
A Suppiej, E Cainelli, G Casara, A Cappellari, M Nosadini, S Sartori
Pediatric Neurology 50 (4), 363-367, 2014
672014
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy
FM Santorelli, B Garavaglia, F Cardona, N Nardocci, BD Bernardina, ...
Orphanet Journal of Rare Diseases 8, 1-7, 2013
652013
Management of status epilepticus in adults. Position paper of the Italian League against Epilepsy
F Minicucci, M Ferlisi, F Brigo, O Mecarelli, S Meletti, U Aguglia, ...
Epilepsy & Behavior 102, 106675, 2020
642020
Neuroimaging changes in Menkes disease, part 1
R Manara, L D'Agata, MC Rocco, R Cusmai, E Freri, L Pinelli, F Darra, ...
American Journal of Neuroradiology 38 (10), 1850-1857, 2017
632017
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders
H Guo, E Bettella, PC Marcogliese, R Zhao, JC Andrews, TJ Nowakowski, ...
Nature communications 10 (1), 4679, 2019
612019
Serum and CSF neurofilament light chain levels in antibody-mediated encephalitis
S Mariotto, A Gajofatto, L Zuliani, M Zoccarato, M Gastaldi, D Franciotta, ...
Journal of neurology 266, 1643-1648, 2019
602019
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