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You searched for: Author/Creator Scheffer, Ingrid

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1. Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients. Issue 1 (December 2015)

2. Cultural relevance of the global impact of Dravet Syndrome in Australia, Italy, the US and UK. (June 2017)

3. Epilepsy with auditory features: A heterogeneous clinico-molecular disease. (June 2015)

4. Genome‐wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug‐resistant epilepsy. (16th July 2018)

6. Quinidine in the treatment of KCNT1‐positive epilepsies. Issue 6 (18th November 2015)