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An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy

Neurology, 2007-07, Vol.69 (3), p.250

2007

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Effectiveness and tolerability of Perampanel in children and adolescents with refractory epilepsies − an Italian observational multicenter study

Epilepsy research, 2016-11, Vol.127, p.93-100

2016

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Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype

Acta neurologica Scandinavica, 2005-04, Vol.111 (4), p.211-217

2005

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Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation

Neurology, 2011-03, Vol.76 (13), p.1173

2011

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Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations

Brain (London, England : 1878), 2006-07, Vol.129 (7), p.1892-1906

2006

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GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

Neurology, 2012-02, Vol.78 (8), p.557

2012

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LGI1 microdeletion in autosomal dominant lateral temporal epilepsy

Neurology, 2012-04, Vol.78 (17), p.1299

2012

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A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures

Neurology, 2007-06, Vol.68 (24), p.2150

2007

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Duchenne muscular dystrophy and epilepsy

Neuromuscular disorders : NMD, 2013-04, Vol.23 (4), p.313-315

2013

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Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5 -related epilepsy

European journal of paediatric neurology, 2016-01, Vol.20 (1), p.147-151

2016

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West syndrome associated with 14q12 duplications harboring FOXG1

Neurology, 2011-05, Vol.76 (18), p.1600

2011

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Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndrome

Epilepsy & behavior, 2011-07, Vol.21 (3), p.282-284

2011

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Familial mesial temporal lobe epilepsy (FMTLE): A clinical and genetic study of 15 Italian families

Journal of neurology, 2008, Vol.255 (1), p.16-23

2008

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Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases

Brain (London, England : 1878), 2004-06, Vol.127 (6), p.1343-1352

2004

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Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy

Neurology, 2006-10, Vol.67 (7), p.1230

2006

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Levetiracetam for cerebellar tremor in multiple sclerosis : An open-label pilot tolerability and efficacy study

Journal of neurology, 2006-06, Vol.253 (6), p.762-766

2006

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OP12 – 2577: Targeted resequencing in epileptic encephalopathies: diagnostic implications and genotype–phenotype correlations

European journal of paediatric neurology, 2015-05, Vol.19, p.S4-S5

2015

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Non-interventional surveillance study of adverse events in patients with epilepsy

Acta neurologica Scandinavica, 2011-07, Vol.124 (1), p.13-21

2011

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Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME

Neurology, 2003-04, Vol.60 (8), p.1381

2003

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First long-term experience with the orphan drug rufinamide in children with myoclonic-astatic epilepsy (Doose syndrome)

European journal of paediatric neurology, 2012-09, Vol.16 (5), p.459-463

2012

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Pediatric moyamoya disease and syndrome in Italy: Data from the Italian Society of Pediatric Neurology multicentric retrospective study

European journal of paediatric neurology, 2017-06, Vol.21, p.e151-e151

2017

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Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis

Epilepsy research, 2010-05, Vol.89 (2), p.286-294

2010

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P93 – 2953: Identification of a new mutation of the SCL1A gene in a patient with GLUT1-DS

European journal of paediatric neurology, 2015-05, Vol.19, p.S120-S120

2015

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3.070 AUTOSOMAL DOMINANT CORTICAL MYOCLONUS AND EPILEPSY (ADCME) - NEW MUTATION IN POLISH FAMILY?

Parkinsonism & related disorders, 2012, Vol.18, p.S186-S186

2012

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Epileptic seizures in multiple sclerosis: clinical and EEG correlations

Neurological sciences, 2003-12, Vol.24 (5), p.322-328

2003

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An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy

Effectiveness and tolerability of Perampanel in children and adolescents with refractory epilepsies − an Italian observational multicenter study

Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype

Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations

GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy

A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures

Duchenne muscular dystrophy and epilepsy

Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5 -related epilepsy

West syndrome associated with 14q12 duplications harboring FOXG1

Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndrome

Familial mesial temporal lobe epilepsy (FMTLE): A clinical and genetic study of 15 Italian families

Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases

Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy

Levetiracetam for cerebellar tremor in multiple sclerosis : An open-label pilot tolerability and efficacy study

OP12 – 2577: Targeted resequencing in epileptic encephalopathies: diagnostic implications and genotype–phenotype correlations

Non-interventional surveillance study of adverse events in patients with epilepsy

Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME

First long-term experience with the orphan drug rufinamide in children with myoclonic-astatic epilepsy (Doose syndrome)

Pediatric moyamoya disease and syndrome in Italy: Data from the Italian Society of Pediatric Neurology multicentric retrospective study

Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis

P93 – 2953: Identification of a new mutation of the SCL1A gene in a patient with GLUT1-DS

3.070 AUTOSOMAL DOMINANT CORTICAL MYOCLONUS AND EPILEPSY (ADCME) - NEW MUTATION IN POLISH FAMILY?

Epileptic seizures in multiple sclerosis: clinical and EEG correlations

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