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G Claeys

Showing results (151-160 of 239) with videos related to

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Seizure|April 4, 2007
Epilepsy and migraine in a patient with Urbach-Wiethe diseaseKristl G Claeys, Lieve R F Claes, Johan W M Van Goethem, et al.
Neurology|April 27, 2007
Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9qL Deprez, K Peeters, W Van Paesschen, et al.
European Journal of Neurology|November 17, 2025
Novel Mutations in Titin Exon 363 With Different Phenotypes Including a Founder Mutation in Eastern EuropeVeronica Sian, Maria Francesca Di Feo, Sergei Kurbatov, et al.
Epilepsia|November 22, 2007
Epilepsy as part of the phenotype associated with ATP1A2 mutationsLiesbet Deprez, Sarah Weckhuysen, Katelijne Peeters, et al.
Human Mutation|December 21, 2020
Expanding the clinical and genetic spectrum of FDXR deficiency by functional validation of variants of uncertain significanceSarah L Stenton, Dorota Piekutowska-Abramczuk, Lea Kulterer, et al.
Acta Neuropathologica|December 17, 2008
"Necklace" fibers, a new histological marker of late-onset MTM1-related centronuclear myopathyJorge A Bevilacqua, Marc Bitoun, Valérie Biancalana, et al.
BMJ Open|July 21, 2021
Patient-reportedimpact of myasthenia gravis in the real world: protocol for a digital observational study (MyRealWorld MG)Sonia Berrih-Aknin, Kristl G Claeys, Nancy Law, et al.
European Journal of Medical Genetics|October 5, 2010
De novo RYR1 heterozygous mutation (I4898T) causing lethal core-rod myopathy in twinsAurelio Hernandez-Lain, Isabelle Husson, Nicole Monnier, et al.
BMJ Open|May 11, 2023
Patient-reported impact of myasthenia gravis in the real world: findings from a digital observational survey-based study (MyRealWorld MG)Sonia Berrih-Aknin, Jacqueline Palace, Andreas Meisel, et al.
Neuropathology and Applied Neurobiology|June 17, 2018
Serum neurofilament light chain levels as a marker of upper motor neuron degeneration in patients with Amyotrophic Lateral SclerosisB Gille, M De Schaepdryver, J Goossens, et al.
Pageof 24

Showing results (151-160 of 239) with videos related to

Sort By:
Pageof 24
Seizure|April 4, 2007
Epilepsy and migraine in a patient with Urbach-Wiethe diseaseKristl G Claeys, Lieve R F Claes, Johan W M Van Goethem, et al.
Neurology|April 27, 2007
Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9qL Deprez, K Peeters, W Van Paesschen, et al.
European Journal of Neurology|November 17, 2025
Novel Mutations in Titin Exon 363 With Different Phenotypes Including a Founder Mutation in Eastern EuropeVeronica Sian, Maria Francesca Di Feo, Sergei Kurbatov, et al.
Epilepsia|November 22, 2007
Epilepsy as part of the phenotype associated with ATP1A2 mutationsLiesbet Deprez, Sarah Weckhuysen, Katelijne Peeters, et al.
Human Mutation|December 21, 2020
Expanding the clinical and genetic spectrum of FDXR deficiency by functional validation of variants of uncertain significanceSarah L Stenton, Dorota Piekutowska-Abramczuk, Lea Kulterer, et al.
Acta Neuropathologica|December 17, 2008
"Necklace" fibers, a new histological marker of late-onset MTM1-related centronuclear myopathyJorge A Bevilacqua, Marc Bitoun, Valérie Biancalana, et al.
BMJ Open|July 21, 2021
Patient-reportedimpact of myasthenia gravis in the real world: protocol for a digital observational study (MyRealWorld MG)Sonia Berrih-Aknin, Kristl G Claeys, Nancy Law, et al.
European Journal of Medical Genetics|October 5, 2010
De novo RYR1 heterozygous mutation (I4898T) causing lethal core-rod myopathy in twinsAurelio Hernandez-Lain, Isabelle Husson, Nicole Monnier, et al.
BMJ Open|May 11, 2023
Patient-reported impact of myasthenia gravis in the real world: findings from a digital observational survey-based study (MyRealWorld MG)Sonia Berrih-Aknin, Jacqueline Palace, Andreas Meisel, et al.
Neuropathology and Applied Neurobiology|June 17, 2018
Serum neurofilament light chain levels as a marker of upper motor neuron degeneration in patients with Amyotrophic Lateral SclerosisB Gille, M De Schaepdryver, J Goossens, et al.
Pageof 24