Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis. - Wikidata - awgldk - TriplyDB

Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis.

Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis.

http://www.wikidata.org/entity/Q51868850

about

Widespread structural and functional connectivity changes in amyotrophic lateral sclerosis: insights from advanced neuroimaging research Clinical and genetic basis of familial amyotrophic lateral sclerosis Modeling ALS and FTD with iPSC-derived neurons The function of RNA-binding proteins at the synapse: implications for neurodegeneration Frontotemporal dementia: a bridge between dementia and neuromuscular disease Profiling Speech and Pausing in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD)What influences patient decision-making in amyotrophic lateral sclerosis multidisciplinary care? A study of patient perspectives.Cognitive-behavioral screening reveals prevalent impairment in a large multicenter ALS cohort.The verbal fluency index: Dutch normative data for cognitive testing in ALS.Syntactic comprehension in patients with amyotrophic lateral sclerosis.The Mental Status Examination in Patients With Suspected Dementia.Adiponectin levels in the serum and cerebrospinal fluid of amyotrophic lateral sclerosis patients: possible influence on neuroinflammation?Structural explanation of poor prognosis of amyotrophic lateral sclerosis in the non-demented state Action verb comprehension in amyotrophic lateral sclerosis and Parkinson's disease.Survival profiles of patients with frontotemporal dementia and motor neuron disease.TAR DNA-binding protein 43 in neurodegenerative disease.Frontotemporal dementia and its subtypes: a genome-wide association study.Atypical Alzheimer's disease in an elderly United States resident with amyotrophic lateral sclerosis and pathological tau in spinal motor neurons.Structural and functional hallmarks of amyotrophic lateral sclerosis progression in motor- and memory-related brain regions.Impaired corticopontocerebellar tracts underlie pseudobulbar affect in motor neuron disorders.Narrative discourse deficits in amyotrophic lateral sclerosis ALS-Plus syndrome: non-pyramidal features in a large ALS cohort.Prospective memory tasks: a more sensitive method for screening cognitive impairment in ALS?The cognitive profile of ALS: a systematic review and meta-analysis update.Behavior matters--cognitive predictors of survival in amyotrophic lateral sclerosis.Microstructural white matter changes underlying cognitive and behavioural impairment in ALS--an in vivo study using DTI Hypermethylation of repeat expanded C9orf72 is a clinical and molecular disease modifier.Risk genotypes at TMEM106B are associated with cognitive impairment in amyotrophic lateral sclerosis.Extramotor damage is associated with cognition in primary lateral sclerosis patients Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: a spectrum of TDP-43 proteinopathies.Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine.Deficits in sentence expression in amyotrophic lateral sclerosis.Impaired cognitive flexibility in amyotrophic lateral sclerosis.CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients.Action processing and mirror neuron function in patients with amyotrophic lateral sclerosis: an fMRI study.C9orf72 promoter hypermethylation is neuroprotective: Neuroimaging and neuropathologic evidence.On the development of markers for pathological TDP-43 in amyotrophic lateral sclerosis with and without dementia.Neuropsychological investigation in Chinese patients with progressive muscular atrophy Cognitive Impairment in Chinese Patients with Sporadic Amyotrophic Lateral Sclerosis.Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

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Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis.

http://www.wikidata.org/entity/Q51868850

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2009年学术文章

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Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

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Christen Shoesmith

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Denise Figlewicz

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P Nigel Leigh

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Susan Woolley

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P2860

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)

A rating scale for depression

An Inventory for Measuring Depression

The hospital anxiety and depression scale

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

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

Familial non-specific dementia maps to chromosome 3

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

CHMP2B mutations are not a common cause of frontotemporal lobar degeneration

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

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Laura H. Goldstein

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