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Keyword [SCN1A]
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1. Study Of The Spectrum Of Febrile Seizures Related Epilepsy And Its Possible Genetics
2. Mapping And Mutation Detection Of Causative Genes For Idiopathic Epilepsy Syndromes FCTE And BFIS, And Mutation Detection For GEFS+
3. The Pathogenesis Of Epilepsy Of SCN1A Mutation
4. Autism In Febrile Seizures Related Epilepsy: Prevalence, Features, And Relationship To The Clinical Characteristics Of Epilepsy, Mental Retardation And SCN1A Mutation
5. Clinical Analysis And Gene Mutation Screening Of SCN1B And SCN1A In Generalized Epilepsy With Febrile Seizures Plus Families
6. Clinical Analysis And Gene Mutation Screening Of SCN1A With Two Hereditary Epileptic Syndromes (GEFS~+ & Dravet Syndrome)
7. Study Of The Relationship Of SCN1A Genotype,Clinical Phenotype And The Effect Of Treatment In Severe Myoclonic Epilepsy In Infancy
8. The Influence Of Recurrent Febrile Seizures To The Brain Function In Scn1a Mutant Rats
9. The Hereditary Features Of Epilepsies With SCN1A Mutations
10. A Novel Scn1a Missense Mutation P. Leu193phe Associated With Gefs~+
11. MLPA Technique In The Application Of SCN1A Gene Research In Children With Fever Releated Seizures
12. Screen For SCN1A Mutations In Patients With Partial Epilepsy With FS Plus And Splicing Assay Of The Intronic Mutations In Vitro
13. Study On The Correlation Between SNP Of SCN1A And Epilepsia Genuina Of Four Peculiar Minorities In Yunnan Province
14. Altered Channel Preperties And Responses To Protein Kinases Modulation In Epilepsy-associated SCN1A Mutations
15. The Influence Of Gene Polymorphism On Pharmacokinetics And Pharmacodynamics Of Carbamazepine And Its Derivative Oxcarbazepine
16. The Role Of Scn1a Gene Variations In The Pathogenesis Of Familial Febrile Seizures
17. Generation Of The SCN1A Epilepsy Mutation In HiPS Cells Using The TALEN Technique
18. Genotype-phenotype Relationships In Genetic Epilepsy With Febrile Seizures Plus
19. Eeffect On SCN1A And GABA_A Receptor Subunits Polymorphisms For Efficacy And Safety Of Carbamazepine Monotherapy In Chinese Patients With Partial Seizures
20. Investigation On The Mechanism Of U1snRNA And Morpholino Correcting The Aberrant Splicing Of SCN1A Mutations
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