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You searched for: Author/Creator Mulley, John C.

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1. Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH123. Issue 1 (26th November 2012)

2. Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome. (15th May 2015)

3. Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome. (15th May 2015)

4. Multiplex families with epilepsy: Success of clinical and molecular genetic characterization. (23rd February 2016)

5. Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome. Issue 9 (29th July 2013)