Antonietta Coppola
Antonietta Coppola
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Recurrent rearrangements of chromosome 1q21. 1 and variable pediatric phenotypes
HC Mefford, AJ Sharp, C Baker, A Itsara, Z Jiang, K Buysse, S Huang, ...
New England Journal of Medicine 359 (16), 1685-1699, 2008
Characterization of a recurrent 15q24 microdeletion syndrome
AJ Sharp, RR Selzer, JA Veltman, S Gimelli, G Gimelli, P Striano, ...
Human molecular genetics 16 (5), 567-572, 2007
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy
P Striano, A Coppola, M Pezzella, C Ciampa, N Specchio, F Ragona, ...
Neurology 69 (3), 250-254, 2007
A pulse rapamycin therapy for infantile spasms and associated cognitive decline
E Raffo, A Coppola, T Ono, SW Briggs, AS Galanopoulou
Neurobiology of disease 43 (2), 322-329, 2011
CHD2 variants are a risk factor for photosensitivity in epilepsy
EC Galizia, CT Myers, C Leu, CGF De Kovel, T Afrikanova, ...
Brain 138 (5), 1198-1208, 2015
Evidence for mTOR pathway activation in a spectrum of epilepsy-associated pathologies
J Liu, C Reeves, Z Michalak, A Coppola, B Diehl, SM Sisodiya, M Thom
Acta neuropathologica communications 2 (1), 1-13, 2014
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization
P Striano, A Coppola, R Paravidino, M Malacarne, S Gimelli, A Robbiano, ...
Archives of neurology 69 (3), 322-330, 2012
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome)
P Striano, V Sofia, G Capovilla, G Rubboli, C Di Bonaventura, A Coppola, ...
Epilepsia 49 (3), 425-430, 2008
The challenges of treating epilepsy with 25 antiepileptic drugs
L Santulli, A Coppola, S Balestrini, S Striano
Pharmacological research 107, 211-219, 2016
Familial mesial temporal lobe epilepsy (FMTLE)
P Striano, A Gambardella, A Coppola, C Di Bonaventura, G Bovo, E Diani, ...
Journal of neurology 255 (1), 16-23, 2008
exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy
ST Mĝller RS, Weber YG, Klitten LL, Trucks H, Muhle H, Kunz WS, Mefford HC ...
Epilepsia 2 (54), 256-264, 2013
Reflex seizures and reflex epilepsies: old models for understanding mechanisms of epileptogenesis
S Striano, A Coppola, L del Gaudio, P Striano
Epilepsy research 100 (1-2), 1-11, 2012
West syndrome associated with 14q12 duplications harboring FOXG1
P Striano, R Paravidino, F Sicca, P Chiurazzi, S Gimelli, A Coppola, ...
Neurology 76 (18), 1600-1602, 2011
Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation
P Striano, G Busolin, L Santulli, E Leonardi, A Coppola, L Vitiello, L Rigon, ...
Neurology 76 (13), 1173-1176, 2011
Effectiveness of antiepileptic therapy in patients with PCDH19 mutations
J Lotte, T Bast, P Borusiak, A Coppola, JH Cross, P Dimova, A Fogarasi, ...
Seizure 35, 106-110, 2016
Animal models
A Coppola, SL Moshé
Handbook of clinical neurology 107, 63-98, 2012
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: five new cases
P Striano, M Malacarne, S Cavani, M Pierluigi, R Rinaldi, ML Cavaliere, ...
American journal of medical genetics Part A 140 (18), 1944-1949, 2006
Natural history and long‐term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy
A Coppola, L Santulli, L Del Gaudio, C Minetti, S Striano, F Zara, P Striano
Epilepsia 52 (7), 1245-1250, 2011
Dramatic response to levetiracetam in post-ischaemic Holmes’ tremor
P Striano, A Elefante, A Coppola, F Tortora, F Zara, C Minetti, S Striano
Journal of Neurology, Neurosurgery & Psychiatry 78 (4), 438-439, 2007
Levetiracetam for cerebellar tremor in multiple sclerosis
P Striano, A Coppola, G Vacca, F Zara, VB Morra, G Orefice, S Striano
Journal of neurology 253 (6), 762-766, 2006
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Artikelen 1–20