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Miriam Kessi

Showing results (1-10 of 41) with videos related to

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Developmental Medicine and Child Neurology|September 4, 2025
Genetic etiologies of the infantile epileptic spasms syndrome: What do we know so far?Miriam Kessi, Lifen Yang
Current Neuropharmacology|April 20, 2026
Potassium Channelopathies and Precision Medicine Approaches in Epilepsy: A Systematic Review of Personalized Treatment StrategiesChangning Xie, Fei Yin, Miriam Kessi, et al.
Molecular Neurobiology|March 22, 2024
Roles of KCNA2 in Neurological Diseases: from Physiology to PathologyChangning Xie, Miriam Kessi, Fei Yin, et al.
Child Neurology Open|April 25, 2018
De Novo KCNQ2 Mutation in One Case of Epilepsy of Infancy With Migrating Focal Seizures That Evolved to Infantile SpasmsHaolin Duan, Jing Peng, Miriam Kessi, et al.
Current Neuropharmacology|June 2, 2026
Systematic Reviews and Meta-Analyses of the Use of Tocilizumab in Treating Central Nervous DiseasesJing Peng, Miriam Kessi, Fei Yin, et al.
Orphanet Journal of Rare Diseases|October 28, 2025
GRIN2B-related neurodevelopmental disorders: genotype-phenotype correlations and therapeutic implicationsChangning Xie, Miriam Kessi, Fangyun Liu, et al.
Neuroscience|September 12, 2025
Functional characterization and in vitro pharmacological rescue of a novel KCNA2 variant associated with developmental and epileptic encephalopathyChangning Xie, Miriam Kessi, Fang He, et al.
Orphanet Journal of Rare Diseases|May 14, 2021
Calcium channelopathies and intellectual disability: a systematic reviewMiriam Kessi, Baiyu Chen, Jing Peng, et al.
Child Neurology Open|September 29, 2018
A Case With 4 de Novo Copy Number Variations With Clinical Features That Overlap 1q43q44 Microdeletion and 3q29 Microduplication SyndromesMiriam Kessi, Jing Peng, Lifen Yang, et al.
Italian Journal of Pediatrics|February 7, 2025
The utilization of the multimodal immunotherapy for the opsoclonus-myoclonus syndrome can reduce relapses and permanent neurological sequelaeFang He, Miriam Kessi, Ciliu Zhang, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Developmental Medicine and Child Neurology|September 4, 2025
Genetic etiologies of the infantile epileptic spasms syndrome: What do we know so far?Miriam Kessi, Lifen Yang
Current Neuropharmacology|April 20, 2026
Potassium Channelopathies and Precision Medicine Approaches in Epilepsy: A Systematic Review of Personalized Treatment StrategiesChangning Xie, Fei Yin, Miriam Kessi, et al.
Molecular Neurobiology|March 22, 2024
Roles of KCNA2 in Neurological Diseases: from Physiology to PathologyChangning Xie, Miriam Kessi, Fei Yin, et al.
Child Neurology Open|April 25, 2018
De Novo KCNQ2 Mutation in One Case of Epilepsy of Infancy With Migrating Focal Seizures That Evolved to Infantile SpasmsHaolin Duan, Jing Peng, Miriam Kessi, et al.
Current Neuropharmacology|June 2, 2026
Systematic Reviews and Meta-Analyses of the Use of Tocilizumab in Treating Central Nervous DiseasesJing Peng, Miriam Kessi, Fei Yin, et al.
Orphanet Journal of Rare Diseases|October 28, 2025
GRIN2B-related neurodevelopmental disorders: genotype-phenotype correlations and therapeutic implicationsChangning Xie, Miriam Kessi, Fangyun Liu, et al.
Neuroscience|September 12, 2025
Functional characterization and in vitro pharmacological rescue of a novel KCNA2 variant associated with developmental and epileptic encephalopathyChangning Xie, Miriam Kessi, Fang He, et al.
Orphanet Journal of Rare Diseases|May 14, 2021
Calcium channelopathies and intellectual disability: a systematic reviewMiriam Kessi, Baiyu Chen, Jing Peng, et al.
Child Neurology Open|September 29, 2018
A Case With 4 de Novo Copy Number Variations With Clinical Features That Overlap 1q43q44 Microdeletion and 3q29 Microduplication SyndromesMiriam Kessi, Jing Peng, Lifen Yang, et al.
Italian Journal of Pediatrics|February 7, 2025
The utilization of the multimodal immunotherapy for the opsoclonus-myoclonus syndrome can reduce relapses and permanent neurological sequelaeFang He, Miriam Kessi, Ciliu Zhang, et al.
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