The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.
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Characterization of the properties of a novel mutation in VAPB in familial amyotrophic lateral sclerosisUbiquilin-2 (UBQLN2) binds with high affinity to the C-terminal region of TDP-43 and modulates TDP-43 levels in H4 cells: characterization of inhibition by nucleic acids and 4-aminoquinolinesMolecular motor proteins and amyotrophic lateral sclerosisFrontotemporal dementia: a bridge between dementia and neuromuscular diseasePlatelet serotonin level predicts survival in amyotrophic lateral sclerosisWhat causes amyotrophic lateral sclerosis?Sleep disorders in neurodegenerative diseases.Development of a novel nonradiometric assay for nucleic acid binding to TDP-43 suitable for high-throughput screening using AlphaScreen technology.Angiogenin levels and ANG genotypes: dysregulation in amyotrophic lateral sclerosisNeuroprotective effects of lithium: implications for the treatment of Alzheimer's disease and related neurodegenerative disordersAmyotrophic lateral sclerosis and frontotemporal lobar degeneration: a spectrum of TDP-43 proteinopathies.Altered patterns of cortical activation in ALS patients during attention and cognitive response inhibition tasks.On the development of markers for pathological TDP-43 in amyotrophic lateral sclerosis with and without dementia.Role of the Insulin-Like Growth Factor Type 1 Receptor in the Pathogenesis of Diabetic Encephalopathy.Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutationsCharacterization of a series of 4-aminoquinolines that stimulate caspase-7 mediated cleavage of TDP-43 and inhibit its function.Engaging in patient decision-making in multidisciplinary care for amyotrophic lateral sclerosis: the views of health professionalsAutophagy and neuronal cell death in neurological disordersCorticospinal motor neurons and related subcerebral projection neurons undergo early and specific neurodegeneration in hSOD1G⁹³A transgenic ALS mice.Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriers.FTD and ALS: a tale of two diseasesAmyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases.The role of RNA processing in the pathogenesis of motor neuron degeneration.Emerging drugs for amyotrophic lateral sclerosis.The frontotemporal syndromes of ALS. Clinicopathological correlates.TDP-43 and FUS/TLS: sending a complex message about messenger RNA in amyotrophic lateral sclerosis?TARDBP and FUS mutations associated with amyotrophic lateral sclerosis: summary and update.Amyotrophic lateral sclerosis: applications of stem cells - an update.Challenges in the Understanding and Treatment of Amyotrophic Lateral Sclerosis/Motor Neuron Disease.Molecular basis of ALS and FTD: implications for translational studies.Postulated vasoactive neuropeptide immunopathology affecting the blood-brain/blood-spinal barrier in certain neuropsychiatric fatigue-related conditions: A role for phosphodiesterase inhibitors in treatment?Widespread structural brain involvement in ALS is not limited to the C9orf72 repeat expansion.Widespread neuronal and glial hyperphosphorylated tau deposition in ALS with cognitive impairment.Opportunity and innovation in studying pre-symptomatic amyotrophic lateral sclerosis.Amyotrophic lateral sclerosis - frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria.Neuroanatomical correlates of apathy in ALS using 4 Tesla diffusion tensor MRI.Insight in ALS: awareness of behavioral change in patients with and without FTD.White matter structural network abnormalities underlie executive dysfunction in amyotrophic lateral sclerosis.Lipid Metabolism and Survival Across the Frontotemporal Dementia-Amyotrophic Lateral Sclerosis Spectrum: Relationships to Eating Behavior and Cognition.BNCI systems as a potential assistive technology: ethical issues and participatory research in the BrainAble project.
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The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on December 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
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name
The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.
@en
The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.
@nl
type
label
The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.
@en
The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.
@nl
prefLabel
The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.
@en
The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.
@nl
P2860
P1476
The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis
@en
P2093
Michael J Strong
P2860
P304
P356
10.1080/17482960802372371
P577
2008-12-01T00:00:00Z