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「"Rademakers R "[Author]」の検索結果

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Loss of Tmem106b exacerbates FTLD pathologies and causes motor deficits in progranulin-deficient mice.

Quality of life and caregiver burden in familial frontotemporal lobar degeneration: Analyses of symptomatic and asymptomatic individuals within the LEFFTDS cohort.

GBA variation and susceptibility to multiple system atrophy.

Correction to: Loss of homeostatic microglial phenotype in CSF1R-related Leukoencephalopathy.

Loss of TMEM106B leads to myelination deficits: implications for frontotemporal dementia treatment strategies.

Loss of homeostatic microglial phenotype in CSF1R-related Leukoencephalopathy.

Validation of serum neurofilaments as prognostic and potential pharmacodynamic biomarkers for ALS.

Revised Self-Monitoring Scale: A potential endpoint for frontotemporal dementia clinical trials.

Elevated methylation levels, reduced expression levels, and frequent contractions in a clinical cohort of C9orf72 expansion carriers.

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.

Trajectory of lobar atrophy in asymptomatic and symptomatic GRN mutation carriers: a longitudinal MRI study.

Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint.

Active lifestyles moderate clinical outcomes in autosomal dominant frontotemporal degeneration.

Comparison of sporadic and familial behavioral variant frontotemporal dementia (FTD) in a North American cohort.

Utility of the global CDR plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium.

Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases.

Nonlinear Z-score modeling for improved detection of cognitive abnormality.

Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein.

Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study.

Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration.

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