Publications by authors named "Roberto Gaggero"

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Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome.
Giovanna Lenci, Maria Grazia Calevo, Roberto Gaggero, Giulia Prato, Livia Pisciotta

Brain Dev· June 2019

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Early classification of childhood focal idiopathic epilepsies: is it possible at the first seizure?
Roberto Gaggero, Angela Pistorio, Sara Pignatelli, Alessandra Rossi, Maria Margherita Mancardi

Eur J Paediatr Neurol· May 2014

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Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
Federico Zara, Nicola Specchio, Pasquale Striano, Angela Robbiano, Elena Gennaro, Roberto Gaggero

Epilepsia· March 2013

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Epilepsy associated with supratentorial brain tumors under 3 years of life.
Roberto Gaggero, Alessandro Consales, Francesca Fazzini, Maria Margherita Mancardi, Maria Giuseppina Baglietto

Epilepsy Res· December 2009

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Clinical and electroencephalographic features in patients with CDKL5 mutations: two new Italian cases and review of the literature.
Maria Pintaudi, Maria Giuseppina Baglietto, Roberto Gaggero, Elena Parodi, Alice Pessagno

Epilepsy Behav· February 2008

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Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.
Pasquale Striano, Maria Margherita Mancardi, Roberta Biancheri, Francesca Madia, Elena Gennaro, Roberto Gaggero

Epilepsia· June 2007

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Severe epilepsy in X-linked creatine transporter defect (CRTR-D).
Maria Margherita Mancardi, Ubaldo Caruso, Maria Cristina Schiaffino, Maria Giuseppina Baglietto, Andrea Rossi, Roberto Gaggero

Epilepsia· June 2007

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Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations.
Pasquale Striano, Nicola Specchio, Roberta Biancheri, Natalia Cannelli, Alessandro Simonati, Roberto Gaggero

Epilepsy Behav· February 2007

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Intractable epilepsy secondary to cyclosporine toxicity in children undergoing allogeneic hematopoietic bone marrow transplantation.
Roberto Gaggero, Riccardo Haupt, Maria Paola Fondelli, Raffaella De Vescovi, Alessia Marino

J Child Neurol· October 2006

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Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations.
Maria Margherita Mancardi, Pasquale Striano, Elena Gennaro, Francesca Madia, Roberta Paravidino, Roberto Gaggero

Epilepsia· October 2006

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Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases.
Pasquale Striano, Michela Malacarne, Simona Cavani, Mauro Pierluigi, Rosanna Rinaldi, Roberto Gaggero

Am J Med Genet A· September 2006

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Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.
Pasquale Striano, Maria Luisa Lispi, Elena Gennaro, Francesca Madia, Monica Traverso, Roberto Gaggero

Epilepsia· June 2006

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Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the Mediterranean.
Natalia Cannelli, Denise Cassandrini, Enrico Bertini, Pasquale Striano, Lucia Fusco, Roberto Gaggero

Neurogenetics· May 2006

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6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
Maurizio Elia, Pasquale Striano, Marco Fichera, Roberto Gaggero, Lucia Castiglia

Epilepsia· May 2006

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Somatic and germline mosaicisms in severe myoclonic epilepsy of infancy.
Elena Gennaro, Filippo M Santorelli, Enrico Bertini, Daniela Buti, Roberto Gaggero

Biochem Biophys Res Commun· March 2006

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No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy.
Francesca Madia, Elena Gennaro, Massimiliano Cecconi, Daniela Buti, Giuseppe Capovilla, Roberto Gaggero

Epilepsy Res· March 2003

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Lack of SCN1A mutations in familial febrile seizures.
Michela Malacarne, Francesca Madia, Elena Gennaro, Daniela Vacca, A Ilter Güney, Roberto Gaggero

Epilepsia· May 2002

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