Found: 19
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Genetic etiologies of the electrical status epilepticus during slow wave sleep: systematic review.
- Published in:
- BMC Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12863-018-0628-5
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- Publication type:
- Article
The Study of Genetic Susceptibility and Mitochondrial Dysfunction in Mesial Temporal Lobe Epilepsy.
- Published in:
- Molecular Neurobiology, 2020, v. 57, n. 9, p. 3920, doi. 10.1007/s12035-020-01993-4
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- Publication type:
- Article
Myelin Oligodendrocyte Glycoprotein (MOG) Antibody Diseases in Children in Central South China: Clinical Features, Treatments, Influencing Factors, and Outcomes.
- Published in:
- Frontiers in Neurology, 2019, p. 1, doi. 10.3389/fneur.2019.00868
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- Publication type:
- Article
Next‐generation sequencing improves treatment efficacy and reduces hospitalization in children with drug‐resistant epilepsy.
- Published in:
- CNS Neuroscience & Therapeutics, 2019, v. 25, n. 1, p. 14, doi. 10.1111/cns.12869
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- Publication type:
- Article
Genotype-phenotype correlations of STXBP1 pathogenic variants and the treatment choices for STXBP1-related disorders in China.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01474-2
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- Publication type:
- Article
A Case With 4 de Novo Copy Number Variations With Clinical Features That Overlap 1q43q44 Microdeletion and 3q29 Microduplication Syndromes.
- Published in:
- Child Neurology Open, 2018, v. 5, p. 1, doi. 10.1177/2329048X18798200
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- Publication type:
- Article
De Novo KCNQ2 Mutation in One Case of Epilepsy of Infancy With Migrating Focal Seizures That Evolved to Infantile Spasms.
- Published in:
- Child Neurology Open, 2018, v. 5, p. 1, doi. 10.1177/2329048X18767738
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- Publication type:
- Article
The patterns of response of 11 regimens for infantile spasms.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-68403-6
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- Publication type:
- Article
Restoration of Sarco/Endoplasmic Reticulum Ca<sup>2+</sup>-ATPase Activity Functions as a Pivotal Therapeutic Target of Anti-Glutamate-Induced Excitotoxicity to Attenuate Endoplasmic Reticulum Ca<sup>2+</sup> Depletion.
- Published in:
- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.877175
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- Publication type:
- Article
Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy.
- Published in:
- Frontiers in Neurology, 2018, p. N.PAG, doi. 10.3389/fneur.2018.00947
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- Publication type:
- Article
Editorial: 90th anniversary of the 1932 Sherrington and Adrian Nobel prize: molecular pathways of synaptic transmission regulation.
- Published in:
- Frontiers in Molecular Neuroscience, 2023, p. 01, doi. 10.3389/fnmol.2023.1271369
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- Publication type:
- Article
The genotype–phenotype correlations of the CACNA1A-related neurodevelopmental disorders: a small case series and literature reviews.
- Published in:
- Frontiers in Molecular Neuroscience, 2023, p. 1, doi. 10.3389/fnmol.2023.1222321
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- Publication type:
- Article
Disruption of mitochondrial and lysosomal functions by human CACNA1C variants expressed in HEK 293 and CHO cells.
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- Frontiers in Molecular Neuroscience, 2023, p. 1, doi. 10.3389/fnmol.2023.1209760
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- Publication type:
- Article
Intellectual Disability and Potassium Channelopathies: A Systematic Review.
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- Frontiers in Genetics, 2020, v. 11, p. 1, doi. 10.3389/fgene.2020.00614
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- Publication type:
- Article
Attention-deficit/hyperactive disorder updates.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.925049
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- Publication type:
- Article
The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic Review.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.807202
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- Publication type:
- Article
Calcium channelopathies and intellectual disability: a systematic review.
- Published in:
- 2021
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- Publication type:
- journal article
Treatment for the Benign Childhood Epilepsy With Centrotemporal Spikes: A Monocentric Study.
- Published in:
- Frontiers in Neurology, 2021, v. 11, p. N.PAG, doi. 10.3389/fneur.2021.670958
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- Publication type:
- Article
Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patients.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01028-4
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- Publication type:
- Article