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You searched for: Author/Creator Kluger, Gerhard

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1. 47 patients with FLNA associated periventricular nodular heterotopia. Issue 1 (December 2015)

3. Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany. (May 2019)

4. Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 cases. (February 2019)

5. Clinical features and blood iron metabolism markers in children with beta-propeller protein associated neurodegeneration. (September 2020)

6. Co‐occurring malformations of cortical development and SCN1A gene mutations. Issue 7 (5th June 2014)

7. DEPDC5 mutations in genetic focal epilepsies of childhood. Issue 5 (14th April 2014)

10. Effectiveness of antiepileptic therapy in patients with PCDH19 mutations. (February 2016)