Grey and white matter changes across the amyotrophic lateral sclerosis-frontotemporal dementia continuum. - Wikidata - awgldk - TriplyDB

Grey and white matter changes across the amyotrophic lateral sclerosis-frontotemporal dementia continuum.

Grey and white matter changes across the amyotrophic lateral sclerosis-frontotemporal dementia continuum.

http://www.wikidata.org/entity/Q34406028

about

What does imaging reveal about the pathology of amyotrophic lateral sclerosis?Brain connectivity in neurodegenerative diseases--from phenotype to proteinopathy.Propagation of pathology through brain networks in neurodegenerative diseases: from molecules to clinical phenotypes.Survival prediction in Amyotrophic lateral sclerosis based on MRI measures and clinical characteristics Side of limb-onset predicts laterality of gray matter loss in amyotrophic lateral sclerosis.Cerebellar integrity in the amyotrophic lateral sclerosis-frontotemporal dementia continuum Narrative discourse deficits in amyotrophic lateral sclerosis Relating brain anatomy and cognitive ability using a multivariate multimodal framework The cognitive profile of ALS: a systematic review and meta-analysis update.Neuroimaging in frontotemporal dementia.Mapping cortical degeneration in ALS with magnetization transfer ratio and voxel-based morphometry.Shape analysis of the corpus callosum in Alzheimer's disease and frontotemporal lobar degeneration subtypes White matter disease contributes to apathy and disinhibition in behavioral variant frontotemporal dementia.Longitudinal diffusion tensor imaging in frontotemporal dementia.Longitudinal grey and white matter changes in frontotemporal dementia and Alzheimer's disease Microstructural changes across different clinical milestones of disease in amyotrophic lateral sclerosis.Personality disturbances in amyotrophic lateral sclerosis: a case study demonstrating changes in personality without cognitive deficits.An Assessment of Possible Neuropathology and Clinical Relationships in 46 Sporadic Amyotrophic Lateral Sclerosis Patient Autopsies Microstructural Correlates of Emotional Attribution Impairment in Non-Demented Patients with Amyotrophic Lateral Sclerosis Development of an Automated MRI-Based Diagnostic Protocol for Amyotrophic Lateral Sclerosis Using Disease-Specific Pathognomonic Features: A Quantitative Disease-State Classification Study.Epigallocatechin-3-gallate: a useful, effective and safe clinical approach for targeted prevention and individualised treatment of neurological diseases?Dissociation of Structural and Functional Integrities of the Motor System in Amyotrophic Lateral Sclerosis and Behavioral-Variant Frontotemporal Dementia.Working Memory Network Changes in ALS: An fMRI Study.MRI signatures of brain macrostructural atrophy and microstructural degradation in frontotemporal lobar degeneration subtypes Impaired Perception of Emotional Expression in Amyotrophic Lateral Sclerosis The neural correlates and clinical characteristics of psychosis in the frontotemporal dementia continuum and the C9orf72 expansion.Sequential distribution of pTDP-43 pathology in behavioral variant frontotemporal dementia (bvFTD).Voxel-based mapping of grey matter volume and glucose metabolism profiles in amyotrophic lateral sclerosis.Phenotypic variety in the presentation of frontotemporal lobar degeneration.Beyond and below the cortex: the contribution of striatal dysfunction to cognition and behaviour in neurodegeneration.A longer diagnostic interval is a risk for depression in amyotrophic lateral sclerosis.The Evolution of Caregiver Burden in Frontotemporal Dementia with and without Amyotrophic Lateral Sclerosis.MRI signatures of the frontotemporal lobar degeneration continuum.Motor neuron disease-frontotemporal dementia: a clinical continuum.Semantic deficits in amyotrophic lateral sclerosis.Transcranial Magnetic Stimulation for the Assessment of Neurodegenerative Disease.Voxel-Wise Meta-Analysis of Gray Matter Changes in Amyotrophic Lateral Sclerosis.Cognitive and Behavioral Symptoms in ALSFTD: Detection, Differentiation, and Progression.Examining the language and behavioural profile in FTD and ALS-FTD.Interhemispheric connectivity in amyotrophic lateral sclerosis: A near-infrared spectroscopy and diffusion tensor imaging study.

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Grey and white matter changes across the amyotrophic lateral sclerosis-frontotemporal dementia continuum.

http://www.wikidata.org/entity/Q34406028

description

2012 nî lūn-bûn

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2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2012 թվականի օգոստոսին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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Grey and white matter changes ...... totemporal dementia continuum.

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Grey and white matter changes ...... totemporal dementia continuum.

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Grey and white matter changes ...... totemporal dementia continuum.

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Grey and white matter changes ...... totemporal dementia continuum.

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Grey and white matter changes ...... totemporal dementia continuum.

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Grey and white matter changes ...... totemporal dementia continuum.

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Grey and white matter changes ...... totemporal dementia continuum.

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Grey and white matter changes ...... totemporal dementia continuum.

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Grey and white matter changes ...... totemporal dementia continuum.

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Eneida Mioshi

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James R Burrell

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John R Hodges

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Michael Hornberger

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Patricia Lillo

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Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

Nonparametric permutation tests for functional neuroimaging: a primer with examples

TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease

Fast robust automated brain extraction

Tract-based spatial statistics: voxelwise analysis of multi-subject diffusion data

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Matthew C Kiernan

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amyotrophic lateral sclerosis

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