Silvana Franceschetti mostly deals with Epilepsy, Genetics, Neuroscience, Mutation and Pathology. Her studies deal with areas such as Neuropsychology, Pediatrics, Audiology and Electroencephalography as well as Epilepsy. Her work carried out in the field of Pediatrics brings together such families of science as Young adult, Disease, Etiology and Myoclonus.
Silvana Franceschetti interconnects Artificial neural network, Central nervous system disease, Support vector machine and Feature vector in the investigation of issues within Electroencephalography. The Neuroscience study which covers Glutamate receptor that intersects with Acetylcholine, Periventricular Region and gamma-Aminobutyric acid. Her Pathology research is multidisciplinary, relying on both Ether-A-Go-Go Potassium Channels, Cell culture and Psychomotor delay.
Silvana Franceschetti focuses on Epilepsy, Neuroscience, Electroencephalography, Myoclonus and Progressive myoclonus epilepsy. Silvana Franceschetti has researched Epilepsy in several fields, including Internal medicine, Pediatrics and Pathology. Her Electroencephalography study combines topics from a wide range of disciplines, such as Electromyography, Magnetic resonance imaging, Central nervous system disease and Audiology.
Her research investigates the connection with Audiology and areas like Neuropsychology which intersect with concerns in Developmental psychology. Her Myoclonus research integrates issues from Motor cortex, Somatosensory evoked potential and Neurological disorder. Her studies in Progressive myoclonus epilepsy integrate themes in fields like Kufs disease and Ataxia.
Her primary areas of study are Epilepsy, Electroencephalography, Genetics, Missense mutation and Audiology. Her research in Epilepsy intersects with topics in Disease, Pediatrics and Myoclonus. Her Electroencephalography research is multidisciplinary, incorporating elements of Anesthesia and Magnetic resonance imaging.
Her Missense mutation study also includes fields such as
Silvana Franceschetti mainly focuses on Epilepsy, Missense mutation, Genetics, Progressive myoclonus epilepsy and Mutation. Her Epilepsy study combines topics in areas such as Exome sequencing, Bioinformatics, Disease, Pediatrics and Genetic testing. Her work deals with themes such as Neocortex, Electrophysiology, Compound heterozygosity and Point mutation, which intersect with Missense mutation.
While the research belongs to areas of Progressive myoclonus epilepsy, she spends her time largely on the problem of Kufs disease, intersecting her research to questions surrounding Ataxia and Age of onset. Her work carried out in the field of Mutation brings together such families of science as Phenotype, Loss function and Gene isoform. Her research integrates issues of Neuroscience and Myoclonic epilepsy in her study of Etiology.
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Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage
Katherine R. Smith;Katherine R. Smith;John Damiano;Silvana Franceschetti;Stirling Carpenter.
American Journal of Human Genetics (2012)
Seizure control and treatment in pregnancy: Observations from the EURAP epilepsy pregnancy registry
Torbjörn Tomson;D. Battino;E. Bonizzoni;J. Craig.
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Mikko Muona;Samuel F. Berkovic;Leanne M. Dibbens;Karen L. Oliver.
Nature Genetics (2015)
Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1
Kimmo Virtaneva;Elena D'Amato;Jinmin Miao;Marjaleena Koskiniemi.
Nature Genetics (1997)
Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures
Massimo Mantegazza;Antonio Gambardella;Raffaella Rusconi;Emanuele Schiavon.
Proceedings of the National Academy of Sciences of the United States of America (2005)
Epileptic phenotypes associated with mitochondrial disorders
L. Canafoglia;Silvana Franceschetti;C. Antozzi;F. Carrara.
Epileptogenic networks of type II focal cortical dysplasia: A stereo-EEG study
Giulia Varotto;Laura Tassi;Silvana Franceschetti;Roberto Spreafico.
hERG1 channels are overexpressed in glioblastoma multiforme and modulate VEGF secretion in glioblastoma cell lines
A Masi;A Becchetti;R Restano-Cassulini;S Polvani.
British Journal of Cancer (2005)
Kufs Disease, the Major Adult Form of Neuronal Ceroid Lipofuscinosis, Caused by Mutations in CLN6
Todor Arsov;Katherine R Smith;John Anthony Damiano;Silvana Franceschetti.
American Journal of Human Genetics (2011)
Intellectual and language findings and their relationship to EEG characteristics in benign childhood epilepsy with centrotemporal spikes.
Daria Riva;Chiara Vago;Silvana Franceschetti;Chiara Pantaleoni.
Epilepsy & Behavior (2007)
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