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Federico Sicca

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Giulia Valvo; Orsetta Zuffardi; Paola Brovedani; Anna Rita Ferrari; Renzo Guerrini; Francesca Novara; Federico Sicca
22q11.2 Microduplication syndrome and epilepsy with continuous spikes and waves during sleep (CSWS). A case report and review of the literature.
Carla Marini; Massimo Mastrangelo; Davide Mei; Lucio Parmeggiani; Tiziana Pisano; Paolo Ricciardelli; Federico Sicca; Luigina Spaccini; Nicola Specchio; Alessandra Terracciano; Federico Vigevano; Nelia Zamponi; Patrizia Accorsi; Domenica Battaglia; Lorella Caffi; Maria Paola Canevini; Maria Lucia Canopoli; Elisabetta Cesaroni; Raffaella Cusmai; Bernardo Dalla Bernardina; Francesca Darra; Annarita Ferrari; Tiziana Granata; Salvatore Grosso; Renzo Guerrini
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy.
Nicola Specchio; Alessandra Terracciano; Marina Trivisano; Bernardo Dalla Bernardina; Enrico Bertini; Raffaella Cusmai; Francesca Darra; Lucia Fusco; Renzo Guerrini; Carla Marini; Davide Mei; Federico Sicca; Federico Vigevano
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.

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All Publications

2012: Giulia Valvo; Orsetta Zuffardi; Paola Brovedani; Anna Rita Ferrari; Renzo Guerrini; Francesca Novara; Federico Sicca
22q11.2 Microduplication syndrome and epilepsy with continuous spikes and waves during sleep (CSWS). A case report and review of the literature.
Epilepsy & behavior : E&B 2012;25(4):567-72.
2012: Carla Marini; Massimo Mastrangelo; Davide Mei; Lucio Parmeggiani; Tiziana Pisano; Paolo Ricciardelli; Federico Sicca; Luigina Spaccini; Nicola Specchio; Alessandra Terracciano; Federico Vigevano; Nelia Zamponi; Patrizia Accorsi; Domenica Battaglia; Lorella Caffi; Maria Paola Canevini; Maria Lucia Canopoli; Elisabetta Cesaroni; Raffaella Cusmai; Bernardo Dalla Bernardina; Francesca Darra; Annarita Ferrari; Tiziana Granata; Salvatore Grosso; Renzo Guerrini
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy.
Epilepsia 2012;53(12):2111-9.
2011: Nicola Specchio; Alessandra Terracciano; Marina Trivisano; Bernardo Dalla Bernardina; Enrico Bertini; Raffaella Cusmai; Francesca Darra; Lucia Fusco; Renzo Guerrini; Carla Marini; Davide Mei; Federico Sicca; Federico Vigevano
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.
Epilepsia 2011;52(7):1251-7.
2011: Federico Sicca; Paola Imbrici; Maria Cristina D'Adamo; Francesca Moro; Fabrizia Bonatti; Paola Brovedani; Alessandro Grottesi; Renzo Guerrini; Gabriele Masi; Filippo Maria Santorelli; Mauro Pessia
Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.
Neurobiology of disease 2011;43(1):239-47.
2011: Pasquale Striano; Roberta Paravidino; Federico Sicca; P Chiurazzi; stefania gimelli; Antonino Coppola; A Robbiano; Monica Traverso; M Pintaudi; S Giovannini; F Operto; P Vigliano; Tiziana Granata; Giangennaro Coppola; Antonino Romeo; Nicola Specchio; Lucio Giordano; Lucy Osborne; G Gimelli; Carlo Minetti; Federico Zara
West syndrome associated with 14q12 duplications harboring FOXG1.
Neurology 2011;76(18):1600-2.
2007: Carla Marini; Davide Mei; Teresa Temudo; Anna Rita Ferrari; Daniela Buti; Charlotte Dravet; Ana I Dias; Ana Moreira; Eulalia Calado; Stefano Seri; Brian Neville; Juan Narbona; Evan Reid; Roberto Michelucci; Federico Sicca; Helen J Cross; Renzo Guerrini
Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.
Epilepsia 2007;48(9):1678-85.
2006: Antonella Gritti; Federico Sicca; Antonella Di Sarno; Nicolina Di Cosmo; Serena Vajro; Pietro Vajro
Emotional and behavioral problems after pediatric liver transplantation: a quantitative assessment.
Pediatric transplantation 2006;10(2):205-9.
2004: Renzo Guerrini; Davide Mei; S Sisodiya; Federico Sicca; B Harding; Yukitoshi Takahashi; Thomas Dorn; A Yoshida; J Campistol; G Krämer; Francesca Moro; William B Dobyns; Elena Parrini
Germline and mosaic mutations of FLN1 in men with periventricular heterotopia.
Neurology 2004;63(1):51-6.
2003: Federico Sicca; A Kelemen; Pierre Genton; S Das; Davide Mei; Francesca Moro; William B Dobyns; Renzo Guerrini
Mosaic mutations of the LIS1 gene cause subcortical band heterotopia.
Neurology 2003;61(8):1042-6.
2003: Renzo Guerrini; Federico Sicca; Lucio Parmeggiani
Epilepsy and malformations of the cerebral cortex.
Epileptic disorders : international epilepsy journal with videotape 2003;5 Suppl 2():S9-26.
2003: Federico Sicca; Margherita Silengo; Elena Parrini; Giovanni Battista Ferrero; Renzo Guerrini
Subcortical band heterotopia with simplified gyral pattern and syndactyly.
American journal of medical genetics. Part A 2003;119A(2):207-10.
2000: Federico Sicca; A Contaldo; E Rey; Olivier Dulac
Phenytoin administration in the newborn and infant.
Brain & development 2000;22(1):35-40.