Results 21 to 30 of about 464,323 (316)

Lessons learned about [F-18]-AV-1451 off-target binding from an autopsy-confirmed Parkinson’s case

open access: yesActa Neuropathologica Communications, 2017
[F-18]-AV-1451 is a novel positron emission tomography (PET) tracer with high affinity to neurofibrillary tau pathology in Alzheimer’s disease (AD). PET studies have shown increased tracer retention in patients clinically diagnosed with dementia of AD ...
Marta Marquié   +15 more
doaj   +1 more source

Disruption of hippocampal neuronal circuit function depends upon behavioral state in the APP/PS1 mouse model of Alzheimer’s disease

open access: yesScientific Reports, 2022
The Alzheimer’s disease-associated peptide amyloid-beta (Aβ) has been associated with neuronal hyperactivity under anesthesia, but clinical trials of anticonvulsants or neural system suppressors have, so far, failed to improve symptoms in AD.
Heng Zhou   +5 more
doaj   +1 more source

Variation within the Huntington's disease gene influences normal brain structure. [PDF]

open access: yes, 2011
Genetics of the variability of normal and diseased brain structure largely remains to be elucidated. Expansions of certain trinucleotide repeats cause neurodegenerative disorders of which Huntington's disease constitutes the most common example. Here, we
Juliane Winkelmann   +40 more
core   +1 more source

Mushroom Natural Products in Neurodegenerative Disease Drug Discovery

open access: yes, 2022
The variety of drugs available to treat neurodegenerative diseases is limited. Most of these drug’s efficacy is restricted by individual genetics and disease stages and usually do not prevent neurodegeneration acting long after irreversible damage has ...
Evelin Tiralongo   +7 more
core   +1 more source

Neuronal SNCA transcription during Lewy body formation

open access: yesActa Neuropathologica Communications, 2023
Misfolded α-synuclein (α-syn) is believed to contribute to neurodegeneration in Lewy body disease (LBD) based on considerable evidence including a gene-dosage effect observed in relation to point mutations and multiplication of SNCA in familial Parkinson’
Tomoya Kon   +8 more
doaj   +1 more source

Sphingolipids in neurodegenerative diseases

open access: yesFrontiers in Neuroscience, 2023
Neurodegenerative Diseases (NDDs) are a group of disorders that cause progressive deficits of neuronal function. Recent evidence argues that sphingolipid metabolism is affected in a surprisingly broad set of NDDs. These include some lysosomal storage diseases (LSDs), hereditary sensory and autonomous neuropathy (HSAN), hereditary spastic paraplegia ...
Xueyang Pan   +8 more
openaire   +4 more sources

Slow motor neurons resist pathological TDP-43 and mediate motor recovery in the rNLS8 model of amyotrophic lateral sclerosis

open access: yesActa Neuropathologica Communications, 2022
In the intermediate stages of amyotrophic lateral sclerosis (ALS), surviving motor neurons (MNs) that show intrinsic resistance to TDP-43 proteinopathy can partially compensate for the loss of their more disease-susceptible counterparts.
Seong Kwon Hur   +8 more
doaj   +1 more source

Pros and cons of a prion-like pathogenesis in Parkinson's disease [PDF]

open access: yes, 2011
Background: Parkinson's disease (PD) is a slowly progressive neurodegenerative disorder which affects widespread areas of the brainstem, basal ganglia and cerebral cortex.
Chapman Joab   +10 more
core   +1 more source

Sex Differences in Stroke Subtypes, Severity, Risk Factors, and Outcomes Among Elderly Patients with Acute Ischemic Stroke

open access: yesFrontiers in Aging Neuroscience, 2015
Background: Although the age-specific incidence and mortality of stroke is higher among men, stroke has a greater clinical effect on women. However, the sex differences in stroke among elderly patients are unknown.
Changshen eYu   +7 more
doaj   +1 more source

Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage

open access: yesNature Communications, 2021
Knowledge of genomic features specific to humans may be important for understanding disease. Here the authors demonstrate a potential role for these human-lineage-specific sequences in brain development and neurological disease.
Zhongbo Chen   +13 more
doaj   +1 more source

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