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T. Bast

University of Freiburg

31

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165

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Clinical and genetic spectrum of SCN2A-associated episodic ataxia

2019 European Journal of Paediatric Neurology
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Structural brain anomalies in patients with FOXG 1 syndrome and in Foxg1+/− mice

2019 Annals of clinical and translational neurology
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Long-term seizure outcome in pediatric patients with focal cortical dysplasia undergoing tailored and standard surgical resections

2018 Seizure-european Journal of Epilepsy
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PND78 - SOCIO-ECONOMIC IMPACT OF DRAVET SYNDROME IN GERMANY: A REAL-WORLD STUDY

2018 Value in Health
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Benign epilepsy with centrotemporal spikes: Correlating spike frequency and neuropsychology

2018 Acta Neurologica Scandinavica
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In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

2016 Neuropediatrics
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Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5-related epilepsy

2016 European Journal of Paediatric Neurology
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Genotype and phenotype in GNAO1-Mutation – Case report of an unusual course of a childhood epilepsy

2016 Neuropediatrics
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Therapy and Clinical Course in 52 Patients with PCDH19 Mutations

2015 Neuropediatrics
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Intravenous levetiracetam in clinical practice – Results from an independent registry

2015 Seizure-european Journal of Epilepsy
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