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Carla Marini

Showing results (61-70 of 161) with videos related to

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Neurology|March 15, 2015
Nocturnal frontal lobe epilepsy with paroxysmal arousals due to CHRNA2 loss of functionValerio Conti, Patrizia Aracri, Laura Chiti, et al.
Epilepsia|April 13, 2011
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutationsNicola Specchio, Carla Marini, Alessandra Terracciano, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defectsCarla Marini, Katia Hardies, Tiziana Pisano, et al.
Seizure|August 18, 2022
An Italian consensus on the management of Lennox-Gastaut syndromeAntonella Riva, Antonietta Coppola, Carlo Di Bonaventura, et al.
Translational Psychiatry|May 6, 2020
A standardized patient-centered characterization of the phenotypic spectrum of PCDH19 girls clustering epilepsyKristy L Kolc, Lynette G Sadleir, Christel Depienne, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 26, 2020
Quantitative MRI-Based Analysis Identifies Developmental Limbic Abnormalities in PCDH19 EncephalopathyMatteo Lenge, Carla Marini, Edoardo Canale, et al.
Epilepsia|January 24, 2004
Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutationsPaolo Bonanni, Michela Malcarne, Francesca Moro, et al.
Epilepsy Research|November 28, 2012
Do mutations in SCN1B cause Dravet syndrome?Young Ok Kim, Leanne Dibbens, Carla Marini, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|April 13, 2019
SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plusFrancesca Bisulli, Laura Licchetta, Sara Baldassari, et al.
Archives of Neurology|May 11, 2011
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsySaul A Mullen, Carla Marini, Arvid Suls, et al.
Pageof 17

Showing results (61-70 of 161) with videos related to

Sort By:
Pageof 17
Neurology|March 15, 2015
Nocturnal frontal lobe epilepsy with paroxysmal arousals due to CHRNA2 loss of functionValerio Conti, Patrizia Aracri, Laura Chiti, et al.
Epilepsia|April 13, 2011
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutationsNicola Specchio, Carla Marini, Alessandra Terracciano, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defectsCarla Marini, Katia Hardies, Tiziana Pisano, et al.
Seizure|August 18, 2022
An Italian consensus on the management of Lennox-Gastaut syndromeAntonella Riva, Antonietta Coppola, Carlo Di Bonaventura, et al.
Translational Psychiatry|May 6, 2020
A standardized patient-centered characterization of the phenotypic spectrum of PCDH19 girls clustering epilepsyKristy L Kolc, Lynette G Sadleir, Christel Depienne, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 26, 2020
Quantitative MRI-Based Analysis Identifies Developmental Limbic Abnormalities in PCDH19 EncephalopathyMatteo Lenge, Carla Marini, Edoardo Canale, et al.
Epilepsia|January 24, 2004
Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutationsPaolo Bonanni, Michela Malcarne, Francesca Moro, et al.
Epilepsy Research|November 28, 2012
Do mutations in SCN1B cause Dravet syndrome?Young Ok Kim, Leanne Dibbens, Carla Marini, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|April 13, 2019
SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plusFrancesca Bisulli, Laura Licchetta, Sara Baldassari, et al.
Archives of Neurology|May 11, 2011
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsySaul A Mullen, Carla Marini, Arvid Suls, et al.
Pageof 17