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Keyword [Dravet syndrome]
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1. The Pathogenesis Of Epilepsy Of SCN1A Mutation
2. Autism In Febrile Seizures Related Epilepsy: Prevalence, Features, And Relationship To The Clinical Characteristics Of Epilepsy, Mental Retardation And SCN1A Mutation
3. Clinical Analysis And Gene Mutation Screening Of SCN1A With Two Hereditary Epileptic Syndromes (GEFS~+ & Dravet Syndrome)
4. Clinical Features And NMD Mechanisms Of Truncation Mutants In SCN1A Gene
5. Relationship Between SCN1A Gene Mutation And Drug Efficacy In Chinese Families With Genetic Epilepsy With Febrile Seizures Plus
6. Stiripentol As An Adjuvant Therapy For Dravet Syndrome:A Meta-analysis Of Effectiveness And Safety
7. Functional Analysis Of The Mutation About The Sodium Channel Gene SCN1A 3' Untranslated Region (c.*20A>G) Related To The Dravet Syndrome
8. Early Clinical Characteristics Of Dravet Syndrome And Analysis For Gene Mutation Screening
9. Study On The Relationship Between The Mutation Characteristics Of SCN1A Gene In Dravet Syndrome And Its Clinical Phenotype
10. Genetic And Phenotypic Characteristics Of SCN1A-related Epilepsy
11. Neuroprotective Effect And Mechanism Of GLP-1 Analogue Liraglutide In Scn1a Gene Knockout Epilepsy Mice Model
12. Vagus Nerve Stimulation For Epileptic Encephalopathy In Children With Long-Term Follow-Up
13. Function And Mechanism Of Neddylation Of Na_v1.1 In The Excitability Of Interneurons And Seizure Prevention
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