Epilepsy in Dravet Syndrome—Current and Future Therapeutic Opportunities.
- Published in:
- Journal of Clinical Medicine, 2023, v. 12, n. 7, p. 2532, doi. 10.3390/jcm12072532
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- Publication type:
- Article
Works by Mei, Daoqi
Results: 13
1
2
Subependymal Giant Cell Astrocytomas in Tuberous Sclerosis Complex—Current Views on Their Pathogenesis and Management.
- Published in:
- Journal of Clinical Medicine, 2023, v. 12, n. 3, p. 956, doi. 10.3390/jcm12030956
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- Publication type:
- Article
3
Ketogenic Diet Therapy for Drug-Resistant Epilepsy and Cognitive Impairment in Children With Tuberous Sclerosis Complex.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.863826
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- Publication type:
- Article
4
Neuronal Nitric Oxide Synthase Knockdown Within Basolateral Amygdala Induces Autistic-Related Phenotypes and Decreases Excitatory Synaptic Transmission in Mice.
- Published in:
- Frontiers in Neuroscience, 2020, v. 14, p. N.PAG, doi. 10.3389/fnins.2020.00886
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- Publication type:
- Article
5
Neuroprotective Effects of CXCR2 Antagonist SB332235 on Traumatic Brain Injury Through Suppressing NLRP3 Inflammasome.
- Published in:
- Neurochemical Research, 2024, v. 49, n. 1, p. 184, doi. 10.1007/s11064-023-04021-8
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- Publication type:
- Article
6
The GluN2B-Trp373 NMDA Receptor Variant is Associated with Autism-, Epilepsy-Related Phenotypes and Reduces NMDA Receptor Currents in Rats.
- Published in:
- Neurochemical Research, 2022, v. 47, n. 6, p. 1588, doi. 10.1007/s11064-022-03554-8
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- Publication type:
- Article
7
Case report: Second report of neuromuscular syndrome caused by biallelic variants in ASCC3.
- Published in:
- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1382275
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- Publication type:
- Article
8
Clinical and genetic analysis of benign familial infantile epilepsy caused by PRRT2 gene variant.
- Published in:
- Frontiers in Neurology, 2023, p. 1, doi. 10.3389/fneur.2023.1135044
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- Publication type:
- Article
9
Evaluating the relationship between the proportion of X-chromosome deletions and clinical manifestations in children with turner syndrome.
- Published in:
- Frontiers in Endocrinology, 2024, p. 1, doi. 10.3389/fendo.2024.1324160
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- Publication type:
- Article
10
Genetic analysis of four cases of Poirier Bienvenu neurodevelopmental syndrome associated with CSNK2B variant.
- Published in:
- BMC Medical Genomics, 2025, v. 18, n. 1, p. 1, doi. 10.1186/s12920-025-02132-5
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- Publication type:
- Article
11
Restoration of nNOS Expression Rescues Autistic-Like Phenotypes Through Normalization of AMPA Receptor-Mediated Neurotransmission.
- Published in:
- Molecular Neurobiology, 2024, v. 61, n. 9, p. 6599, doi. 10.1007/s12035-024-03997-w
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- Publication type:
- Article
12
Somatostatin-expressing interneurons of prefrontal cortex modulate social deficits in the Magel2 mouse model of autism.
- Published in:
- Molecular Autism, 2025, v. 16, n. 1, p. 1, doi. 10.1186/s13229-025-00653-5
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- Publication type:
- Article
13
Exons deletion of CNKSR2 gene identified in X-linked syndromic intellectual disability.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01004-2
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- Publication type:
- Article