17 results on '"Yendle, Simone"'
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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
4. Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies
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. Mutations in KCNT1 cause a spectrum of focal epilepsies
10. Mutations inKCNT1cause a spectrum of focal epilepsies
11. Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers
12. Rare copy number variants are an important cause of epileptic encephalopathies
13. GRIN2A mutations cause epilepsy-aphasia spectrum disorders
14. Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
15. Mutations inPRRT2are not a common cause of infantile epileptic encephalopathies
16. Reduction of seizure frequency after epilepsy surgery in a patient withSTXBP1encephalopathy and clinical description of six novel mutation carriers
17. Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies
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