Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Marcin Bednarz

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Sensors (Basel, Switzerland)|July 8, 2023
Wireless Local Area Networks Threat Detection Using 1D-CNNMarek Natkaniec, Marcin Bednarz
Sensors (Basel, Switzerland)|January 25, 2025
Remote Radio Frequency Sensing Based on 5G New Radio Positioning Reference SignalsMarcin Bednarz, Tomasz P Zielinski
Brain : a Journal of Neurology|November 19, 2013
Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutationChunxiang Fan, Frank Lehmann-Horn, Marc-André Weber, et al.
Neuromuscular Disorders : NMD|December 28, 2016
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 phenotypeMarcin Bednarz, Bas C Stunnenberg, Benno Kusters, et al.
Human Molecular Genetics|October 3, 2015
SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsyAlberto Bergareche, Marcin Bednarz, Elena Sánchez, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Sensors (Basel, Switzerland)|July 8, 2023
Wireless Local Area Networks Threat Detection Using 1D-CNNMarek Natkaniec, Marcin Bednarz
Sensors (Basel, Switzerland)|January 25, 2025
Remote Radio Frequency Sensing Based on 5G New Radio Positioning Reference SignalsMarcin Bednarz, Tomasz P Zielinski
Brain : a Journal of Neurology|November 19, 2013
Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutationChunxiang Fan, Frank Lehmann-Horn, Marc-André Weber, et al.
Neuromuscular Disorders : NMD|December 28, 2016
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 phenotypeMarcin Bednarz, Bas C Stunnenberg, Benno Kusters, et al.
Human Molecular Genetics|October 3, 2015
SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsyAlberto Bergareche, Marcin Bednarz, Elena Sánchez, et al.
Pageof 1