Search research articles
Contact Us
Filters
Showing results (21-30 of 56) with videos related to
Page
of 6
Sort By:
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
May 10, 2024
Short tandem repeat expansions in <i>LRP12</i> are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry
Lyndal Henden, Liam G Fearnley, Dean Southwood, et al.
Archives of Neurology
|
April 23, 2003
Identifying the pattern of olfactory deficits in Parkinson disease using the brief smell identification test
Kay L Double, Dominic B Rowe, Michael Hayes, et al.
Molecular Neurodegeneration
|
April 24, 2025
Multi-region brain transcriptomic analysis of amyotrophic lateral sclerosis reveals widespread RNA alterations and substantial cerebellum involvement
Natalie Grima, Andrew N Smith, Claire E Shepherd, et al.
Brain : a Journal of Neurology
|
December 21, 2022
Riluzole is associated with decreasing neuritic plaque severity in amyotrophic lateral sclerosis
Srestha Mazumder, Heather McCann, Susan D'Silva, et al.
Neurobiology of Aging
|
September 10, 2015
Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese origin
Kelly L Williams, Emily P McCann, Jennifer A Fifita, et al.
NPJ Genomic Medicine
|
August 14, 2020
Identity by descent analysis identifies founder events and links <i>SOD1</i> familial and sporadic ALS cases
Lyndal Henden, Natalie A Twine, Piotr Szul, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 28, 2012
The phenotypic spectrum of dystonia in Mohr-Tranebjaerg syndrome
Ainhi D Ha, Kaitlyn L Parratt, Nanna D Rendtorff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 19, 2009
Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?
Greg T Sutherland, Glenda M Halliday, Peter A Silburn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 17, 2008
Mitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian community
Prachi Mehta, George D Mellick, Dominic B Rowe, et al.
Acta Neuropathologica Communications
|
November 14, 2023
Heterogeneity of cortical pTDP-43 inclusion morphologies in amyotrophic lateral sclerosis
Rachel H Tan, Heather McCann, Claire E Shepherd, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 56) with videos related to
Sort By:
Page
of 6
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
May 10, 2024
Short tandem repeat expansions in <i>LRP12</i> are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry
Lyndal Henden, Liam G Fearnley, Dean Southwood, et al.
Archives of Neurology
|
April 23, 2003
Identifying the pattern of olfactory deficits in Parkinson disease using the brief smell identification test
Kay L Double, Dominic B Rowe, Michael Hayes, et al.
Molecular Neurodegeneration
|
April 24, 2025
Multi-region brain transcriptomic analysis of amyotrophic lateral sclerosis reveals widespread RNA alterations and substantial cerebellum involvement
Natalie Grima, Andrew N Smith, Claire E Shepherd, et al.
Brain : a Journal of Neurology
|
December 21, 2022
Riluzole is associated with decreasing neuritic plaque severity in amyotrophic lateral sclerosis
Srestha Mazumder, Heather McCann, Susan D'Silva, et al.
Neurobiology of Aging
|
September 10, 2015
Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese origin
Kelly L Williams, Emily P McCann, Jennifer A Fifita, et al.
NPJ Genomic Medicine
|
August 14, 2020
Identity by descent analysis identifies founder events and links <i>SOD1</i> familial and sporadic ALS cases
Lyndal Henden, Natalie A Twine, Piotr Szul, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 28, 2012
The phenotypic spectrum of dystonia in Mohr-Tranebjaerg syndrome
Ainhi D Ha, Kaitlyn L Parratt, Nanna D Rendtorff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 19, 2009
Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?
Greg T Sutherland, Glenda M Halliday, Peter A Silburn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 17, 2008
Mitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian community
Prachi Mehta, George D Mellick, Dominic B Rowe, et al.
Acta Neuropathologica Communications
|
November 14, 2023
Heterogeneity of cortical pTDP-43 inclusion morphologies in amyotrophic lateral sclerosis
Rachel H Tan, Heather McCann, Claire E Shepherd, et al.
Page
of 6