Accorsi, P.

Developmental Delay, Tremors, and EEG Abnormalities: A Case of KCTD7 Gene Mutation

Acquaviva, Cécile

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Addor, M. C.

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Agati, Raffaele

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Altafaj, X.

Grin1-Related Early Onset Encephalopathy: A Distinct NMDA Receptor Dysfunction

Angelo, Russo

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Antonella, Boni

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Antonella, Pini

Ceroid Lipofuscinosis Type 2 (CLN-2): What Are the Early Neurophysiological Signs?

Antonio, V. San

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

Antonio-Arce, Victoria San

Diagnostic Exome Sequencing in Patients with Epilepsy

Aparicio, Javier

Diagnostic Exome Sequencing in Patients with Epilepsy

Armstrong, J.

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

Grin1-Related Early Onset Encephalopathy: A Distinct NMDA Receptor Dysfunction

Armstrong, Judith

Diagnostic Exome Sequencing in Patients with Epilepsy

Arnold, Susan

Lafora Disease: A Perspective in Molecular Mechanism and Pathology

Arossa, A.

Targeted Therapy in Channelopathies

Artuch, R.

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

Arzimanoglou, Alexis

SEEG in ... Family

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Barrea, Christophe

Lafora Disease and Diabetes: Enlarging Clinical Phenotype

Bastos, F.

A New Neurodegenerative Disease of Childhood

Battaglia, D.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Battini, R.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Bertini, E.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Bierau, J.

ITPA Encephalopathy: A Unique Neuroradiology Pattern as a Hallmark of the Disease

Blanchet, Catherine

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Bompard, S.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Boni, Antonella

Early Epilepsy Surgery in a Patient with Infantile Spasms and Focal Seizures, Due to Focal Cortical Dysplasia, and TSC2 Gene Mutation: Considerations about the Impact of Gene Mutation on the Correct Surgical Timing in the Presurgical Evaluation

Bousquet, I.

Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Bova, S.

Targeted Therapy in Channelopathies

Briola, F. La

Early Seizure Onset in TSC: Probing for Prognostic Markers

Brisca, Giacomo

Epilepsy and Other Clinical Features in a Child with Partial Deletion of Chromosome 15 Q

Brunetti, S.

Incontinentia Pigmenti in a Newborn Male with Klinefelter Syndrome: Clinical, Electroencephalographic, and Neuroimaging Findings

Caillaud, C.

Skin Biopsy in Ceroid Lipofuscinosis

Campistol, Jaume

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Canevini, M.P.

Early Seizure Onset in TSC: Probing for Prognostic Markers

Caporali, Camilla

CDKL5 Encephalopathy in Males: Follow-Up in Three Patients, New Insight in Phenotypical Spectrum, and Overview of Literature

Capra, Valeria

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Carme, Emilie

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Castellotti, B.

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Cereda, C.

Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Cereda, Cristina

CDKL5 Encephalopathy in Males: Follow-Up in Three Patients, New Insight in Phenotypical Spectrum, and Overview of Literature

Cervi, F.

Early Seizure Onset in TSC: Probing for Prognostic Markers

Ciano, C.

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Clapuyt, P.

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Epilepsy and Other Clinical Features in a Child with Partial Deletion of Chromosome 15 Q

Contaldo, I.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Cordani, R.

Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases

Cortès-Saladelafont, E.

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

Cossu, Massimo

Early Epilepsy Surgery in a Patient with Infantile Spasms and Focal Seizures, Due to Focal Cortical Dysplasia, and TSC2 Gene Mutation: Considerations about the Impact of Gene Mutation on the Correct Surgical Timing in the Presurgical Evaluation

Costanzo, C.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Croci, C.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases

De Bellescize, Julitta De Regnaud

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De Giorgis, V.

Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

De Giorgis, Valentina

CDKL5 Encephalopathy in Males: Follow-Up in Three Patients, New Insight in Phenotypical Spectrum, and Overview of Literature

De Grandis, E.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases

de Haller, Raoul

GLUT1-DS in a Girl with Transitory Abnormal Eye Movements and Seizures Responding to Carbamazepine

De Simone, M.

