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An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder

We report a three generation pedigree with 11 of 22 affected with a variant form of rolandic epilepsy, speech impairment, oromotor apraxia, and cognitive deficit. The core features comprised nocturnal rolandic seizures, interictal centrotemporal spike waves with early age of onset and late age of of...

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Detaylı Bibliyografya
Asıl Yazarlar: Kugler, Steven L., Bali, Bhavna, Lieberman, Philip, Strug, Lisa, Gagnon, Bernadine, Murphy, Peregrine L., Clarke, Tara, Greenberg, David A., Pal, Deb K.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2435390/
https://ncbi.nlm.nih.gov/pubmed/18248446
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1528-1167.2007.01517.x
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