The changing scene of amyotrophic lateral sclerosis
W Robberecht, T Philips - Nature Reviews Neuroscience, 2013 - nature.com
Several recent breakthroughs have provided notable insights into the pathogenesis of
amyotrophic lateral sclerosis (ALS), with some even shifting our thinking about this …
amyotrophic lateral sclerosis (ALS), with some even shifting our thinking about this …
Deciphering amyotrophic lateral sclerosis: what phenotype, neuropathology and genetics are telling us about pathogenesis
Amyotrophic lateral sclerosis (ALS) is characterized phenotypically by progressive
weakness and neuropathologically by loss of motor neurons. Phenotypically, there is …
weakness and neuropathologically by loss of motor neurons. Phenotypically, there is …
Amyotrophic lateral sclerosis: mechanisms and therapeutics in the epigenomic era
X Paez-Colasante, C Figueroa-Romero… - Nature Reviews …, 2015 - nature.com
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease of the motor
neurons, which results in weakness and atrophy of voluntary skeletal muscles. Treatments …
neurons, which results in weakness and atrophy of voluntary skeletal muscles. Treatments …
The pathobiology of amyotrophic lateral sclerosis: a proteinopathy?
MJ Strong, S Kesavapany… - Journal of Neuropathology …, 2005 - academic.oup.com
Amyotrophic lateral sclerosis (ALS) is increasingly considered to be a disorder of multiple
etiologies that have in common progressive degeneration of both upper and lower motor …
etiologies that have in common progressive degeneration of both upper and lower motor …
The neurobiology of amyotrophic lateral sclerosis
A Bento‐Abreu, P Van Damme… - European Journal of …, 2010 - Wiley Online Library
Amyotrophic lateral sclerosis is a degenerative disease affecting the motor neurons. In spite
of our growing insights into its biology, it remains a lethal condition. The identification of the …
of our growing insights into its biology, it remains a lethal condition. The identification of the …
ALS: astrocytes move in as deadly neighbors
JP Julien - Nature neuroscience, 2007 - nature.com
Amyotrophic lateral sclerosis (ALS) is characterized by the selective degeneration of motor
neurons. Two independent studies in this issue show that astrocytes expressing a mutation …
neurons. Two independent studies in this issue show that astrocytes expressing a mutation …
Amyotrophic lateral sclerosis: a neurodegenerative disorder poised for successful therapeutic translation
Amyotrophic lateral sclerosis (ALS) is a devastating disease caused by degeneration of
motor neurons. As with all major neurodegenerative disorders, development of disease …
motor neurons. As with all major neurodegenerative disorders, development of disease …
Emerging mechanisms of molecular pathology in ALS
Amyotrophic lateral sclerosis (ALS) is a devastating degenerative disease characterized by
progressive loss of motor neurons in the motor cortex, brainstem, and spinal cord. Although …
progressive loss of motor neurons in the motor cortex, brainstem, and spinal cord. Although …
Common molecular pathways in amyotrophic lateral sclerosis and frontotemporal dementia
JH Weishaupt, T Hyman, I Dikic - Trends in molecular medicine, 2016 - cell.com
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are age-related
neurodegenerative diseases in which predominantly motor neurons and cerebral cortex …
neurodegenerative diseases in which predominantly motor neurons and cerebral cortex …
Non-cell-autonomous pathogenic mechanisms in amyotrophic lateral sclerosis
ACM Van Harten, H Phatnani, S Przedborski - Trends in neurosciences, 2021 - cell.com
Amyotrophic lateral sclerosis (ALS) is the most common adult-onset paralytic disorder,
characterized mainly by a loss of motor neurons (MNs) in the CNS. Over the past decades …
characterized mainly by a loss of motor neurons (MNs) in the CNS. Over the past decades …