Pages that link to "Q37678074"
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The following pages link to Sequential distribution of pTDP-43 pathology in behavioral variant frontotemporal dementia (bvFTD). (Q37678074):
Displaying 50 items.
- Neuronal network disintegration: common pathways linking neurodegenerative diseases (Q26750287) (← links)
- Molecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision Medicine (Q26768648) (← links)
- The role of macropinocytosis in the propagation of protein aggregation associated with neurodegenerative diseases (Q26777240) (← links)
- Neurodegenerative diseases: expanding the prion concept (Q27011744) (← links)
- Spreading of pathology in neurodegenerative diseases: a focus on human studies (Q28082279) (← links)
- The use of cerebrospinal fluid and neuropathologic studies in neuropsychiatry practice and research (Q28088291) (← links)
- Beyond words: Pragmatic inference in behavioral variant of frontotemporal degeneration (Q28608578) (← links)
- Propagation of pathology through brain networks in neurodegenerative diseases: from molecules to clinical phenotypes. (Q30962548) (← links)
- Charting Frontotemporal Dementia: From Genes to Networks (Q31029220) (← links)
- Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants (Q33361835) (← links)
- Novel monoclonal antibodies to normal and pathologically altered human TDP-43 proteins (Q33622382) (← links)
- Multiparametric MRI to distinguish early onset Alzheimer's disease and behavioural variant of frontotemporal dementia (Q33763640) (← links)
- Myelin oligodendrocyte basic protein and prognosis in behavioral-variant frontotemporal dementia (Q34079305) (← links)
- ALS-Plus syndrome: non-pyramidal features in a large ALS cohort. (Q34257559) (← links)
- Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine (Q35204586) (← links)
- TDP-43 pathology and neuronal loss in amyotrophic lateral sclerosis spinal cord (Q35260685) (← links)
- Low molecular weight species of TDP-43 generated by abnormal splicing form inclusions in amyotrophic lateral sclerosis and result in motor neuron death. (Q35746425) (← links)
- Incidence and extent of TDP-43 accumulation in aging human brain (Q35759384) (← links)
- Processing ambiguity in a linguistic context: decision-making difficulties in non-aphasic patients with behavioral variant frontotemporal degeneration (Q36210338) (← links)
- SOD1 protein aggregates stimulate macropinocytosis in neurons to facilitate their propagation (Q36234963) (← links)
- Deep clinical and neuropathological phenotyping of Pick disease (Q36586085) (← links)
- Semi-Automated Digital Image Analysis of Pick's Disease and TDP-43 Proteinopathy (Q36737104) (← links)
- Neuropathology of supercentenarians - four autopsy case studies (Q37230835) (← links)
- Functional recovery in new mouse models of ALS/FTLD after clearance of pathological cytoplasmic TDP-43. (Q37451385) (← links)
- Longitudinal imaging in C9orf72 mutation carriers: Relationship to phenotype (Q37497445) (← links)
- Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern Italy. (Q38379891) (← links)
- Typical and atypical pathology in primary progressive aphasia variants (Q38381591) (← links)
- Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype (Q38382217) (← links)
- TDP-43 in amyotrophic lateral sclerosis - is it a prion disease? (Q38407804) (← links)
- MRI signatures of the frontotemporal lobar degeneration continuum. (Q38414131) (← links)
- Prevalence of TDP-43 proteinopathy in cognitively normal older adults: systematic review and meta-analysis. (Q38644831) (← links)
- Amyotrophic lateral sclerosis and frontotemporal dementia: distinct and overlapping changes in eating behaviour and metabolism (Q38715468) (← links)
- Mapping Neurodegenerative Disease Onset and Progression (Q38746445) (← links)
- Protein aggregates stimulate macropinocytosis facilitating their propagation (Q38768323) (← links)
- The frontotemporal dementia-motor neuron disease continuum (Q38778723) (← links)
- Molecular neuropathology of frontotemporal dementia: insights into disease mechanisms from postmortem studies (Q38866202) (← links)
- Longitudinal Memory Profiles in Behavioral-Variant Frontotemporal Dementia and Alzheimer's Disease (Q38906436) (← links)
- Prion-like propagation as a pathogenic principle in frontotemporal dementia. (Q38922025) (← links)
- Amyotrophic lateral sclerosis: moving towards a new classification system (Q38959347) (← links)
- Pathology of Neurodegenerative Diseases (Q39071493) (← links)
- The prion model for progression and diversity of neurodegenerative diseases (Q39151589) (← links)
- Interactions of pathological proteins in neurodegenerative diseases (Q39236779) (← links)
- Neuron loss and degeneration in the progression of TDP-43 in frontotemporal lobar degeneration (Q40055403) (← links)
- Ante mortem cerebrospinal fluid tau levels correlate with postmortem tau pathology in frontotemporal lobar degeneration (Q40118660) (← links)
- Pathomechanisms and clinical aspects of frontotemporal lobar degeneration (Q40414517) (← links)
- Cognition and eating behavior in amyotrophic lateral sclerosis: effect on survival (Q40719786) (← links)
- Amyotrophic lateral sclerosis modifies progenitor neural proliferation in adult classic neurogenic brain niches (Q41624962) (← links)
- Cortical hyperexcitability in patients with C9ORF72 mutations: Relationship to phenotype (Q41818176) (← links)
- Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology (Q42501188) (← links)
- Distinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosis (Q42617513) (← links)