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Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutation

Wissenschaftlicher Artikel

Fan, Chunxiang; Lehmann-Horn, Frank; Weber, Marc-Andre; Bednarz, Marcin; Groome, James R.; Jonsson, Malin K. B.; Jurkat-Rott, Karin (Universität Ulm, 2013)

SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy

Wissenschaftlicher Artikel

Bergareche, Alberto; Bednarz, Marcin; Sanchez, Elena; Krebs, Catharine E.; Ruiz-Martinez, Javier; De La Riva, Patricia; Makarov, Vladimir; Gorostidi, Ana; Jurkat-Rott, Karin; Felix Marti-Masso, Jose; Paisan-Ruiz, Coro (Universität Ulm, 2015)

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