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American Journal of Human Genetics
|
May 26, 2015
Jump from pre-mutation to pathologic expansion in C9orf72
Zhengrui Xi, Marka van Blitterswijk, Ming Zhang, et al.
Brain Pathology (Zurich, Switzerland)
|
March 12, 2021
Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficits
Rosa Rademakers, Alexandra M Nicholson, Yingxue Ren, et al.
The Lancet. Neurology
|
September 10, 2013
Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study
Marka van Blitterswijk, Mariely DeJesus-Hernandez, Ellis Niemantsverdriet, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 9, 2012
Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion
Baber K Khan, Jennifer S Yokoyama, Leonel T Takada, et al.
Science Translational Medicine
|
November 12, 2025
Epstein-Barr virus reprograms autoreactive B cells as antigen-presenting cells in systemic lupus erythematosus
Shady Younis, Salvinaz I Moutusy, Sajede Rasouli, et al.
Annals of Neurology
|
December 4, 2020
Lewy Body Disease is a Contributor to Logopenic Progressive Aphasia Phenotype
Marina Buciuc, Jennifer L Whitwell, Koji Kasanuki, et al.
Acta Neuropathologica Communications
|
October 10, 2019
Extensive transcriptomic study emphasizes importance of vesicular transport in C9orf72 expansion carriers
Dennis W Dickson, Matthew C Baker, Jazmyne L Jackson, et al.
Brain : a Journal of Neurology
|
April 23, 2021
Long-read targeted sequencing uncovers clinicopathological associations for C9orf72-linked diseases
Mariely DeJesus-Hernandez, Ross A Aleff, Jazmyne L Jackson, et al.
Acta Neuropathologica
|
October 7, 2015
Novel clinical associations with specific C9ORF72 transcripts in patients with repeat expansions in C9ORF72
Marka van Blitterswijk, Tania F Gendron, Matthew C Baker, et al.
Translational Neurodegeneration
|
October 29, 2025
Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases
Gang Wu, Wenan Chen, Joanne Wuu, et al.
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of 13
Search research articles
Search
Showing results (101-110 of 122) with videos related to
Sort By:
Page
of 13
American Journal of Human Genetics
|
May 26, 2015
Jump from pre-mutation to pathologic expansion in C9orf72
Zhengrui Xi, Marka van Blitterswijk, Ming Zhang, et al.
Brain Pathology (Zurich, Switzerland)
|
March 12, 2021
Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficits
Rosa Rademakers, Alexandra M Nicholson, Yingxue Ren, et al.
The Lancet. Neurology
|
September 10, 2013
Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study
Marka van Blitterswijk, Mariely DeJesus-Hernandez, Ellis Niemantsverdriet, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 9, 2012
Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion
Baber K Khan, Jennifer S Yokoyama, Leonel T Takada, et al.
Science Translational Medicine
|
November 12, 2025
Epstein-Barr virus reprograms autoreactive B cells as antigen-presenting cells in systemic lupus erythematosus
Shady Younis, Salvinaz I Moutusy, Sajede Rasouli, et al.
Annals of Neurology
|
December 4, 2020
Lewy Body Disease is a Contributor to Logopenic Progressive Aphasia Phenotype
Marina Buciuc, Jennifer L Whitwell, Koji Kasanuki, et al.
Acta Neuropathologica Communications
|
October 10, 2019
Extensive transcriptomic study emphasizes importance of vesicular transport in C9orf72 expansion carriers
Dennis W Dickson, Matthew C Baker, Jazmyne L Jackson, et al.
Brain : a Journal of Neurology
|
April 23, 2021
Long-read targeted sequencing uncovers clinicopathological associations for C9orf72-linked diseases
Mariely DeJesus-Hernandez, Ross A Aleff, Jazmyne L Jackson, et al.
Acta Neuropathologica
|
October 7, 2015
Novel clinical associations with specific C9ORF72 transcripts in patients with repeat expansions in C9ORF72
Marka van Blitterswijk, Tania F Gendron, Matthew C Baker, et al.
Translational Neurodegeneration
|
October 29, 2025
Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases
Gang Wu, Wenan Chen, Joanne Wuu, et al.
Page
of 13