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Pyridoxine dependent epilepsies: new therapeutical point of view

Pyridoxine dependent epilepsies (PDEs) are rare autosomal recessive disorders with onset in neonatal period. Seizures are typically not responsive to conventional antiepileptic drugs, but they cease after parental pyridoxine administration. Atypical forms are characterized partly response to pyridox...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Ital J Pediatr
Prif Awduron: Falsaperla, Raffaele, Corsello, Giovanni
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2017
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5545091/
https://ncbi.nlm.nih.gov/pubmed/28779752
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13052-017-0387-3
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