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Inflammation in epileptic encephalopathies
West syndrome (WS) is an infantile epileptic encephalopathy (EE) that manifests with infantile spasms, hypsarrhythmia (in ~60% of infants) and poor neurodevelopmental outcomes. The etiologies of WS can be structural-metabolic pathologies (~60%), genetic (12–15%) or of unknown origin. The current tre...
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| Pubblicato in: | Adv Protein Chem Struct Biol |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5753773/ https://ncbi.nlm.nih.gov/pubmed/28427564 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/bs.apcsb.2017.01.005 |
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