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You searched for: Author/Creator Becker, Felicitas

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2. ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation. (June 2017)

3. Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation. Issue 3 (13th February 2016)

5. Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy. Issue 3 (4th July 2019)

6. Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis. (31st August 2017)

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

8. Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy. (15th July 2015)

9. Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy. Issue 3 (5th August 2017)

10. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. (23rd January 2018)