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Pierangelo Veggiotti
Pierangelo Veggiotti
Email verificata su unipv.it
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Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group
EH Kossoff, BA Zupec‐Kania, PE Amark, KR Ballaban‐Gil, ...
Epilepsia 50 (2), 304-317, 2009
7232009
Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group
EH Kossoff, BA Zupec‐Kania, S Auvin, KR Ballaban‐Gil, ...
Epilepsia open 3 (2), 175-192, 2018
5632018
Neurofunctional correlates of vulnerability to psychosis: a systematic review and meta-analysis
P Fusar-Poli, J Perez, M Broome, S Borgwardt, A Placentino, E Caverzasi, ...
Neuroscience & Biobehavioral Reviews 31 (4), 465-484, 2007
3772007
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations
E Parrini, A Ramazzotti, WB Dobyns, D Mei, F Moro, P Veggiotti, C Marini, ...
Brain 129 (7), 1892-1906, 2006
3722006
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy
R Nabbout, E Gennaro, B Dalla Bernardina, O Dulac, F Madia, E Bertini, ...
Neurology 60 (12), 1961-1967, 2003
3292003
The ketogenic diet: from molecular mechanisms to clinical effects
J Freeman, P Veggiotti, G Lanzi, A Tagliabue, E Perucca
Epilepsy Res 68 (2), 145-80, 2006
3062006
GLUT1 deficiency syndrome 2013: current state of the art
V De Giorgis, P Veggiotti
Seizure 22 (10), 803-811, 2013
2172013
Post-operative benefits of animal-assisted therapy in pediatric surgery: A randomised study
V Calcaterra, P Veggiotti, C Palestrini, V De Giorgis, R Raschetti, ...
PloS one 10 (6), e0125813, 2015
2132015
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome
VL Sheen, A Jansen, MH Chen, E Parrini, T Morgan, R Ravenscroft, ...
Neurology 64 (2), 254-262, 2005
2102005
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ...
Nature communications 10 (1), 3094, 2019
1952019
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group
J Klepper, C Akman, M Armeno, S Auvin, M Cervenka, HJ Cross, ...
Epilepsia open 5 (3), 354-365, 2020
1842020
The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an Italian multicentric experience
G Coppola, P Veggiotti, R Cusmai, S Bertoli, S Cardinali, C Dionisi-Vici, ...
Epilepsy research 48 (3), 221-227, 2002
1832002
Evidence of thalamic gray matter loss in pediatric multiple sclerosis
S Mesaros, MA Rocca, M Absinta, A Ghezzi, N Milani, L Moiola, ...
Neurology 70 (13_part_2), 1107-1112, 2008
1752008
Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial
G Coppola, G Capovilla, A Montagnini, A Romeo, M Spanò, G Tortorella, ...
Epilepsy research 49 (1), 45-48, 2002
1532002
Treatment of electrical status epilepticus in sleep: a pooled analysis of 575 cases
B Van Den Munckhof, V Van Dee, L Sagi, RH Caraballo, P Veggiotti, ...
Epilepsia 56 (11), 1738-1746, 2015
1522015
The phenotype of SCN8A developmental and epileptic encephalopathy
E Gardella, C Marini, M Trivisano, MP Fitzgerald, M Alber, KB Howell, ...
Neurology 91 (12), e1112-e1124, 2018
1502018
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance
F Zara, N Specchio, P Striano, A Robbiano, E Gennaro, R Paravidino, ...
Epilepsia 54 (3), 425-436, 2013
1492013
Mutations in PROSC disrupt cellular pyridoxal phosphate homeostasis and cause vitamin-B6-dependent epilepsy
N Darin, E Reid, L Prunetti, L Samuelsson, RA Husain, M Wilson, ...
The American Journal of Human Genetics 99 (6), 1325-1337, 2016
1482016
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients
F Ragona, T Granata, BD Bernardina, F Offredi, F Darra, D Battaglia, ...
Epilepsia 52 (2), 386-392, 2011
1482011
Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies
S Masnada, UBS Hedrich, E Gardella, J Schubert, C Kaiwar, EW Klee, ...
Brain 140 (9), 2337-2354, 2017
1442017
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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