Matthias K. Bernhard

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

Steffen Syrbe, Ulrike B. S. Hedrich, Erik Riesch et al. · Nature Genetics · 2015 · 275 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study

Afshin Saffari, Ines Brösse, Adelheid Wiemer‐Kruel et al. · Orphanet Journal of Rare Diseases · 2019 · 126 citations · Full text

Medicine, Neurology, Pediatrics +17

47 patients with FLNA associated periventricular nodular heterotopia

Max Lange, Burkhard S. Kasper, Axel Bohring et al. · Orphanet Journal of Rare Diseases · 2015 · 106 citations · Full text

Life Sciences, Genetics, Neurology +17

Expression of purinergic receptors (ionotropic P2X1–7 and metabotropic P2Y1–11) during myeloid differentiation of HL60 cells

Kathrin Adrian, Matthias K. Bernhard, Hans‐Georg Breitinger et al. · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · 2000 · 79 citations

Life Sciences, Cell Biology, Pharmacology +8

Use of complementary and alternative medicine (CAM) by parents in their children and adolescents with epilepsy – Prevelance, predictors and parents' assessment

Nicole Hartmann, Martina Patrizia Neininger, Matthias K. Bernhard et al. · European Journal of Paediatric Neurology · 2015 · 56 citations

Medicine, Child Health, Pediatrics +8