Results 51 to 60 of about 163,010 (261)

Doe wel en zie niet om: alzheimer tast beslissen tot vrijgevigheid niet aan

open access: yesTijdschrift voor Gerontologie en Geriatrie, 2010
bespreking Bosch-Domènech, A., Nagel, R.,& Sánchez-Andrés, J. V. (2010). Prosocial capabilities in Alzheimer’s patients. Journal of Gerontology: Social Sciences, 65B, 119-128.
Han F. A. Diesfeldt
doaj   +1 more source

Complementarity of Long‐Reads and Optical Mapping in Parkinson's Disease for Structural Variants

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Long‐read sequencing and optical genome mapping technologies have the ability to detect large and complex structural variants. This has led to the discovery of novel pathogenic variants in neurodegenerative movement disorders. Thus, we aimed to systematically compare the SV detection capabilities of OGM and ONT in Parkinson's disease.
André Fienemann   +17 more
wiley   +1 more source

Larrea tridentata Extract Mitigates Oxidative Stress-Induced Cytotoxicity in Human Neuroblastoma SH-SY5Y Cells

open access: yesAntioxidants, 2019
Creosote bush (Larrea tridentata; LT) leaves extracts were tested for their potential efficacy to mitigate cellular oxidative stress on human SH-SY5Y cells. Here, the differential nuclear staining assay, a bioimager system, and flow cytometric protocols,
Karla Morán-Santibañez   +7 more
doaj   +1 more source

Posterior Cortical Atrophy in the Asia‐Pacific: A Report From the PCA Asian Workgroup

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Posterior Cortical Atrophy (PCA) is a distinct dementia syndrome primarily affecting spatial abilities and visual processing. It is associated with degeneration in the posterior part of the brain. PCA is subclassified into PCA‐pure and PCA‐plus syndromes based on consensus criteria.
Yuttachai Likitjaroen   +11 more
wiley   +1 more source

Alzheimer's or alzheimer-perusini's disease?

open access: yesEuropean Psychiatry, 2007
For persons who suffer from Alzheimer's disease little changed since 1906, when Alois Alzheimer (Kraepelin's assistant) communicated to Psychiatric Convention of Tubinga the “Auguste D case”. Auguste had been affected by an unknown type of dementia. After case presentation, no discussion followed.
G.L. Conte, M. Pomponi
openaire   +1 more source

Synaptic and metabolic gene expression alterations in neurons that are recipients of proteopathic tau seeds

open access: yesActa Neuropathologica Communications, 2020
Recent studies suggest that misfolded tau molecules can be released, and taken up by adjacent neurons, propagating proteopathic seeds across neural systems.
Marta Perez-Rando   +5 more
doaj   +1 more source

Paramagnetic Rim Lesions Are Associated With Trans‐Synaptic Degeneration of the Visual Pathway in Multiple Sclerosis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives Retrograde trans‐synaptic degeneration (rTSD) from posterior visual pathway lesions in multiple sclerosis (MS) is characterized by hemi‐macular ganglion cell‐inner plexiform layer (GCIPL) thinning and contralateral visual field loss.
Abdul Jaber Tayem   +17 more
wiley   +1 more source

Review of Postgraduate Dissertations on Alzheimer's Patients in Nursing Care

open access: yesYaşlı Sorunları Araştırma Dergisi
Increasingly, health problems have started to occur in the increasing elderly population. The physical and psychological problems that occur with aging have brought the search for new care and treatment methods to the agenda, and with the increase in ...
Fadime Toru
doaj   +1 more source

Clinical Validation of Plasma p‐217tau in Neurological Diseases

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Plasma p‐217tau is a minimally invasive but specific biomarker for diagnosing Alzheimer's disease (AD). However, its disease specificity remains to be clinically evaluated. We validated the reliability of the p‐217tau biomarker in 12 other neurological diseases.
Takeshi Kawarabayashi   +13 more
wiley   +1 more source

SPG4 and Dementia: Expanding the Clinical Spectrum

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza   +19 more
wiley   +1 more source

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