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

Fritz Zimprich

Showing results (71-80 of 103) with videos related to

Pageof 11
Sort By:
Journal of Neurology|October 29, 2022
The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide studyMartin Krenn, Merve Sener, Jakob Rath, et al.
Epilepsia|January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsyDennis Lal, Holger Trucks, Rikke S Møller, et al.
Therapeutic Advances in Neurological Disorders|December 28, 2023
Guideline for the management of myasthenic syndromesHeinz Wiendl, Angela Abicht, Andrew Chan, et al.
Plos One|August 28, 2018
Rare gene deletions in genetic generalized and Rolandic epilepsiesKamel Jabbari, Dheeraj R Bobbili, Dennis Lal, et al.
Neurology|September 26, 2025
Screening for Congenital Myasthenic Syndromes in Adults With Seronegative Myasthenia Gravis Using Next-Generation SequencingMartin Krenn, Matias Wagner, Helena Schuller, et al.
Annals of Clinical and Translational Neurology|May 21, 2021
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsyStefan Wolking, Claudia Moreau, Mark McCormack, et al.
European Journal of Neurology|March 3, 2022
Clinico-genetic spectrum of limb-girdle muscular weakness in Austria: A multicentre cohort studyMartin Krenn, Matthias Tomschik, Matias Wagner, et al.
Journal of Medical Genetics|July 31, 2017
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsiesEduardo Pérez-Palma, Ingo Helbig, Karl Martin Klein, et al.
Journal of Neurology|September 28, 2018
Multifocal motor neuropathy in Austria: a nationwide survey of clinical features and response to treatmentWolfgang N Löscher, Eva-Maria Oberreiter, Marcus Erdler, et al.
Neurology. Genetics|December 12, 2018
TPP2 mutation associated with sterile brain inflammation mimicking MSEva M Reinthaler, Elisabeth Graf, Tobias Zrzavy, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
Journal of Neurology|October 29, 2022
The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide studyMartin Krenn, Merve Sener, Jakob Rath, et al.
Epilepsia|January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsyDennis Lal, Holger Trucks, Rikke S Møller, et al.
Therapeutic Advances in Neurological Disorders|December 28, 2023
Guideline for the management of myasthenic syndromesHeinz Wiendl, Angela Abicht, Andrew Chan, et al.
Plos One|August 28, 2018
Rare gene deletions in genetic generalized and Rolandic epilepsiesKamel Jabbari, Dheeraj R Bobbili, Dennis Lal, et al.
Neurology|September 26, 2025
Screening for Congenital Myasthenic Syndromes in Adults With Seronegative Myasthenia Gravis Using Next-Generation SequencingMartin Krenn, Matias Wagner, Helena Schuller, et al.
Annals of Clinical and Translational Neurology|May 21, 2021
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsyStefan Wolking, Claudia Moreau, Mark McCormack, et al.
European Journal of Neurology|March 3, 2022
Clinico-genetic spectrum of limb-girdle muscular weakness in Austria: A multicentre cohort studyMartin Krenn, Matthias Tomschik, Matias Wagner, et al.
Journal of Medical Genetics|July 31, 2017
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsiesEduardo Pérez-Palma, Ingo Helbig, Karl Martin Klein, et al.
Journal of Neurology|September 28, 2018
Multifocal motor neuropathy in Austria: a nationwide survey of clinical features and response to treatmentWolfgang N Löscher, Eva-Maria Oberreiter, Marcus Erdler, et al.
Neurology. Genetics|December 12, 2018
TPP2 mutation associated with sterile brain inflammation mimicking MSEva M Reinthaler, Elisabeth Graf, Tobias Zrzavy, et al.
Pageof 11