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Phenotypic expansion of KCNH1‐associated disorders to include isolated epilepsy and its associations with genotypes and molecular sub‐regional locations.
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- CNS Neuroscience & Therapeutics, 2023, v. 29, n. 1, p. 270, doi. 10.1111/cns.14001
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- Article
The Characterization of Childhood Occipital Epilepsy of Gastaut: A Study of Seven Patients.
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- Cell Biochemistry & Biophysics, 2013, v. 67, n. 3, p. 991, doi. 10.1007/s12013-013-9594-8
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- Article
The increase of Nrf2 m6A modification induced by FTO downregulation promotes hippocampal neuron injury and aggravates the progression of epilepsy in a rat model.
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- Synapse, 2023, v. 77, n. 4, p. 1, doi. 10.1002/syn.22270
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- Article
Role of TRAK1 variants in epilepsy: genotype--phenotype analysis in a pediatric case of epilepsy with developmental disorder.
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- Frontiers in Molecular Neuroscience, 2024, p. 1, doi. 10.3389/fnmol.2024.1342371
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- Article
Joubert syndrome type 17 caused by c.650G > A and c.956A > T mutations in C5orf42 gene in children: one case report.
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- Chinese Journal of Contemporary Neurology & Neurosurgery, 2023, v. 23, n. 11, p. 1052, doi. 10.3969/j.issn.1672-6731.2023.11.015
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- Article
Research progress of nerve stimulation in the treatment of epilepsy in children.
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- Chinese Journal of Contemporary Neurology & Neurosurgery, 2021, v. 21, n. 8, p. 696, doi. 10.3969/j.issn.1672-6731.2021.08.014
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- Article