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Romina Combi

Showing results (11-20 of 36) with videos related to

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Journal of Personalized Medicine|January 21, 2022
Can SARS-CoV-2 Infection Exacerbate Alzheimer's Disease? An Overview of Shared Risk Factors and Pathogenetic MechanismsChiara Villa, Eleonora Rivellini, Marialuisa Lavitrano, et al.
Pharmaceutics|March 6, 2021
Patient-Derived Induced Pluripotent Stem Cells (iPSCs) and Cerebral Organoids for Drug Screening and Development in Autism Spectrum Disorder: Opportunities and ChallengesChiara Villa, Romina Combi, Donatella Conconi, et al.
Mechanisms of Ageing and Development|December 22, 2019
Potassium channels in the neuronal homeostasis and neurodegenerative pathways underlying Alzheimer's disease: An updateChiara Villa, Huriye Suphesiz, Romina Combi, et al.
International Journal of Molecular Sciences|April 30, 2021
Genetic Architecture and Molecular, Imaging and Prodromic Markers in Dementia with Lewy Bodies: State of the Art, Opportunities and ChallengesRomina Combi, Maria Salsone, Chiara Villa, et al.
Journal of Neurology|August 19, 2004
Autosomal dominant nocturnal frontal lobe epilepsy--a critical overviewRomina Combi, Leda Dalprà, Maria Luisa Tenchini, et al.
Annals of Neurology|October 14, 2005
Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone geneRomina Combi, Leda Dalprà, Luigi Ferini-Strambi, et al.
Journal of Sleep Research|November 29, 2011
A de novo mutation in an Italian sporadic patient affected by nocturnal frontal lobe epilepsyVeronica Sansoni, Lino Nobili, Paola Proserpio, et al.
Archives of Dermatological Research|March 4, 2019
Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencingFrancesca Cortini, Chiara Villa, Barbara Marinelli, et al.
Human Mutation|April 30, 2009
A rescuable folding defective Nav1.1 (SCN1A) sodium channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies?Raffaella Rusconi, Romina Combi, Sandrine Cestèle, et al.
Brain Research Bulletin|July 13, 2004
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsyRomina Combi, Leda Dalprà, Massimo Malcovati, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Journal of Personalized Medicine|January 21, 2022
Can SARS-CoV-2 Infection Exacerbate Alzheimer's Disease? An Overview of Shared Risk Factors and Pathogenetic MechanismsChiara Villa, Eleonora Rivellini, Marialuisa Lavitrano, et al.
Pharmaceutics|March 6, 2021
Patient-Derived Induced Pluripotent Stem Cells (iPSCs) and Cerebral Organoids for Drug Screening and Development in Autism Spectrum Disorder: Opportunities and ChallengesChiara Villa, Romina Combi, Donatella Conconi, et al.
Mechanisms of Ageing and Development|December 22, 2019
Potassium channels in the neuronal homeostasis and neurodegenerative pathways underlying Alzheimer's disease: An updateChiara Villa, Huriye Suphesiz, Romina Combi, et al.
International Journal of Molecular Sciences|April 30, 2021
Genetic Architecture and Molecular, Imaging and Prodromic Markers in Dementia with Lewy Bodies: State of the Art, Opportunities and ChallengesRomina Combi, Maria Salsone, Chiara Villa, et al.
Journal of Neurology|August 19, 2004
Autosomal dominant nocturnal frontal lobe epilepsy--a critical overviewRomina Combi, Leda Dalprà, Maria Luisa Tenchini, et al.
Annals of Neurology|October 14, 2005
Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone geneRomina Combi, Leda Dalprà, Luigi Ferini-Strambi, et al.
Journal of Sleep Research|November 29, 2011
A de novo mutation in an Italian sporadic patient affected by nocturnal frontal lobe epilepsyVeronica Sansoni, Lino Nobili, Paola Proserpio, et al.
Archives of Dermatological Research|March 4, 2019
Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencingFrancesca Cortini, Chiara Villa, Barbara Marinelli, et al.
Human Mutation|April 30, 2009
A rescuable folding defective Nav1.1 (SCN1A) sodium channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies?Raffaella Rusconi, Romina Combi, Sandrine Cestèle, et al.
Brain Research Bulletin|July 13, 2004
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsyRomina Combi, Leda Dalprà, Massimo Malcovati, et al.
Pageof 4