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Annals of Clinical and Translational Neurology
|
December 15, 2023
Reduced Bergmann glial process terminations and lateral appendages in essential tremor
David S Ruff, Ilaria Balbo, Ruo-Yah Lai, et al.
Acta Neuropathologica
|
January 6, 2023
Histopathology of the cerebellar cortex in essential tremor and other neurodegenerative motor disorders: comparative analysis of 320 brains
Elan D Louis, Regina T Martuscello, John T Gionco, et al.
Cerebellum (London, England)
|
April 2, 2017
Cerebellar Pathology in Familial vs. Sporadic Essential Tremor
Elan D Louis, Sheng-Han Kuo, Jie Wang, et al.
Cerebellum (London, England)
|
October 12, 2016
Cerebellar Pathology in Early Onset and Late Onset Essential Tremor
Sheng-Han Kuo, Jie Wang, William J Tate, et al.
The Journal of Clinical Investigation
|
March 5, 2026
A therapeutic role for a regulatory glucose transporter1 (GLUT1)-associated lncRNA in GLUT1-deficient mice
Maoxue Tang, Sasa Teng, Yueqing Peng, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 16, 2009
Older onset essential tremor: More rapid progression and more degenerative pathology
Elan D Louis, Phyllis L Faust, Jean-Paul G Vonsattel, et al.
Acta Neuropathologica
|
July 19, 2019
Contextualizing the pathology in the essential tremor cerebellar cortex: a patholog-omics approach
Elan D Louis, Chloë A Kerridge, Debotri Chatterjee, et al.
Acta Neuropathologica
|
October 6, 2016
Climbing fiber-Purkinje cell synaptic pathology in tremor and cerebellar degenerative diseases
Sheng-Han Kuo, Chi-Ying Lin, Jie Wang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 23, 2023
Patterns of TDP-43 Deposition in Brains with LRRK2 G2019S Mutations
Julian Agin-Liebes, Richard A Hickman, Jean Paul Vonsattel, et al.
European Journal of Medical Genetics
|
September 5, 2016
Whole exome sequencing identifies a homozygous POLG2 missense variant in an infant with fulminant hepatic failure and mitochondrial DNA depletion
Hemant Varma, Phyllis L Faust, Alejandro D Iglesias, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 104) with videos related to
Sort By:
Page
of 11
Annals of Clinical and Translational Neurology
|
December 15, 2023
Reduced Bergmann glial process terminations and lateral appendages in essential tremor
David S Ruff, Ilaria Balbo, Ruo-Yah Lai, et al.
Acta Neuropathologica
|
January 6, 2023
Histopathology of the cerebellar cortex in essential tremor and other neurodegenerative motor disorders: comparative analysis of 320 brains
Elan D Louis, Regina T Martuscello, John T Gionco, et al.
Cerebellum (London, England)
|
April 2, 2017
Cerebellar Pathology in Familial vs. Sporadic Essential Tremor
Elan D Louis, Sheng-Han Kuo, Jie Wang, et al.
Cerebellum (London, England)
|
October 12, 2016
Cerebellar Pathology in Early Onset and Late Onset Essential Tremor
Sheng-Han Kuo, Jie Wang, William J Tate, et al.
The Journal of Clinical Investigation
|
March 5, 2026
A therapeutic role for a regulatory glucose transporter1 (GLUT1)-associated lncRNA in GLUT1-deficient mice
Maoxue Tang, Sasa Teng, Yueqing Peng, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 16, 2009
Older onset essential tremor: More rapid progression and more degenerative pathology
Elan D Louis, Phyllis L Faust, Jean-Paul G Vonsattel, et al.
Acta Neuropathologica
|
July 19, 2019
Contextualizing the pathology in the essential tremor cerebellar cortex: a patholog-omics approach
Elan D Louis, Chloë A Kerridge, Debotri Chatterjee, et al.
Acta Neuropathologica
|
October 6, 2016
Climbing fiber-Purkinje cell synaptic pathology in tremor and cerebellar degenerative diseases
Sheng-Han Kuo, Chi-Ying Lin, Jie Wang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 23, 2023
Patterns of TDP-43 Deposition in Brains with LRRK2 G2019S Mutations
Julian Agin-Liebes, Richard A Hickman, Jean Paul Vonsattel, et al.
European Journal of Medical Genetics
|
September 5, 2016
Whole exome sequencing identifies a homozygous POLG2 missense variant in an infant with fulminant hepatic failure and mitochondrial DNA depletion
Hemant Varma, Phyllis L Faust, Alejandro D Iglesias, et al.
Page
of 11