Marcin Bednarz

Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Cav1.1 mutation

Chunxiang Fan, Frank Lehmann‐Horn, Marc‐André Weber et al. · Brain · 2013 · 42 citations · Full text

<i>SCN4A</i>pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy

Alberto Bergareche, Marcin Bednarz, Elena Sánchez et al. · Human Molecular Genetics · 2015 · 42 citations · Full text

Genetics, Genetic Epidemiology, Molecular Biology +17

SCN4A Pore Mutation Pathogenetically Contributes to Autosomal Dominant Essential Tremor and May Increase Susceptibility to Epilepsy

Alberto Bergareche, Marcin Bednarz, Elena Sánchez et al. · Biophysical Journal · 2016 · 30 citations · Full text

Neurological Disorder, Genetics, Neuroscience +5

Wireless Local Area Networks Threat Detection Using 1D-CNN

Marek Natkaniec, Marcin Bednarz · Sensors · 2023 · 17 citations · Full text

A novel Ile1455Thr variant in the skeletal muscle sodium channel alpha-subunit in a patient with a severe adult-onset proximal myopathy with electrical myotonia and a patient with mild paramyotonia phenotype

Marcin Bednarz, Bas C. Stunnenberg, Benno Küsters et al. · Neuromuscular Disorders · 2016 · 11 citations

Channelopathies, Urology, Muscle Function +11