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Renzo Guerrini

Showing results (191-200 of 610) with videos related to

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Epilepsia|April 6, 2011
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: an Italian consensusPierangelo Veggiotti, Alberto Burlina, Giangennaro Coppola, et al.
Epilepsia|October 24, 2006
Autosomal dominant early-onset cortical myoclonus, photic-induced myoclonus, and epilepsy in a large pedigreeElena Gardella, Paolo Tinuper, Carla Marini, et al.
American Journal of Medical Genetics. Part A|August 26, 2018
Familial dominant epilepsy and mild pachygyria associated with a constitutional LIS1 mutationDalila De Vita, Davide Mei, Domenico Rutigliano, et al.
American Journal of Medical Genetics. Part A|May 19, 2021
Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 geneSara Brunetti, Laura Malerba, Lucio Giordano, et al.
Biomedicines|August 26, 2022
Fluorescent In Situ Staining and Flow Cytometric Procedures as New Pre-Diagnostic Tests for Sialidosis, GM1 Gangliosidosis and Niemann-Pick Type CClaudia Capitini, Federica Feo, Anna Caciotti, et al.
Epilepsia|April 18, 2018
Long-term efficacy of add-on lacosamide treatment in children and adolescents with refractory epilepsies: A single-center observational studyAnna Rosati, Lucrezia Ilvento, Riccardo Rizzi, et al.
Molecular Genetics and Metabolism Reports|August 31, 2019
Broadening phenotype of adenylosuccinate lyase deficiency: A novel clinical pattern resembling neuronal ceroid lipofuscinosisMario Mastrangelo, Chiara Alfonsi, Isabella Screpanti, et al.
Epilepsia|January 22, 2005
Abnormal phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutationTiziana Pisano, Carla Marini, Paola Brovedani, et al.
Epilepsia|April 20, 2007
Proposal of an algorithm for diagnosis and treatment of neonatal seizures in developing countriesJohn Patrick T Co, Maurizio Elia, Jerome Engel, et al.
European Journal of Human Genetics : EJHG|November 1, 2006
Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locusClaudia Torniero, Bernardo dalla Bernardina, Francesca Novara, et al.
Pageof 61

Showing results (191-200 of 610) with videos related to

Sort By:
Pageof 61
Epilepsia|April 6, 2011
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: an Italian consensusPierangelo Veggiotti, Alberto Burlina, Giangennaro Coppola, et al.
Epilepsia|October 24, 2006
Autosomal dominant early-onset cortical myoclonus, photic-induced myoclonus, and epilepsy in a large pedigreeElena Gardella, Paolo Tinuper, Carla Marini, et al.
American Journal of Medical Genetics. Part A|August 26, 2018
Familial dominant epilepsy and mild pachygyria associated with a constitutional LIS1 mutationDalila De Vita, Davide Mei, Domenico Rutigliano, et al.
American Journal of Medical Genetics. Part A|May 19, 2021
Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 geneSara Brunetti, Laura Malerba, Lucio Giordano, et al.
Biomedicines|August 26, 2022
Fluorescent In Situ Staining and Flow Cytometric Procedures as New Pre-Diagnostic Tests for Sialidosis, GM1 Gangliosidosis and Niemann-Pick Type CClaudia Capitini, Federica Feo, Anna Caciotti, et al.
Epilepsia|April 18, 2018
Long-term efficacy of add-on lacosamide treatment in children and adolescents with refractory epilepsies: A single-center observational studyAnna Rosati, Lucrezia Ilvento, Riccardo Rizzi, et al.
Molecular Genetics and Metabolism Reports|August 31, 2019
Broadening phenotype of adenylosuccinate lyase deficiency: A novel clinical pattern resembling neuronal ceroid lipofuscinosisMario Mastrangelo, Chiara Alfonsi, Isabella Screpanti, et al.
Epilepsia|January 22, 2005
Abnormal phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutationTiziana Pisano, Carla Marini, Paola Brovedani, et al.
Epilepsia|April 20, 2007
Proposal of an algorithm for diagnosis and treatment of neonatal seizures in developing countriesJohn Patrick T Co, Maurizio Elia, Jerome Engel, et al.
European Journal of Human Genetics : EJHG|November 1, 2006
Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locusClaudia Torniero, Bernardo dalla Bernardina, Francesca Novara, et al.
Pageof 61