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Concurrent Quinidine and Phenobarbital in the Treatment of a Patient with 2 KCNT1 Mutations
Epilepsy of infancy with migrating focal seizures is a devastating pediatric neurologic disorder that often results in treatment-resistant seizure activity and developmental delay. The condition has been associated with mutations in the KCNT1 gene that cause a gain of function in neuronal sodium-act...
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| Yayımlandı: | Curr Ther Res Clin Exp |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Elsevier
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6677567/ https://ncbi.nlm.nih.gov/pubmed/31388363 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.curtheres.2019.02.002 |
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