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Your search keyword '"Yendle, Simone"' showing total 10 results

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2. Mutations in KCNT1 cause a spectrum of focal epilepsies

3. Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome

5. Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers

6. KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy

7. Rare Copy Number Variants Are an Important Cause of Epileptic Encephalopathies

8. Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology

9. GRIN2A mutations cause epilepsy-aphasia spectrum disorders.

10. Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

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