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Carla Marini

Showing results (41-50 of 161) with videos related to

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Developmental Medicine and Child Neurology|February 12, 2011
CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of lifeFederico Melani, Davide Mei, Tiziana Pisano, et al.
Veterinary Journal (London, England : 1997)|March 25, 2014
Evaluation of storage conditions on equine adipose tissue-derived multipotent mesenchymal stromal cellsFrancesca Mercati, Luisa Pascucci, Giovanni Curina, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 7, 2007
Intracortical hyperexcitability in humans with a GABAA receptor mutationMarco Fedi, Samuel F Berkovic, Richard A L Macdonell, et al.
Neuroscience Letters|July 20, 2005
No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizuresFilippo Martinelli Boneschi, Paolo Aridon, Federico Zara, et al.
American Journal of Medical Genetics. Part A|May 2, 2013
Clinical and genetic study of a family with a paternally inherited 15q11-q13 duplicationCarla Marini, Antonella Cecconi, Elisa Contini, et al.
Neurology|October 19, 2012
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraineCarla Marini, Valerio Conti, Davide Mei, 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|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.
Archives of Neurology|May 10, 2006
Distinguishing sleep disorders from seizures: diagnosing bumps in the nightChristopher Paul Derry, Margot Davey, Murray Johns, et al.
Epilepsia|October 1, 2014
Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boysDavide Mei, Francesca Darra, Carmen Barba, et al.
Pageof 17

Showing results (41-50 of 161) with videos related to

Sort By:
Pageof 17
Developmental Medicine and Child Neurology|February 12, 2011
CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of lifeFederico Melani, Davide Mei, Tiziana Pisano, et al.
Veterinary Journal (London, England : 1997)|March 25, 2014
Evaluation of storage conditions on equine adipose tissue-derived multipotent mesenchymal stromal cellsFrancesca Mercati, Luisa Pascucci, Giovanni Curina, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 7, 2007
Intracortical hyperexcitability in humans with a GABAA receptor mutationMarco Fedi, Samuel F Berkovic, Richard A L Macdonell, et al.
Neuroscience Letters|July 20, 2005
No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizuresFilippo Martinelli Boneschi, Paolo Aridon, Federico Zara, et al.
American Journal of Medical Genetics. Part A|May 2, 2013
Clinical and genetic study of a family with a paternally inherited 15q11-q13 duplicationCarla Marini, Antonella Cecconi, Elisa Contini, et al.
Neurology|October 19, 2012
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraineCarla Marini, Valerio Conti, Davide Mei, 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|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.
Archives of Neurology|May 10, 2006
Distinguishing sleep disorders from seizures: diagnosing bumps in the nightChristopher Paul Derry, Margot Davey, Murray Johns, et al.
Epilepsia|October 1, 2014
Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boysDavide Mei, Francesca Darra, Carmen Barba, et al.
Pageof 17