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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...
Αποθηκεύτηκε σε:
Τόπος έκδοσης: | Biomedicine (Taipei) |
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Κύριοι συγγραφείς: | , , , , , , |
Μορφή: | Artigo |
Γλώσσα: | Inglês |
Έκδοση: |
China Medical University
2014
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Θέματα: | |
Διαθέσιμο Online: | 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 |
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