Roberta Paravidino - Concepedia

Author

Roberta Paravidino

Istituto Giannina Gaslini

Also Known As

R. Paravidino, Roberta Paravidino

Publications

838

Citations

H-Index

Concepts

All Affiliations

Istituto Giannina Gaslini Ente Ospedaliero Ospedali Galliera Bambino Gesù Children's Hospital Azienda Ospedaliera Carlo Poma Ospedale San Donato

About

Roberta Paravidino is an author at Istituto Giannina Gaslini specializing in neurology, medicine, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	109
2	Public Health	1	1	55
3	Social Sciences	1	1	54
4	Molecular Genetics	1	1	55
5	Molecular Medicine	1	1	55

Roberta Paravidino

Publications

641

Citations

H-Index

Page 1

	Year	Citations
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance Federico Zara, Nicola Specchio, Pasquale Striano, Epilepsia	2013	122
PRRT2 Mutations are the major cause of benign familial infantile seizures Julian Schubert, Roberta Paravidino, Felicitas Becker, Human Mutation	2012	104
Brain MRI Findings in Severe Myoclonic Epilepsy in Infancy and Genotype–Phenotype Correlations Pasquale Striano, Maria Margherita Mancardi, Roberta Biancheri, Epilepsia	2007	92
Cryptic chromosome deletions involving <i>SCN1A</i> in severe myoclonic epilepsy of infancy Francesca Madia, Pasquale Striano, Elena Di Gennaro, Neurology	2006	79
Loss‐of‐function <i><scp>KCNH</scp>2</i> mutation in a family with long <scp>QT</scp> syndrome, epilepsy, and sudden death Sara Partemi, Sandrine Cestèle, Marianna Pezzella, Epilepsia	2013	67
West syndrome associated with 14q12 duplications harboring FOXG1 Pasquale Striano, Roberta Paravidino, Federico Sicca, Neurology Brain DevelopmentGeneticsWest SyndromeGenetic EpidemiologyDiagnosis	2011	55
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy Ida Manna, Antonio Gambardella, Amedeo Bianchi, Epilepsia Scn1a PolymorphismGenetic EpidemiologyHuman PolymorphismPharmacotherapySocial Sciences	2011	54
Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with<i>SCN1A</i>Mutations Maria Margherita Mancardi, Pasquale Striano, Elena Di Gennaro, Epilepsia	2006	54
A very fast and accurate method for calling aberrations in array-CGH data Matteo Benelli, Giuseppina Marseglia, Genni Nannetti, Biostatistics	2010	14

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