Incontinentia Pigmenti in a Newborn Male with Klinefelter Syndrome: Clinical, Electroencephalographic, and Neuroimaging Findings

Errichiello, E.

Targeted Therapy in Channelopathies

Fazzi, E.

Variable Phenotype Expression of a Maternally Inherited 16P13.11 Deletion in Twin Brothers with Epilepsy

Incontinentia Pigmenti in a Newborn Male with Klinefelter Syndrome: Clinical, Electroencephalographic, and Neuroimaging Findings

Developmental Delay, Tremors, and EEG Abnormalities: A Case of KCTD7 Gene Mutation

Filippo, Santorelli

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Fodstad, H.

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Fons, C.

ITPA Encephalopathy: A Unique Neuroradiology Pattern as a Hallmark of the Disease

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

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Fons, Carmen

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Metabolic Diseases with Epilepsy Vitamin Responsive Conditions

Freri, Elena

CDKL5 Encephalopathy in Males: Follow-Up in Three Patients, New Insight in Phenotypical Spectrum, and Overview of Literature

Galli, J.

Variable Phenotype Expression of a Maternally Inherited 16P13.11 Deletion in Twin Brothers with Epilepsy

Gambara, S.

Variable Phenotype Expression of a Maternally Inherited 16P13.11 Deletion in Twin Brothers with Epilepsy

Developmental Delay, Tremors, and EEG Abnormalities: A Case of KCTD7 Gene Mutation

Gambardella, M. L.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Garcia-Cazorla, A.

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

Grin1-Related Early Onset Encephalopathy: A Distinct NMDA Receptor Dysfunction

Gellera, C.

Targeted Therapy in Channelopathies

Gelot, A. Bernabe

Skin Biopsy in Ceroid Lipofuscinosis

Giacomini, T.

Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases

Giliani, S. C.

Incontinentia Pigmenti in a Newborn Male with Klinefelter Syndrome: Clinical, Electroencephalographic, and Neuroimaging Findings

Giuseppe, Gobbi

Ceroid Lipofuscinosis Type 2 (CLN-2): What Are the Early Neurophysiological Signs?

Gobbi, Giuseppe

Early Epilepsy Surgery in a Patient with Infantile Spasms and Focal Seizures, Due to Focal Cortical Dysplasia, and TSC2 Gene Mutation: Considerations about the Impact of Gene Mutation on the Correct Surgical Timing in the Presurgical Evaluation

Gobert, C.

Epilepsy with Myoclonic Absence in a Patient with COL4A1-Related Disorder: A Case Report

Gualdi, G.

Incontinentia Pigmenti in a Newborn Male with Klinefelter Syndrome: Clinical, Electroencephalographic, and Neuroimaging Findings

Hamel, Christian

Bulbar Palsy with Sensorial Impairment: An Amazing Outcome!!

Koch, E. Coelho De Oliviera

GLUT1-DS in a Girl with Transitory Abnormal Eye Movements and Seizures Responding to Carbamazepine

Korff, Christian

GLUT1-DS in a Girl with Transitory Abnormal Eye Movements and Seizures Responding to Carbamazepine

Lebon, S.

A New Neurodegenerative Disease of Childhood

Leroy, Patricia

Lafora Disease and Diabetes: Enlarging Clinical Phenotype

Lesca, G.

Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Lesca, Gaetan

The Contribution of Genetic Counseling to the Management of Childhood Epilepsies

SEEG in ... Family

Loreto, M.

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

Malerba, L.

Developmental Delay, Tremors, and EEG Abnormalities: A Case of KCTD7 Gene Mutation

Mancardi, M. M.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Mancardi, M.M.

Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases

Margherita, Santucci

Ceroid Lipofuscinosis Type 2 (CLN-2): What Are the Early Neurophysiological Signs?

Martelli, P.

Incontinentia Pigmenti in a Newborn Male with Klinefelter Syndrome: Clinical, Electroencephalographic, and Neuroimaging Findings

Masnada, S.

