Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marcin Bednarz"'
Autor:
Marek Natkaniec, Marcin Bednarz
Publikováno v:
Sensors, Vol 23, Iss 12, p 5507 (2023)
Wireless Local Area Networks (WLANs) have revolutionized modern communication by providing a user-friendly and cost-efficient solution for Internet access and network resources. However, the increasing popularity of WLANs has also led to a rise in se
Externí odkaz:
https://doaj.org/article/62a13cee748147398f98b49e13becf88
Autor:
Yuwei Da, Karin Jurkat-Rott, Marcin Bednarz, Frank Lehmann-Horn, Jens Schallner, Chunxiang Fan
Publikováno v:
Journal of Neurological Research And Therapy. 1:20-30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::097695c27586f13de65a424c7ecfd36f
https://doi.org/10.14302/issn.2470-5020.jnrt-16-993
https://doi.org/10.14302/issn.2470-5020.jnrt-16-993
Autor:
Marcin Bednarz, Frank Lehmann-Horn, Marc-André Weber, James R. Groome, Chunxiang Fan, Karin Jurkat-Rott, Malin K.B. Jonsson
Publikováno v:
Brain
We studied a two-generation family presenting with conditions that included progressive permanent weakness, myopathic myopathy, exercise-induced contracture before normokalaemic periodic paralysis or, if localized to the tibial anterior muscle group,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8da6a2a5dacda3c82fc68fc4b1b59fbc
http://europepmc.org/articles/PMC3859226
http://europepmc.org/articles/PMC3859226
Autor:
James R. Groome, Nicol C. Voermans, Giovanni Meola, Christiaan G J Saris, Erik-Jan Kamsteeg, Bas C. Stunnenberg, Benno Küsters, Marcin Bednarz, Vern Winston, Karin Jurkat-Rott
Publikováno v:
Neuromuscular Disorders, 27, 2, pp. 175-182
Neuromuscular Disorders, 27, 175-182
Neuromuscular Disorders, 27, 175-182
Item does not contain fulltext In sodium channelopathies, a severe fixed myopathy caused by a dominant mutation is rare. We describe two unrelated patients with a novel variant, p.Ile1455Thr, with phenotypes of paramyotonia in one case and fixed prox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b2b8be7f556781dba8124c855eb85b8
https://pubmed.ncbi.nlm.nih.gov/28024841
https://pubmed.ncbi.nlm.nih.gov/28024841
Autor:
Coro Paisán-Ruiz, Ana Gorostidi, Elena Sánchez, Catharine E. Krebs, Karin Jurkat-Rott, Alberto Bergareche, Marcin Bednarz, Jose Felix Marti-Masso, Patricia de la Riva, Vladimir Makarov, Javier Ruiz-Martínez
Essential tremor (ET) is the most prevalent movement disorder, affecting millions of people in the USA. Although a positive family history is one of the most important risk factors for ET, the genetic causes of ET remain unknown. In an attempt to ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::873ecae006596c2bd6e2fc5549dab5c0
https://europepmc.org/articles/PMC4654061/
https://europepmc.org/articles/PMC4654061/
Publikováno v:
Biophysical Journal. 104:295a
Hypokalemic periodic paralysis (HypoPP) is the most common form of the periodic paralysis. It is caused by mutations in two voltage-gated ion channels of skeletal muscle, Cav1.1 (HypoPP-1) and Nav1.4 (HypoPP-2). Almost all HypoPP-causing mutations re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47b91e0dd52a0a827e504d8ef388a836
https://doi.org/10.1016/j.bpj.2012.11.1648
https://doi.org/10.1016/j.bpj.2012.11.1648