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Comorbidities in patients with epilepsy: Frequency, mechanisms and effects on long‐term outcome

Epilepsia (Copenhagen), 2021-10, Vol.62 (10), p.2395-2404

2021

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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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Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome

Neurology, 2005-01, Vol.64 (2), p.254

2005

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Diagnostic imaging in 13 cases of Rasmussen's encephalitis: Can early MRI suggest the diagnosis?

Neuroradiology, 2003-03, Vol.45 (3), p.171-183

2003

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119. Could focal epilepsy be part of a phenotype associated with Tourette’s syndrome?

Epilepsy & behavior, 2010-04, Vol.17 (4), p.614-615

2010

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Anakinra usage in febrile infection related epilepsy syndrome: an international cohort

Annals of clinical and translational neurology, 2020-12, Vol.7 (12), p.2467-2474

2020

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Prevalence of Anti‐cardiolipin, Anti‐β2 Glycoprotein I, and Anti‐prothrombin Antibodies in Young Patients with Epilepsy

Epilepsia (Copenhagen), 2002-01, Vol.43 (1), p.52-59

2002

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Benign Partial Epilepsies of Adolescence: A Report of 37 New Cases

Epilepsia (Copenhagen), 2001-12, Vol.42 (12), p.1549-1552

2001

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A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome)

Epilepsia (Copenhagen), 2008-03, Vol.49 (3), p.425-430

2008

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Novel mutations of ubiquitin protein ligase 3A gene in Italian patients with Angelman syndrome

Human mutation, 2000-04, Vol.15 (4), p.387-387

2000

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Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial

Epilepsy research, 2002-03, Vol.49 (1), p.45-48

2002

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ILAE Classification of Epilepsies: Its Applicability and Practical Value of Different Diagnostic Categories

Epilepsia (Copenhagen), 1996-11, Vol.37 (11), p.1051-1059

Osservatorio Regionale per L'Epilessia (OREp), Lombardy

1996

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Treatment of first tonic–clonic seizure does not affect mortality: long-term follow-up of a randomised clinical trial

Journal of neurology, neurosurgery and psychiatry, 2011-08, Vol.82 (8), p.924-927

2011

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Prevalence of Anti‐cardiolipin, Anti‐β 2 Glycoprotein I, and Anti‐prothrombin Antibodies in Young Patients with Epilepsy

Epilepsia (Copenhagen), 2002-01, Vol.43 (1), p.52-59

2002

Volltextzugriff (PDF)

A new Italian instrument for the assessment of irritability in patients with epilepsy

Epilepsy & behavior, 2011-07, Vol.21 (3), p.275-281

2011

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Inter-rater reliability of the EEG reading in patients with childhood idiopathic epilepsy

Epilepsy research, 2005-08, Vol.66 (1), p.195-198

2005

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Does the Co-occurrence of FGFR3 Gene Mutation in Hypochondroplasia, Medial Temporal Lobe Dysgenesis, and Focal Epilepsy Suggest a Syndrome?

Pediatric neurology, 2014-04, Vol.50 (4), p.427-430

2014

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The Contribution of Tertiary Centers to the Quality of the Diagnosis and Treatment of Epilepsy

Epilepsia (Copenhagen), 1997-12, Vol.38 (12), p.1338-1343

Osservatorio Regionale per l'Epilessia (OREp), Lombardy

1997

Volltextzugriff (PDF)

Electrical status epilepticus on eye closure: a case report

Neurophysiologie clinique, 1992-09, Vol.22 (4), p.281-286

1992

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Vaccination and Occurrence of Seizures in SCN1A Mutation–Positive Patients: A Multicenter Italian Study

Pediatric neurology, 2014-03, Vol.50 (3), p.228-232

2014

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Congenital muscular dystrophy with muscle inflammation alpha dystroglycan glycosylation defect and no mutation in FKRP gene

Journal of the neurological sciences, 2006-04, Vol.243 (1), p.47-51

2006

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Infantile spasms combined with partial seizures: electroclinical study of eleven cases

Italian journal of neurological sciences, 1994-12, Vol.15 (9), p.463-471

1994

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No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy

Epilepsy research, 2003-03, Vol.53 (3), p.196-200

2003

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Seizure and EEG Patterns in Angelman's Syndrome

Journal of child neurology, 1995-11, Vol.10 (6), p.467-471

1995

Volltextzugriff (PDF)

Family study of epilepsy in first degree relatives: data from the Italian Episcreen Study

Seizure (London, England), 2003-06, Vol.12 (4), p.203-210

2003

Volltextzugriff (PDF)

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Comorbidities in patients with epilepsy: Frequency, mechanisms and effects on long‐term outcome

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

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome

Diagnostic imaging in 13 cases of Rasmussen's encephalitis: Can early MRI suggest the diagnosis?

119. Could focal epilepsy be part of a phenotype associated with Tourette’s syndrome?

Anakinra usage in febrile infection related epilepsy syndrome: an international cohort

Prevalence of Anti‐cardiolipin, Anti‐β2 Glycoprotein I, and Anti‐prothrombin Antibodies in Young Patients with Epilepsy

Benign Partial Epilepsies of Adolescence: A Report of 37 New Cases

A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome)

Novel mutations of ubiquitin protein ligase 3A gene in Italian patients with Angelman syndrome

Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial

ILAE Classification of Epilepsies: Its Applicability and Practical Value of Different Diagnostic Categories

Treatment of first tonic–clonic seizure does not affect mortality: long-term follow-up of a randomised clinical trial

Prevalence of Anti‐cardiolipin, Anti‐β 2 Glycoprotein I, and Anti‐prothrombin Antibodies in Young Patients with Epilepsy

A new Italian instrument for the assessment of irritability in patients with epilepsy

Inter-rater reliability of the EEG reading in patients with childhood idiopathic epilepsy

Does the Co-occurrence of FGFR3 Gene Mutation in Hypochondroplasia, Medial Temporal Lobe Dysgenesis, and Focal Epilepsy Suggest a Syndrome?

The Contribution of Tertiary Centers to the Quality of the Diagnosis and Treatment of Epilepsy

Electrical status epilepticus on eye closure: a case report

Vaccination and Occurrence of Seizures in SCN1A Mutation–Positive Patients: A Multicenter Italian Study

Congenital muscular dystrophy with muscle inflammation alpha dystroglycan glycosylation defect and no mutation in FKRP gene

Infantile spasms combined with partial seizures: electroclinical study of eleven cases

No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy

Seizure and EEG Patterns in Angelman's Syndrome

Family study of epilepsy in first degree relatives: data from the Italian Episcreen Study

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