טוען...
Successful control with carbamazepine of family with paroxysmal kinesigenic dyskinesia of PRRT2 mutation
Paroxysmal kinesigenic dyskinesia (PKD), a rare paroxysmal movement disorder often misdiagnosed as epilepsy, is characterized by recurrent, brief dyskinesia attacks triggered by sudden voluntary movement. Pathophysiological mechanism of PKD remains not well understood. Ion channelopathy has been sug...
שמור ב:
הוצא לאור ב: | Biomedicine (Taipei) |
---|---|
Main Authors: | , , , , , , |
פורמט: | Artigo |
שפה: | Inglês |
יצא לאור: |
China Medical University
2014
|
נושאים: | |
גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4265013/ https://ncbi.nlm.nih.gov/pubmed/25520928 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7603/s40681-014-0015-0 |
תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|