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Marka van Blitterswijk

Showing results (11-20 of 89) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|January 16, 2021
Unravelling the clinical spectrum and the role of repeat length in <i>C9ORF72</i> repeat expansionsEmma L van der Ende, Jazmyne L Jackson, Adrianna White, et al.
The Lancet. Neurology|February 22, 2025
Amyotrophic lateral sclerosis caused by hexanucleotide repeat expansions in C9orf72: from genetics to therapeuticsSarah Mizielinska, Guillaume M Hautbergue, Tania F Gendron, et al.
Med (New York, N.Y.)|October 14, 2025
The role of mitochondrial genetics in Parkinson's disease: Long-read sequencing as an emerging methodNgan Le Kim Tran, Marka van Blitterswijk, Wolfdieter Springer, et al.
European Neurology|May 28, 2014
ALS-FTD complex disorder due to C9ORF72 gene mutation: description of first Polish familyJoanna Siuda, Tatiana Lewicka, Malgorzata Bujak, et al.
Neurology|September 12, 2014
Identical twins with the C9orf72 repeat expansion are discordant for ALSZhengrui Xi, Yana Yunusova, Marka van Blitterswijk, et al.
Neurobiology of Aging|December 25, 2009
Mutational analysis of TARDBP in neurodegenerative diseasesNicola Ticozzi, Ashley Lyn LeClerc, Marka van Blitterswijk, et al.
Neurobiology of Aging|October 16, 2012
Mutational analysis of TARDBP in Parkinson's diseaseMarka van Blitterswijk, Michael A van Es, Dagmar Verbaan, et al.
Molecular Neurodegeneration|July 5, 2018
TMEM106B haplotypes have distinct gene expression patterns in aged brainYingxue Ren, Marka van Blitterswijk, Mariet Allen, et al.
Annals of Clinical and Translational Neurology|August 27, 2019
Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutationsNobutaka Sakae, Shanu F Roemer, Kevin F Bieniek, et al.
Plos One|April 12, 2013
Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-SeqMarka van Blitterswijk, Eric T Wang, Brad A Friedman, et al.
Pageof 9

Showing results (11-20 of 89) with videos related to

Sort By:
Pageof 9
Journal of Neurology, Neurosurgery, and Psychiatry|January 16, 2021
Unravelling the clinical spectrum and the role of repeat length in <i>C9ORF72</i> repeat expansionsEmma L van der Ende, Jazmyne L Jackson, Adrianna White, et al.
The Lancet. Neurology|February 22, 2025
Amyotrophic lateral sclerosis caused by hexanucleotide repeat expansions in C9orf72: from genetics to therapeuticsSarah Mizielinska, Guillaume M Hautbergue, Tania F Gendron, et al.
Med (New York, N.Y.)|October 14, 2025
The role of mitochondrial genetics in Parkinson's disease: Long-read sequencing as an emerging methodNgan Le Kim Tran, Marka van Blitterswijk, Wolfdieter Springer, et al.
European Neurology|May 28, 2014
ALS-FTD complex disorder due to C9ORF72 gene mutation: description of first Polish familyJoanna Siuda, Tatiana Lewicka, Malgorzata Bujak, et al.
Neurology|September 12, 2014
Identical twins with the C9orf72 repeat expansion are discordant for ALSZhengrui Xi, Yana Yunusova, Marka van Blitterswijk, et al.
Neurobiology of Aging|December 25, 2009
Mutational analysis of TARDBP in neurodegenerative diseasesNicola Ticozzi, Ashley Lyn LeClerc, Marka van Blitterswijk, et al.
Neurobiology of Aging|October 16, 2012
Mutational analysis of TARDBP in Parkinson's diseaseMarka van Blitterswijk, Michael A van Es, Dagmar Verbaan, et al.
Molecular Neurodegeneration|July 5, 2018
TMEM106B haplotypes have distinct gene expression patterns in aged brainYingxue Ren, Marka van Blitterswijk, Mariet Allen, et al.
Annals of Clinical and Translational Neurology|August 27, 2019
Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutationsNobutaka Sakae, Shanu F Roemer, Kevin F Bieniek, et al.
Plos One|April 12, 2013
Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-SeqMarka van Blitterswijk, Eric T Wang, Brad A Friedman, et al.
Pageof 9