Targeted Therapy in Channelopathies

Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Masnada, Silvia

CDKL5 Encephalopathy in Males: Follow-Up in Three Patients, New Insight in Phenotypical Spectrum, and Overview of Literature

Melnikova, Anastasia Martinez-Esteve

Diagnostic Exome Sequencing in Patients with Epilepsy

Merlie, Alice Veauville

Bulbar Palsy with Sensorial Impairment: An Amazing Outcome!!

Messana, Tullio

Early Epilepsy Surgery in a Patient with Infantile Spasms and Focal Seizures, Due to Focal Cortical Dysplasia, and TSC2 Gene Mutation: Considerations about the Impact of Gene Mutation on the Correct Surgical Timing in the Presurgical Evaluation

Meunier, Isabelle

Bulbar Palsy with Sensorial Impairment: An Amazing Outcome!!

Meyer, Pierre

Bulbar Palsy with Sensorial Impairment: An Amazing Outcome!!

Minassian, Berge A.

Lafora Disease: A Perspective in Molecular Mechanism and Pathology

Mingarelli, A.

Early Seizure Onset in TSC: Probing for Prognostic Markers

Molina, C.

ITPA Encephalopathy: A Unique Neuroradiology Pattern as a Hallmark of the Disease

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

Molinaro, A.

Incontinentia Pigmenti in a Newborn Male with Klinefelter Syndrome: Clinical, Electroencephalographic, and Neuroimaging Findings

Moresco, Luca

Epilepsy and Other Clinical Features in a Child with Partial Deletion of Chromosome 15 Q

Musto, E.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Møller, Rikke Steensbjerre

Why You Need to Consider Genetic Testing of Children with Epilepsy

Nassogne, M. C.

Epilepsy with Myoclonic Absence in a Patient with COL4A1-Related Disorder: A Case Report

Nicolai, E.

Epilepsy with Myoclonic Absence in a Patient with COL4A1-Related Disorder: A Case Report

Nicolescu, Ramona

Lafora Disease and Diabetes: Enlarging Clinical Phenotype

O'Callaghan, M.

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

Olivella, M.

Grin1-Related Early Onset Encephalopathy: A Distinct NMDA Receptor Dysfunction

Olivieri, G.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Olivieri, I.

Targeted Therapy in Channelopathies

Orcesi, S.

Targeted Therapy in Channelopathies

Ormazabal, A.

ITPA Encephalopathy: A Unique Neuroradiology Pattern as a Hallmark of the Disease

Pagani, F.

Developmental Delay, Tremors, and EEG Abnormalities: A Case of KCTD7 Gene Mutation

Palau, Francesc

Diagnostic Exome Sequencing in Patients with Epilepsy

Panagiotakaki, Eleni

SEEG in ... Family

Papalia, G.

Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Papalia, Grazia

CDKL5 Encephalopathy in Males: Follow-Up in Three Patients, New Insight in Phenotypical Spectrum, and Overview of Literature

Pasca, L.

Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Pasca, Ludovica

CDKL5 Encephalopathy in Males: Follow-Up in Three Patients, New Insight in Phenotypical Spectrum, and Overview of Literature

Pavanello, M.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Peron, A.

Early Seizure Onset in TSC: Probing for Prognostic Markers

Perulli, M.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Pichiecchio, A.

Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Pinelli, L.

Incontinentia Pigmenti in a Newborn Male with Klinefelter Syndrome: Clinical, Electroencephalographic, and Neuroimaging Findings

Pini, Antonella

Early Epilepsy Surgery in a Patient with Infantile Spasms and Focal Seizures, Due to Focal Cortical Dysplasia, and TSC2 Gene Mutation: Considerations about the Impact of Gene Mutation on the Correct Surgical Timing in the Presurgical Evaluation

Pisciotta, L.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases

Prato, G.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases

Pulitanò, S.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Quinodoz, M.

A New Neurodegenerative Disease of Childhood

Quintiliani, M.

Epileptic Encephalopathy with Recurrent Focal Status Epilepticus and Epilepsia Partialis Continua in Patient with De Novo DNM1L Mutation: Electroclinical Features

Raffaella, Faggioli

Ceroid Lipofuscinosis Type 2 (CLN-2): What Are the Early Neurophysiological Signs?

Ramirez, A.

