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[HTML][HTML] Translating state-of-the-art spinal cord MRI techniques to clinical use: A systematic review of clinical studies utilizing DTI, MT, MWF, MRS, and fMRI
Background A recent meeting of international imaging experts sponsored by the
International Spinal Research Trust (ISRT) and the Wings for Life Foundation identified 5 …
International Spinal Research Trust (ISRT) and the Wings for Life Foundation identified 5 …
From animal models to human disease: a genetic approach for personalized medicine in ALS
Abstract Amyotrophic Lateral Sclerosis (ALS) is the most frequent motor neuron disease in
adults. Classical ALS is characterized by the death of upper and lower motor neurons …
adults. Classical ALS is characterized by the death of upper and lower motor neurons …
SCT: Spinal Cord Toolbox, an open-source software for processing spinal cord MRI data
For the past 25 years, the field of neuroimaging has witnessed the development of several
software packages for processing multi-parametric magnetic resonance imaging (mpMRI) to …
software packages for processing multi-parametric magnetic resonance imaging (mpMRI) to …
Pain in amyotrophic lateral sclerosis
Pain is a largely neglected symptom in patients with amyotrophic lateral sclerosis (ALS)
although it is reported by most of these patients. It occurs at all stages of the disease and can …
although it is reported by most of these patients. It occurs at all stages of the disease and can …
Identification of GGC repeat expansion in the NOTCH2NLC gene in amyotrophic lateral sclerosis
Y Yuan, Z Liu, X Hou, W Li, J Ni, L Huang, Y Hu, P Liu… - Neurology, 2020 - neurology.org
Objective To determine whether the GGC repeats in the NOTCH2NLC gene contribute to
amyotrophic lateral sclerosis (ALS). Methods In this study, 545 patients with ALS and 1,305 …
amyotrophic lateral sclerosis (ALS). Methods In this study, 545 patients with ALS and 1,305 …
Diagnostics of amyotrophic lateral sclerosis: up to date
I Štětkářová, E Ehler - Diagnostics, 2021 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease
characterized by gradual loss of upper and lower motor neurons and their pathways, usually …
characterized by gradual loss of upper and lower motor neurons and their pathways, usually …
Spinal cord imaging in amyotrophic lateral sclerosis: historical concepts—novel techniques
Amyotrophic lateral sclerosis (ALS) is the most common adult onset motor neuron disease
with no effective disease modifying therapies at present. Spinal cord degeneration is a …
with no effective disease modifying therapies at present. Spinal cord degeneration is a …
Amyotrophic lateral sclerosis: Current perspectives from basic research to the clinic
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by
progressive degeneration of upper and lower motoneurons, leading to muscle weakness …
progressive degeneration of upper and lower motoneurons, leading to muscle weakness …
Non-motor symptoms in patients with amyotrophic lateral sclerosis: current state and future directions
B Bjelica, MB Bartels, J Hesebeck-Brinckmann… - Journal of …, 2024 - Springer
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by
the progressive degeneration of both upper and lower motor neurons. A defining …
the progressive degeneration of both upper and lower motor neurons. A defining …
“Switchboard” malfunction in motor neuron diseases: Selective pathology of thalamic nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis
The thalamus is a key cerebral hub relaying a multitude of corticoefferent and corticoafferent
connections and mediating distinct extrapyramidal, sensory, cognitive and behavioural …
connections and mediating distinct extrapyramidal, sensory, cognitive and behavioural …