Results 51 to 60 of about 13,612 (265)

An Efficient Numerical Method Based on Bell Wavelets for Solving the Fractional Integro-Differential Equations with Weakly Singular Kernels

open access: yesFractal and Fractional
A novel numerical scheme based on the Bell wavelets is proposed to obtain numerical solutions of the fractional integro-differential equations with weakly singular kernels.
Yanxin Wang, Xiaofang Zhou
doaj   +1 more source

A Review on Harmonic Wavelets and Their Fractional Extension

open access: yesJournal of Advanced Engineering and Computation, 2018
In this paper a review on harmonic wavelets and their fractional generalization, within the local fractional calculus, will be discussed. The main properties of harmonic wavelets and fractional harmonic wavelets will be given, by taking into account of ...
Carlo Cattani
doaj   +1 more source

Five‐Year Disease Progression in Synuclein Seeding Positive Sporadic Parkinson's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To provide a comprehensive description of disease progression in synuclein seeding assay (SAA) positive sporadic Parkinson Disease participants, using Neuronal Synuclein Disease integrated biological and functional impairment staging framework.
Paulina Gonzalez‐Latapi   +19 more
wiley   +1 more source

A Prospective Study of Individuals at Risk of Multiple Sclerosis Informs the Design of Primary Prevention Studies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective In multiple sclerosis, the optimal time for deploying a therapeutic intervention is before the central nervous system is damaged; given the success of trials treating the earliest stage of MS, the radiologically isolated syndrome, developing primary prevention strategies is an important next challenge.
Amy W. Laitinen   +7 more
wiley   +1 more source

Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina   +11 more
wiley   +1 more source

Variation-Diminishing Wavelets and Wavelet Transforms

open access: yesReal Analysis Exchange, 2012
By using Schoenberg's theory of convolution transform variation, diminishing wavelets and wavelets of specific changes in sign are constructed. An inversion formula involving derivatives of the wavelet transform is also established. Wavelets generated by Tanno's form of convolution kernels and H-functions are also investigated.
openaire   +3 more sources

Wavelets on Fractals

open access: yesRevista Matemática Iberoamericana, 2006
We show that there are Hilbert spaces constructed from the Hausdorff measures \mathcal{H}^{s} on the real line \mathbb{R} with
Dorin E. Dutkay, Palle E.T. Jorgensen
openaire   +5 more sources

Epilepsy‐Associated Variants of a Single SCN1A Codon Exhibit Divergent Functional Properties

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Pathogenic variants in SCN1A, which encodes the voltage‐gated sodium channel NaV1.1, are associated with multiple epilepsy syndromes exhibiting a range of clinical severity. SCN1A variants are reported in different syndromes, including Dravet syndrome, which is associated with loss‐of‐function, whereas neonatal/infantile‐onset ...
Lanie N. Liebovitz   +3 more
wiley   +1 more source

Multidimensional Profiling of MRI‐Negative Temporal Lobe Epilepsy Uncovers Distinct Phenotypes

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Although hippocampal sclerosis (TLE‐HS) represents the most frequent cause of temporal lobe epilepsy (TLE), up to 30% of patients show no lesion on visual MRI inspection (TLE‐MRIneg). These cases pose diagnostic and therapeutic challenges and are underrepresented in surgical series.
Alice Ballerini   +28 more
wiley   +1 more source

Onasemnogene Abeparvovec in Type I Spinal Muscular Atrophy: 24‐Month Follow‐Up From the Italian Registry

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Onasemnogene abeparvovec (OA) is an AAV9‐based gene therapy for spinal muscular atrophy type I (SMA I). Real‐world outcomes show increased response variability compared to clinical trials, and follow‐up data beyond 12–18 months are limited.
Marika Pane   +43 more
wiley   +1 more source

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