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Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome

Brain & development (Tokyo. 1979), 2019-06, Vol.41 (6), p.522-530

2019

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Somatic and germline mosaicisms in Severe Myoclonic Epilepsy of Infancy

Biochemical and biophysical research communications, 2006-03, Vol.341 (2), p.489-493

2006

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Severe Epilepsy in X‐Linked Creatine Transporter Defect (CRTR‐D)

Epilepsia (Copenhagen), 2007-06, Vol.48 (6), p.1211-1213

2007

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Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases

American journal of medical genetics. Part A, 2006-09, Vol.140A (18), p.1944-1949

2006

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Novel mutations in CLN8 in italian variant late infantile neuronal ceroid lipofuscinosis : another genetic hit in the Mediterranean

Neurogenetics, 2006-05, Vol.7 (2), p.111-117

2006

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Lack of SCN1A Mutations in Familial Febrile Seizures

Epilepsia (Copenhagen), 2002-05, Vol.43 (5), p.559-562

2002

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Epilepsy associated with infantile hemiparesis : predictors of long-term evolution

Brain & development (Tokyo. 1979), 2001-03, Vol.23 (1), p.12-17

2001

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Treatment of electrical status epilepticus by short diazepam (DZP) cycles after DZP rectal bolus test

Brain & development (Tokyo. 1979), 1995-09, Vol.17 (5), p.330-333

1995

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Clinical and electroencephalographic features in patients with CDKL5 mutations: Two new Italian cases and review of the literature

Epilepsy & behavior, 2008-02, Vol.12 (2), p.326-331

2008

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Early classification of childhood focal idiopathic epilepsies: Is it possible at the first seizure?

European journal of paediatric neurology, 2014-05, Vol.18 (3), p.376-380

2014

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Epilepsy associated with supratentorial brain tumors under 3 years of life

Epilepsy research, 2009-12, Vol.87 (2), p.184-189

2009

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6q Terminal Deletion Syndrome Associated with a Distinctive EEG and Clinical Pattern: A Report of Five Cases

Epilepsia (Copenhagen), 2006-05, Vol.47 (5), p.830-838

2006

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Occlusion of unilateral carotid artery in Down syndrome

Brain & development (Tokyo. 1979), 1996, Vol.18 (1), p.81-83

1996

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Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations

Epilepsy & behavior, 2007-02, Vol.10 (1), p.187-191

2007

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Intractable Epilepsy Secondary to Cyclosporine Toxicity in Children Undergoing Allogeneic Hematopoietic Bone Marrow Transplantation

Journal of child neurology, 2006-10, Vol.21 (10), p.861-866

2006

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Linkage Analysis and Disease Models in Benign Familial Infantile Seizures: A Study of 16 Families

Epilepsia (Copenhagen), 2006-06, Vol.47 (6), p.1029-1034

2006

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Hashimoto's encephalopathy with selective involvement of the nucleus accumbens: a case report

Neuropediatrics, 2005-06, Vol.36 (3), p.218

2005

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Malignant migrating partial seizures in infancy

Epilepsy research, 2001-07, Vol.46 (1), p.27-32

2001

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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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Benign Parasomnias and Nocturnal Frontal Epilepsy: Differential Diagnosis in a Case Report

Journal of child neurology, 2001-08, Vol.16 (8), p.628-631

2001

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Early-onset progressive encephalophathy with migrant, continuous myoclonus

Child's nervous system, 1996-05, Vol.12 (5), p.254-261

1996

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Benzodiazepine (BDZ) treatment of benign childhood epilepsy with centrotemporal spikes (BECCT)

Brain & development (Tokyo. 1979), 1997-11, Vol.19 (7), p.506-506

1997

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SPECT and epilepsy with continuous spike waves during slow-wave sleep

Child's nervous system, 1995-03, Vol.11 (3), p.154-160

1995

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Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome

Somatic and germline mosaicisms in Severe Myoclonic Epilepsy of Infancy

Brain MRI Findings in Severe Myoclonic Epilepsy in Infancy and Genotype–Phenotype Correlations

Severe Epilepsy in X‐Linked Creatine Transporter Defect (CRTR‐D)

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases

Novel mutations in CLN8 in italian variant late infantile neuronal ceroid lipofuscinosis : another genetic hit in the Mediterranean

Lack of SCN1A Mutations in Familial Febrile Seizures

Epilepsy associated with infantile hemiparesis : predictors of long-term evolution

Treatment of electrical status epilepticus by short diazepam (DZP) cycles after DZP rectal bolus test

Clinical and electroencephalographic features in patients with CDKL5 mutations: Two new Italian cases and review of the literature

Early classification of childhood focal idiopathic epilepsies: Is it possible at the first seizure?

Epilepsy associated with supratentorial brain tumors under 3 years of life

6q Terminal Deletion Syndrome Associated with a Distinctive EEG and Clinical Pattern: A Report of Five Cases

Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations

Occlusion of unilateral carotid artery in Down syndrome

Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations

Intractable Epilepsy Secondary to Cyclosporine Toxicity in Children Undergoing Allogeneic Hematopoietic Bone Marrow Transplantation

Linkage Analysis and Disease Models in Benign Familial Infantile Seizures: A Study of 16 Families

Hashimoto's encephalopathy with selective involvement of the nucleus accumbens: a case report

Malignant migrating partial seizures in infancy

No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy

Benign Parasomnias and Nocturnal Frontal Epilepsy: Differential Diagnosis in a Case Report

Early-onset progressive encephalophathy with migrant, continuous myoclonus

Benzodiazepine (BDZ) treatment of benign childhood epilepsy with centrotemporal spikes (BECCT)

SPECT and epilepsy with continuous spike waves during slow-wave sleep

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