Results 101 to 110 of about 10,640,447 (355)

CSF Levels of NPTX2 Are Associated With Less Brain Atrophy Over Time in Cognitively Unimpaired Individuals

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Neuronal pentraxin 2 (NPTX2) is a synaptic protein involved in synaptic plasticity and regulation of neuronal excitability. Lower baseline cerebrospinal fluid (CSF) NPTX2 levels have been shown to be associated with an earlier onset of mild cognitive impairment (MCI), a pre‐dementia syndrome, even after CSF Alzheimer's Disease (AD)
Juan P. Vazquez   +12 more
wiley   +1 more source

Plasma Proteomic Signatures for Alzheimer's Disease: Comparable Accuracy to ATN Biomarkers and Cross‐Platform Validation

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background There is growing recognition of the potential of plasma proteomics for Alzheimer's Disease (AD) risk assessment and disease characterization. However, differences between proteomics platforms introduce uncertainties regarding cross‐platform applicability.
Manyue Hu   +9 more
wiley   +1 more source

Remarks on an Identity of Anastase and Díaz-Barrero

open access: yesAxioms
We extend an algebraic identity of Anastase and Díaz-Barrero (2022) and apply our results to deduce various formulas for sums and series involving (among others) Fibonacci and Lucas numbers, Bernoulli polynomials, and the Riemann zeta function.
Horst Alzer, Robert Frontczak
doaj   +1 more source

Finite summation formulas involving binomial coefficients, harmonic numbers and generalized harmonic numbers [PDF]

open access: yesJournal of Inequalities and Applications, 2013
zbMATH Open Web Interface contents unavailable due to conflicting licenses.
openaire   +1 more source

Acoustic Measures Capture Speech Dysfunction in Spinocerebellar Ataxia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinocerebellar ataxias (SCA) are hereditary cerebellar degenerative disorders with a common feature of dysarthria, involving impaired phonatory and articulatory control of speech, thereby affecting social communication. In this study, we investigated whether acoustic measures could objectively measure speech dysfunction and identify
Zena Fadel   +5 more
wiley   +1 more source

On the Range of Arithmetic Means of the Fractional Parts of Harmonic Numbers

open access: yesMathematics
In this paper, the limit points of the sequence of arithmetic means 1n∑m=1n{Hm}σ for n=1,2,3,… are studied, where Hm is the mth harmonic number with fractional part {Hm} and σ is a fixed positive constant.
Artūras Dubickas
doaj   +1 more source

On the number of roots for harmonic trinomials [PDF]

open access: green, 2021
Gerardo Barrera   +2 more
openalex   +1 more source

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron   +5 more
wiley   +1 more source

Binomial Series Involving Harmonic-like Numbers

open access: yesAxioms
By computing definite integrals, we shall examine binomial series of convergence rate ±1/2 and weighted by harmonic-like numbers. Several closed formulae in terms of the Riemann and Hurwitz zeta functions as well as logarithm and polylogarithm functions ...
Chunli Li, Wenchang Chu
doaj   +1 more source

Shared Genetic Effects and Antagonistic Pleiotropy Between Multiple Sclerosis and Common Cancers

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Epidemiologic studies have reported inconsistent altered cancer risk in individuals with multiple sclerosis (MS). Factors such as immune dysregulation, comorbidities, and disease‐modifying therapies may contribute to this variability.
Asli Buyukkurt   +5 more
wiley   +1 more source

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