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Renzo Guerrini

Showing results (471-480 of 611) with videos related to

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Neurology|May 11, 2016
Definition and diagnostic criteria of sleep-related hypermotor epilepsyPaolo Tinuper, Francesca Bisulli, J H Cross, et al.
Journal of Neuropathology and Experimental Neurology|December 4, 2020
Somatic Focal Copy Number Gains of Noncoding Regions of Receptor Tyrosine Kinase Genes in Treatment-Resistant EpilepsyVarshini Vasudevaraja, Javier Hernaez Rodriguez, Cristiana Pelorosso, et al.
The Journal of Allergy and Clinical Immunology|April 29, 2014
Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spotsGiancarlo la Marca, Clementina Canessa, Elisa Giocaliere, et al.
Neurology|September 2, 2018
The phenotype of <i>SCN8A</i> developmental and epileptic encephalopathyElena Gardella, Carla Marini, Marina Trivisano, et al.
Human Genetics|July 3, 2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2Lyndal Henden, Saskia Freytag, Zaid Afawi, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2016
Idiopathic focal epilepsies: the "lost tribe"Deb K Pal, Colin Ferrie, Laura Addis, et al.
Epilepsia|October 25, 2025
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiologySimona Balestrini, Ilaria Galli, Maria Luisa Ricci, et al.
Epilepsia|June 16, 2022
The ILAE consensus classification of focal cortical dysplasia: An update proposed by an ad hoc task force of the ILAE diagnostic methods commissionImad Najm, Dennis Lal, Mario Alonso Vanegas, et al.
Brain : a Journal of Neurology|November 6, 2019
Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive courseAlessandro Esposito, Antonio Falace, Matias Wagner, et al.
Epilepsia|April 30, 2009
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosisCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
Pageof 62

Showing results (471-480 of 611) with videos related to

Sort By:
Pageof 62
Neurology|May 11, 2016
Definition and diagnostic criteria of sleep-related hypermotor epilepsyPaolo Tinuper, Francesca Bisulli, J H Cross, et al.
Journal of Neuropathology and Experimental Neurology|December 4, 2020
Somatic Focal Copy Number Gains of Noncoding Regions of Receptor Tyrosine Kinase Genes in Treatment-Resistant EpilepsyVarshini Vasudevaraja, Javier Hernaez Rodriguez, Cristiana Pelorosso, et al.
The Journal of Allergy and Clinical Immunology|April 29, 2014
Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spotsGiancarlo la Marca, Clementina Canessa, Elisa Giocaliere, et al.
Neurology|September 2, 2018
The phenotype of <i>SCN8A</i> developmental and epileptic encephalopathyElena Gardella, Carla Marini, Marina Trivisano, et al.
Human Genetics|July 3, 2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2Lyndal Henden, Saskia Freytag, Zaid Afawi, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2016
Idiopathic focal epilepsies: the "lost tribe"Deb K Pal, Colin Ferrie, Laura Addis, et al.
Epilepsia|October 25, 2025
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiologySimona Balestrini, Ilaria Galli, Maria Luisa Ricci, et al.
Epilepsia|June 16, 2022
The ILAE consensus classification of focal cortical dysplasia: An update proposed by an ad hoc task force of the ILAE diagnostic methods commissionImad Najm, Dennis Lal, Mario Alonso Vanegas, et al.
Brain : a Journal of Neurology|November 6, 2019
Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive courseAlessandro Esposito, Antonio Falace, Matias Wagner, et al.
Epilepsia|April 30, 2009
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosisCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
Pageof 62