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Plos One
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September 24, 2010
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures
Sarah Jamali, Annick Salzmann, Nader Perroud, et al.
Neurology. Genetics
|
May 9, 2025
Holistic Exome-Based Genetic Testing in Adults With Epilepsy
Martin 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 myopathy
Kastriot 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 response
Marius Gasser, Ponghatai Boonsimma, Wiracha Netbaramee, et al.
Epilepsia
|
July 5, 2014
Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy
Eva 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 Austria
Omar 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 Patients
Barbara 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 diagnoses
Martin 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 biomarker
Vera E A Kleinveld, Omar Keritam, Corinne G C Horlings, et al.
Annals of Neurology
|
March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhood
Dennis Lal, Eva M Reinthaler, Julian Schubert, et al.
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of 11
Search research articles
Search
Showing results (61-70 of 103) with videos related to
Sort By:
Page
of 11
Plos One
|
September 24, 2010
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures
Sarah Jamali, Annick Salzmann, Nader Perroud, et al.
Neurology. Genetics
|
May 9, 2025
Holistic Exome-Based Genetic Testing in Adults With Epilepsy
Martin 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 myopathy
Kastriot 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 response
Marius Gasser, Ponghatai Boonsimma, Wiracha Netbaramee, et al.
Epilepsia
|
July 5, 2014
Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy
Eva 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 Austria
Omar 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 Patients
Barbara 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 diagnoses
Martin 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 biomarker
Vera E A Kleinveld, Omar Keritam, Corinne G C Horlings, et al.
Annals of Neurology
|
March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhood
Dennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Page
of 11