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Marka van Blitterswijk

Showing results (31-40 of 89) with videos related to

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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 3, 2013
Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementiaMarka van Blitterswijk, Matthew C Baker, Kevin F Bieniek, et al.
Neurobiology of Aging|February 15, 2012
Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patientsMarka van Blitterswijk, Anna Blokhuis, Michael A van Es, et al.
Brain Pathology (Zurich, Switzerland)|July 11, 2024
Upper motor neuron-predominant motor neuron disease presenting as atypical parkinsonism: A clinicopathological studyAya Murakami, Shunsuke Koga, Shinsuke Fujioka, et al.
Biorxiv : the Preprint Server for Biology|July 16, 2025
Expanding the spectrum of annexin A11 proteinopathy in frontotemporal lobar degeneration and motor neuron diseaseNikhil B Ghayal, Richard J Crook, Angita Jain, et al.
Plos One|November 17, 2012
Genetic overlap between apparently sporadic motor neuron diseasesMarka van Blitterswijk, Lotte Vlam, Michael A van Es, et al.
Molecular Neurodegeneration|February 1, 2020
Elevated methylation levels, reduced expression levels, and frequent contractions in a clinical cohort of C9orf72 expansion carriersJazmyne L Jackson, NiCole A Finch, Matthew C Baker, et al.
Acta Neuropathologica|August 8, 2013
Progressive amnestic dementia, hippocampal sclerosis, and mutation in C9ORF72Melissa E Murray, Kevin F Bieniek, M Banks Greenberg, et al.
Cell Reports|April 9, 2025
Differential neuronal vulnerability to C9orf72 repeat expansion driven by Xbp1-induced endoplasmic reticulum-associated degradationDunxin Shen, Alec Vincent, Evan Udine, et al.
Human Molecular Genetics|May 31, 2012
Evidence for an oligogenic basis of amyotrophic lateral sclerosisMarka van Blitterswijk, Michael A van Es, Eric A M Hennekam, et al.
Annals of Neurology|June 29, 2010
Paraoxonase gene mutations in amyotrophic lateral sclerosisNicola Ticozzi, Ashley Lyn LeClerc, Pamela J Keagle, et al.
Pageof 9

Showing results (31-40 of 89) with videos related to

Sort By:
Pageof 9
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 3, 2013
Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementiaMarka van Blitterswijk, Matthew C Baker, Kevin F Bieniek, et al.
Neurobiology of Aging|February 15, 2012
Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patientsMarka van Blitterswijk, Anna Blokhuis, Michael A van Es, et al.
Brain Pathology (Zurich, Switzerland)|July 11, 2024
Upper motor neuron-predominant motor neuron disease presenting as atypical parkinsonism: A clinicopathological studyAya Murakami, Shunsuke Koga, Shinsuke Fujioka, et al.
Biorxiv : the Preprint Server for Biology|July 16, 2025
Expanding the spectrum of annexin A11 proteinopathy in frontotemporal lobar degeneration and motor neuron diseaseNikhil B Ghayal, Richard J Crook, Angita Jain, et al.
Plos One|November 17, 2012
Genetic overlap between apparently sporadic motor neuron diseasesMarka van Blitterswijk, Lotte Vlam, Michael A van Es, et al.
Molecular Neurodegeneration|February 1, 2020
Elevated methylation levels, reduced expression levels, and frequent contractions in a clinical cohort of C9orf72 expansion carriersJazmyne L Jackson, NiCole A Finch, Matthew C Baker, et al.
Acta Neuropathologica|August 8, 2013
Progressive amnestic dementia, hippocampal sclerosis, and mutation in C9ORF72Melissa E Murray, Kevin F Bieniek, M Banks Greenberg, et al.
Cell Reports|April 9, 2025
Differential neuronal vulnerability to C9orf72 repeat expansion driven by Xbp1-induced endoplasmic reticulum-associated degradationDunxin Shen, Alec Vincent, Evan Udine, et al.
Human Molecular Genetics|May 31, 2012
Evidence for an oligogenic basis of amyotrophic lateral sclerosisMarka van Blitterswijk, Michael A van Es, Eric A M Hennekam, et al.
Annals of Neurology|June 29, 2010
Paraoxonase gene mutations in amyotrophic lateral sclerosisNicola Ticozzi, Ashley Lyn LeClerc, Pamela J Keagle, et al.
Pageof 9