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Beatriz G Giraldez

Showing results (1-10 of 7) with videos related to

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Epilepsia|March 30, 2023
Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbiditiesBeatriz G Giraldez, José M Serratosa, Salvatore Striano, et al.
Seizure|May 21, 2019
External trigeminal nerve stimulation: A long term follow up studyLaura Olivié, Beatriz G Giraldez, Alba Sierra-Marcos, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 21, 2020
Expanding the clinical and EEG spectrum of CNKSR2-related encephalopathy with status epilepticus during slow sleep (ESES)Claudia M Bonardi, Cyril Mignot, Jose M Serratosa, et al.
American Journal of Human Genetics|November 12, 2013
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndromeArvid Suls, Johanna A Jaehn, Angela Kecskés, et al.
Brain : a Journal of Neurology|October 21, 2017
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathiesSilvia Masnada, Ulrike B S Hedrich, Elena Gardella, et al.
Molecular Genetics & Genomic Medicine|July 29, 2016
Pitfalls in genetic testing: the story of missed SCN1A mutationsTania Djémié, Sarah Weckhuysen, Sarah von Spiczak, et al.
Neurology|June 26, 2025
Phenotypic Spectrum in Individuals With Pathogenic <i>GABRG2</i> Loss- and Gain-of-Function VariantsAlessandra Rossi, Susan X N Lin, Nathan L Absalom, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Epilepsia|March 30, 2023
Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbiditiesBeatriz G Giraldez, José M Serratosa, Salvatore Striano, et al.
Seizure|May 21, 2019
External trigeminal nerve stimulation: A long term follow up studyLaura Olivié, Beatriz G Giraldez, Alba Sierra-Marcos, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 21, 2020
Expanding the clinical and EEG spectrum of CNKSR2-related encephalopathy with status epilepticus during slow sleep (ESES)Claudia M Bonardi, Cyril Mignot, Jose M Serratosa, et al.
American Journal of Human Genetics|November 12, 2013
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndromeArvid Suls, Johanna A Jaehn, Angela Kecskés, et al.
Brain : a Journal of Neurology|October 21, 2017
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathiesSilvia Masnada, Ulrike B S Hedrich, Elena Gardella, et al.
Molecular Genetics & Genomic Medicine|July 29, 2016
Pitfalls in genetic testing: the story of missed SCN1A mutationsTania Djémié, Sarah Weckhuysen, Sarah von Spiczak, et al.
Neurology|June 26, 2025
Phenotypic Spectrum in Individuals With Pathogenic <i>GABRG2</i> Loss- and Gain-of-Function VariantsAlessandra Rossi, Susan X N Lin, Nathan L Absalom, et al.
Pageof 1