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 (61-70 of 103) with videos related to

Pageof 11
Sort By:
Plos One|September 24, 2010
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizuresSarah Jamali, Annick Salzmann, Nader Perroud, et al.
Neurology. Genetics|May 9, 2025
Holistic Exome-Based Genetic Testing in Adults With EpilepsyMartin Krenn, Matias Wagner, Karin Trimmel, et al.
Journal of Autoimmunity|March 1, 2024
Impact of muscle biopsy on the clinical decision-making process in patients with suspected idiopathic inflammatory myopathyKastriot Kastrati, Nasim Nakhost Lotfi, Marwa G Tawfik, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 22, 2020
ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment responseMarius Gasser, Ponghatai Boonsimma, Wiracha Netbaramee, et al.
Epilepsia|July 5, 2014
Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsyEva M Reinthaler, Dennis Lal, Wiktor Jurkowski, et al.
Journal of Neurology|January 9, 2026
Demographic, clinical and genetic characteristics of patients with amyotrophic lateral sclerosis from two specialised centres in AustriaOmar Keritam, Vera Elisabeth Kleinveld, Sigrid Klotz, et al.
Annals of Neurology|January 24, 2022
B Cell Depletion and SARS-CoV-2 Vaccine Responses in Neuroimmunologic PatientsBarbara Kornek, Fritz Leutmezer, Paulus S Rommer, et al.
Journal of Neurology|December 21, 2023
Next-generation sequencing and comprehensive data reassessment in 263 adult patients with neuromuscular disorders: insights into the gray zone of molecular diagnosesMartin Krenn, Matias Wagner, Gudrun Zulehner, et al.
Muscle & Nerve|February 9, 2024
Multifocal motor neuropathy as a mimic of amyotrophic lateral sclerosis: Serum neurofilament light chain as a reliable diagnostic biomarkerVera E A Kleinveld, Omar Keritam, Corinne G C Horlings, et al.
Annals of Neurology|March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhoodDennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Pageof 11

Showing results (61-70 of 103) with videos related to

Sort By:
Pageof 11
Plos One|September 24, 2010
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizuresSarah Jamali, Annick Salzmann, Nader Perroud, et al.
Neurology. Genetics|May 9, 2025
Holistic Exome-Based Genetic Testing in Adults With EpilepsyMartin Krenn, Matias Wagner, Karin Trimmel, et al.
Journal of Autoimmunity|March 1, 2024
Impact of muscle biopsy on the clinical decision-making process in patients with suspected idiopathic inflammatory myopathyKastriot Kastrati, Nasim Nakhost Lotfi, Marwa G Tawfik, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 22, 2020
ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment responseMarius Gasser, Ponghatai Boonsimma, Wiracha Netbaramee, et al.
Epilepsia|July 5, 2014
Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsyEva M Reinthaler, Dennis Lal, Wiktor Jurkowski, et al.
Journal of Neurology|January 9, 2026
Demographic, clinical and genetic characteristics of patients with amyotrophic lateral sclerosis from two specialised centres in AustriaOmar Keritam, Vera Elisabeth Kleinveld, Sigrid Klotz, et al.
Annals of Neurology|January 24, 2022
B Cell Depletion and SARS-CoV-2 Vaccine Responses in Neuroimmunologic PatientsBarbara Kornek, Fritz Leutmezer, Paulus S Rommer, et al.
Journal of Neurology|December 21, 2023
Next-generation sequencing and comprehensive data reassessment in 263 adult patients with neuromuscular disorders: insights into the gray zone of molecular diagnosesMartin Krenn, Matias Wagner, Gudrun Zulehner, et al.
Muscle & Nerve|February 9, 2024
Multifocal motor neuropathy as a mimic of amyotrophic lateral sclerosis: Serum neurofilament light chain as a reliable diagnostic biomarkerVera E A Kleinveld, Omar Keritam, Corinne G C Horlings, et al.
Annals of Neurology|March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhoodDennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Pageof 11