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

Ramirez-Camacho, Alia

Diagnostic Exome Sequencing in Patients with Epilepsy

Ranza, Emmanuelle

GLUT1-DS in a Girl with Transitory Abnormal Eye Movements and Seizures Responding to Carbamazepine

Righini, A.

Targeted Therapy in Channelopathies

Rivier, François

Bulbar Palsy with Sensorial Impairment: An Amazing Outcome!!

Rivolta, C.

A New Neurodegenerative Disease of Childhood

Roubertie, Agathe

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Roulet, E.

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Royer-Bertrand, B.

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Russo, Angelo

Early Epilepsy Surgery in a Patient with Infantile Spasms and Focal Seizures, Due to Focal Cortical Dysplasia, and TSC2 Gene Mutation: Considerations about the Impact of Gene Mutation on the Correct Surgical Timing in the Presurgical Evaluation

Sallemi, M.

Variable Phenotype Expression of a Maternally Inherited 16P13.11 Deletion in Twin Brothers with Epilepsy

Santucci, Margherita

Early Epilepsy Surgery in a Patient with Infantile Spasms and Focal Seizures, Due to Focal Cortical Dysplasia, and TSC2 Gene Mutation: Considerations about the Impact of Gene Mutation on the Correct Surgical Timing in the Presurgical Evaluation

Savini, M.

Early Seizure Onset in TSC: Probing for Prognostic Markers

Scmitt, A.

Skin Biopsy in Ceroid Lipofuscinosis

Severino, M.S.

Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases

Severino, S.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Sigatulina, M.

Neurotransmitter Depletion in Early Epileptic Encephalopathies and Possible Therapeutic Options

Siri, Laura

Epilepsy and Other Clinical Features in a Child with Partial Deletion of Chromosome 15 Q

Snazjer, Y.

Epilepsy with Myoclonic Absence in a Patient with COL4A1-Related Disorder: A Case Report

Striano, Pasquale

Epilepsy and Other Clinical Features in a Child with Partial Deletion of Chromosome 15 Q

Superti-Furga, A.

A New Neurodegenerative Disease of Childhood

Tassi, Laura

Early Epilepsy Surgery in a Patient with Infantile Spasms and Focal Seizures, Due to Focal Cortical Dysplasia, and TSC2 Gene Mutation: Considerations about the Impact of Gene Mutation on the Correct Surgical Timing in the Presurgical Evaluation

Teutonico, F.

Targeted Therapy in Channelopathies

Thevenon, Julien

SEEG in ... Family

Tonduti, D.

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Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Toni, Francesco

Early Epilepsy Surgery in a Patient with Infantile Spasms and Focal Seizures, Due to Focal Cortical Dysplasia, and TSC2 Gene Mutation: Considerations about the Impact of Gene Mutation on the Correct Surgical Timing in the Presurgical Evaluation

Tortora, D.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Tullio, Messana

Ceroid Lipofuscinosis Type 2 (CLN-2): What Are the Early Neurophysiological Signs?

Tzialla, C.

Targeted Therapy in Channelopathies

Uccella, S.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases

Valente, M.

Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Valente, Marialuisa

CDKL5 Encephalopathy in Males: Follow-Up in Three Patients, New Insight in Phenotypical Spectrum, and Overview of Literature

Varesio, C.

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Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Varesio, Costanza

CDKL5 Encephalopathy in Males: Follow-Up in Three Patients, New Insight in Phenotypical Spectrum, and Overview of Literature

Veggiotti, P.

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Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Veggiotti, Pierangelo

CDKL5 Encephalopathy in Males: Follow-Up in Three Patients, New Insight in Phenotypical Spectrum, and Overview of Literature

Glut 1 DS: Very Rare Disease or Underdiagnosed Syndrome?

Veneselli, E.

Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern

Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases

Verhalen, Brandy

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Vianey-Saban, Christine

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Vignoli, A.

Early Seizure Onset in TSC: Probing for Prognostic Markers

Ville, D.

Long-Term Follow-Up in Two Families with Adenylosuccinate Lyase Deficiency and Genotype: Phenotype Correlations through a Revision of Literature

Vrielynck, P.

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