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Cortical selective vulnerability in motor neuron disease: a morphometric study.

Cortical selective vulnerability in motor neuron disease: a morphometric study.

http://www.wikidata.org/entity/Q44886501

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Widespread structural and functional connectivity changes in amyotrophic lateral sclerosis: insights from advanced neuroimaging research Olesoxime, a cholesterol-like neuroprotectant for the potential treatment of amyotrophic lateral sclerosis ALS Patient Stem Cells for Unveiling Disease Signatures of Motoneuron Susceptibility: Perspectives on the Deadly Mitochondria, ER Stress and Calcium Triad What does imaging reveal about the pathology of amyotrophic lateral sclerosis?Inhibitory synaptic regulation of motoneurons: a new target of disease mechanisms in amyotrophic lateral sclerosis.The involvement of the cerebellum in amyotrophic lateral sclerosis.Evidence of social understanding impairment in patients with amyotrophic lateral sclerosis Magnetization transfer imaging demonstrates a distributed pattern of microstructural changes of the cerebral cortex in amyotrophic lateral sclerosis.Mitochondrial pathobiology in ALS.Structural and functional hallmarks of amyotrophic lateral sclerosis progression in motor- and memory-related brain regions.The cortical signature of amyotrophic lateral sclerosis.Patterns of spontaneous brain activity in amyotrophic lateral sclerosis: a resting-state FMRI study Mitochondrial and Cell Death Mechanisms in Neurodegenerative Diseases.Cerebro-cerebellar connectivity is increased in primary lateral sclerosis.Extent of cortical involvement in amyotrophic lateral sclerosis--an analysis based on cortical thickness The Wobbler mouse model of amyotrophic lateral sclerosis (ALS) displays hippocampal hyperexcitability, and reduced number of interneurons, but no presynaptic vesicle release impairments.Abnormal cortical excitability in sporadic but not homozygous D90A SOD1 ALS Altered patterns of cortical activation in ALS patients during attention and cognitive response inhibition tasks.Diffusion tensor imaging and voxel based morphometry study in amyotrophic lateral sclerosis: relationships with motor disability.Biology of mitochondria in neurodegenerative diseases.Serotonergic mechanisms in amyotrophic lateral sclerosis.Neuroimmunity dynamics and the development of therapeutic strategies for amyotrophic lateral sclerosis.Neonatal neuronal circuitry shows hyperexcitable disturbance in a mouse model of the adult-onset neurodegenerative disease amyotrophic lateral sclerosis Immununochemical Markers of the Amyloid Cascade in the Hippocampus in Motor Neuron Diseases.Cortical synaptic and dendritic spine abnormalities in a presymptomatic TDP-43 model of amyotrophic lateral sclerosis.The mitochondrial permeability transition pore: a molecular target for amyotrophic lateral sclerosis therapy.Altered cortical beta-band oscillations reflect motor system degeneration in amyotrophic lateral sclerosis.Advances in the application of MRI to amyotrophic lateral sclerosis.Amyotrophic lateral sclerosis: a long preclinical period?Inhibitory dysfunction in amyotrophic lateral sclerosis: future therapeutic opportunities.Novel therapies in development that inhibit motor neuron hyperexcitability in amyotrophic lateral sclerosis.Widespread temporo-occipital lobe dysfunction in amyotrophic lateral sclerosis.Integration of structural and functional magnetic resonance imaging in amyotrophic lateral sclerosis.Altered Functionality, Morphology, and Vesicular Glutamate Transporter Expression of Cortical Motor Neurons from a Presymptomatic Mouse Model of Amyotrophic Lateral Sclerosis.Apical dendrite degeneration, a novel cellular pathology for Betz cells in ALS Amyotrophic lateral sclerosis patients show executive impairments on standard neuropsychological measures and an ecologically valid motor-free test of executive functions.Spinal inhibitory interneuron pathology follows motor neuron degeneration independent of glial mutant superoxide dismutase 1 expression in SOD1-ALS mice.Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS).Movement-related cortical potentials in ALS increase at lower and decrease at higher upper motor neuron burden scores.Combined structural and neurochemical evaluation of the corticospinal tract in amyotrophic lateral sclerosis.

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P2860

Cortical selective vulnerability in motor neuron disease: a morphometric study.

http://www.wikidata.org/entity/Q44886501

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2004 nî lūn-bûn

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2004年學術文章

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2004年學術文章

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Cortical selective vulnerability in motor neuron disease: a morphometric study.

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Cortical selective vulnerability in motor neuron disease: a morphometric study.

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Cortical selective vulnerability in motor neuron disease: a morphometric study.

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Cortical selective vulnerability in motor neuron disease: a morphometric study.

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Cortical selective vulnerability in motor neuron disease: a morphometric study.

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Cortical selective vulnerability in motor neuron disease: a morphometric study.

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Kibble M

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Leigh PN

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P2860

From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS

Calbindin D-28k and parvalbumin immunoreactivity in the frontal cortex in patients with frontal lobe dementia of non-Alzheimer type associated with amyotrophic lateral sclerosis.

Cognition, language and behaviour in motor neurone disease: evidence of frontotemporal dysfunction.

Prevalence and correlates of neuropsychological deficits in amyotrophic lateral sclerosis.

Are amyotrophic lateral sclerosis patients cognitively normal?

Frontotemporal dementia with motor neuron disease (amyotrophic lateral sclerosis with dementia).

Two-dimensional versus three-dimensional cell counting: a practical perspective.

Glutamate transporters in neurologic disease.

Calbindin D-28k and parvalbumin in the rat nervous system.

Clinical electrophysiology of the upper and lower motor neuron in amyotrophic lateral sclerosis.

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