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Atay Vural

Showing results (51-60 of 58) with videos related to

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Cell Reports. Medicine|May 19, 2026
Synaptophysin autoantibodies mediate synaptic dysfunction in cerebellar ataxiaSamantha Ho, Hoi Kiu Wong, Dorina Shqau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2025
Spastic Ataxia Composite (SPAXCOM): A Scale to Evaluate the Progression of Subjects with Spasticity and AtaxiaCécile Di Folco, Charlotte Dubec-Fleury, Andreas Traschütz, et al.
Pediatric Neurology|May 28, 2023
Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter StudyGamze Sarıkaya Uzan, Atay Vural, Deniz Yüksel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2022
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar AtaxiaLiedewei Van de Vondel, Jonathan De Winter, Danique Beijer, et al.
Biorxiv : the Preprint Server for Biology|December 9, 2024
Sex-specific DNA methylation differences in Amyotrophic lateral sclerosisOlivia A Grant, Alfredo Iacoangeli, Ramona A J Zwamborn, et al.
Frontiers in Cellular Neuroscience|January 2, 2023
Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence dataAhmad Al Khleifat, Alfredo Iacoangeli, Ashley R Jones, et al.
NPJ Genomic Medicine|January 29, 2022
Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosisAhmad Al Khleifat, Alfredo Iacoangeli, Joke J F A van Vugt, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 24, 2021
The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical PracticeAtay Vural, Gülşah Şimşir, Şeyma Tekgül, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Cell Reports. Medicine|May 19, 2026
Synaptophysin autoantibodies mediate synaptic dysfunction in cerebellar ataxiaSamantha Ho, Hoi Kiu Wong, Dorina Shqau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2025
Spastic Ataxia Composite (SPAXCOM): A Scale to Evaluate the Progression of Subjects with Spasticity and AtaxiaCécile Di Folco, Charlotte Dubec-Fleury, Andreas Traschütz, et al.
Pediatric Neurology|May 28, 2023
Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter StudyGamze Sarıkaya Uzan, Atay Vural, Deniz Yüksel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2022
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar AtaxiaLiedewei Van de Vondel, Jonathan De Winter, Danique Beijer, et al.
Biorxiv : the Preprint Server for Biology|December 9, 2024
Sex-specific DNA methylation differences in Amyotrophic lateral sclerosisOlivia A Grant, Alfredo Iacoangeli, Ramona A J Zwamborn, et al.
Frontiers in Cellular Neuroscience|January 2, 2023
Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence dataAhmad Al Khleifat, Alfredo Iacoangeli, Ashley R Jones, et al.
NPJ Genomic Medicine|January 29, 2022
Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosisAhmad Al Khleifat, Alfredo Iacoangeli, Joke J F A van Vugt, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 24, 2021
The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical PracticeAtay Vural, Gülşah Şimşir, Şeyma Tekgül, et al.
Pageof 6