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Neurofilament proteins as biomarkers to monitor neurological diseases and the efficacy of therapies
Biomarkers of neurodegeneration and neuronal injury have the potential to improve
diagnostic accuracy, disease monitoring, prognosis, and measure treatment efficacy …
diagnostic accuracy, disease monitoring, prognosis, and measure treatment efficacy …
Blood neurofilament light: a critical review of its application to neurologic disease
Neuronal injury is a universal event that occurs in disease processes that affect both the
central and peripheral nervous systems. A blood biomarker linked to neuronal injury would …
central and peripheral nervous systems. A blood biomarker linked to neuronal injury would …
Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis
F Verde, P Steinacker, JH Weishaupt… - Journal of Neurology …, 2019 - jnnp.bmj.com
Objective To determine the diagnostic and prognostic performance of serum neurofilament
light chain (NFL) in amyotrophic lateral sclerosis (ALS). Methods This single-centre …
light chain (NFL) in amyotrophic lateral sclerosis (ALS). Methods This single-centre …
RNA dysregulation in amyotrophic lateral sclerosis
Z Butti, SA Patten - Frontiers in genetics, 2019 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is the most common adult-onset motor neuron disease
and is characterized by the degeneration of upper and lower motor neurons. It has become …
and is characterized by the degeneration of upper and lower motor neurons. It has become …
ALS: a disease of motor neurons and their nonneuronal neighbors
S Boillée, CV Velde, DW Cleveland - Neuron, 2006 - cell.com
Amyotrophic lateral sclerosis is a late-onset progressive neurodegenerative disease
affecting motor neurons. The etiology of most ALS cases remains unknown, but 2% of …
affecting motor neurons. The etiology of most ALS cases remains unknown, but 2% of …
Oxidative stress in ALS: key role in motor neuron injury and therapeutic target
SC Barber, PJ Shaw - Free Radical Biology and Medicine, 2010 - Elsevier
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disorder
characterized by death of motor neurons leading to muscle wasting, paralysis, and death …
characterized by death of motor neurons leading to muscle wasting, paralysis, and death …
Cytoplasmic mislocalization of TDP-43 is toxic to neurons and enhanced by a mutation associated with familial amyotrophic lateral sclerosis
Mutations in the gene encoding TDP-43—the major protein component of neuronal
aggregates characteristic of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar …
aggregates characteristic of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar …
ALS pathogenesis and therapeutic approaches: the role of mesenchymal stem cells and extracellular vesicles
R Bonafede, R Mariotti - Frontiers in cellular neuroscience, 2017 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by
progressive muscle paralysis determined by the degeneration of motoneurons in the motor …
progressive muscle paralysis determined by the degeneration of motoneurons in the motor …
Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis
MJ Strong, GM Grace, M Freedman… - Amyotrophic Lateral …, 2009 - Taylor & Francis
Amyotrophic lateral sclerosis (ALS) is increasingly recognized to be a multisystem disorder
which includes both clinical and neuropathological features of a frontotemporal lobar …
which includes both clinical and neuropathological features of a frontotemporal lobar …
Diagnostic and prognostic performance of neurofilaments in ALS
K Poesen, P Van Damme - Frontiers in neurology, 2019 - frontiersin.org
There is a need for biomarkers for amyotrophic lateral sclerosis (ALS), to support the
diagnosis of the disease, to predict disease progression and to track disease activity and …
diagnosis of the disease, to predict disease progression and to track disease activity and …