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Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology

Lancet neurology, 2009, Vol.8 (1), p.82-93

2009

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Sequential MR Angiography in Childhood Primary Angiitis of the CNS

Pediatric neurology, 2013-08, Vol.49 (2), p.127-129

2013

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Haemorheological disturbances and possibility of their correction in cerebrovascular diseases

Journal des maladies vasculaires, 1999-05, Vol.24 (2), p.110-116

1999

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Long-lasting antinociceptive spinal effects in primates of the novel nociceptin/orphanin FQ receptor agonist UFP-112

Pain (Amsterdam), 2010-01, Vol.148 (1), p.107-113

2010

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Efficacy and safety of ketamine in refractory status epilepticus in children

Neurology, 2012-12, Vol.79 (24), p.2355-2358

2012

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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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PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures

Neurology, 2012-11, Vol.79 (21), p.2104-2108

2012

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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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Additive effect of DNAJC30 and NDUFA9 mutations causing Leigh syndrome

Journal of neurology, 2023-06, Vol.270 (6), p.3266-3269

2023

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GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

Neurology, 2012-02, Vol.78 (8), p.557-562

2012

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Red Flags for early referral of people with symptoms suggestive of narcolepsy: a report from a national multidisciplinary panel

Neurological sciences, 2019-03, Vol.40 (3), p.447-456

2019

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Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus

Neurology, 2007-07, Vol.69 (5), p.427-433

2007

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7T Epilepsy Task Force Consensus Recommendations on the Use of 7T MRI in Clinical Practice

Neurology, 2021-02, Vol.96 (7), p.327-341

2021

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Reorganisation of the somatosensory system after early brain damage

Clinical neurophysiology, 2007-05, Vol.118 (5), p.1110-1121

2007

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Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2 , in perisylvian polymicrogyria: a next-generation sequencing study

Lancet neurology, 2015-12, Vol.14 (12), p.1182-1195

2015

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Shaping the future of European epilepsy research: Final meeting report from EPICLUSTER

Epilepsy research, 2023-01, Vol.189, p.107068-107068, Article 107068

2023

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Timing of antiepileptic drug withdrawal and long-term seizure outcome after paediatric epilepsy surgery (TimeToStop): a retrospective observational study

Lancet neurology, 2012-09, Vol.11 (9), p.784-791

2012

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Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

Neurology, 2003-06, Vol.60 (12), p.1961-1967

2003

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P850: Electrophysiological pattern in GLUT1 deficiency syndrome (A275T mutation)

Clinical neurophysiology, 2014-06, Vol.125, p.S269-S269

2014

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Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy

Neurology, 2013-03, Vol.80 (12), p.1078-1085

2013

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Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria

Neurology, 2014-03, Vol.82 (12), p.1068-1075

2014

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Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome

Neurology, 2005-01, Vol.64 (2), p.254-262

2005

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Multilobar polymicrogyria, intractable drop attack seizures, and sleep-related electrical status epilepticus

Neurology, 1998-08, Vol.51 (2), p.504-512

1998

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Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2

Brain (London, England : 1878), 2013-04, Vol.136 (Pt 4), p.1155-1160

2013

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Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology

Sequential MR Angiography in Childhood Primary Angiitis of the CNS

Haemorheological disturbances and possibility of their correction in cerebrovascular diseases

Long-lasting antinociceptive spinal effects in primates of the novel nociceptin/orphanin FQ receptor agonist UFP-112

Efficacy and safety of ketamine in refractory status epilepticus in children

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

PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations

Additive effect of DNAJC30 and NDUFA9 mutations causing Leigh syndrome

GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

Red Flags for early referral of people with symptoms suggestive of narcolepsy: a report from a national multidisciplinary panel

Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus

7T Epilepsy Task Force Consensus Recommendations on the Use of 7T MRI in Clinical Practice

Reorganisation of the somatosensory system after early brain damage

Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2 , in perisylvian polymicrogyria: a next-generation sequencing study

Shaping the future of European epilepsy research: Final meeting report from EPICLUSTER

Timing of antiepileptic drug withdrawal and long-term seizure outcome after paediatric epilepsy surgery (TimeToStop): a retrospective observational study

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

P850: Electrophysiological pattern in GLUT1 deficiency syndrome (A275T mutation)

Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy

Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome

Multilobar polymicrogyria, intractable drop attack seizures, and sleep-related electrical status epilepticus

Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2

Effectiveness of antiepileptic therapy in patients with PCDH19 mutations

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