15 results on '"Zuberi, S. M."'
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2. The Differential Diagnosis of Epilepsy
3. The Differential Diagnosis of Epilepsy
4. Chipping away at the channels: Can we fashion a syndrome?
5. Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome
6. Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology
7. Genotype-phenotype associations in SCN1A-related epilepsies
8. Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins
9. De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin
10. Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures
11. Current topic: Ion channels and neurology
12. Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability
13. A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy
14. Hyperammonaemic encephalopathy after a subureteric injection for vesicoureteric reflux
15. "Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndrome.
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