Results 81 to 90 of about 2,054,309 (296)

Cognitive and Neuroimaging Divergence Between Juvenile and Adult FUS Amyotrophic Lateral Sclerosis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by progressive motor neuron degeneration. Fused in sarcoma (FUS)‐associated juvenile ALS (jALS) represents a distinct and aggressive subgroup with rapid deterioration and poor prognosis.
Alexandra V. Jürs   +7 more
wiley   +1 more source

Distance deterrence, trade barriers and accessibility. An analysis of market potential in the European Union

open access: yesEuropean Journal of Transport and Infrastructure Research, 2016
The interest in disentangling the role of borders in international trade is growing even within virtually borderless areas like the European Union. While there are a variety of research studies measuring how borders affect trade, there is little insight ...
María Henar Salas-Olmedo   +2 more
doaj   +1 more source

Decay of Electric Charge on Corona Charged Polyethylene

open access: yes, 2008
In this paper, the surface potential decay of corona-charged low density polyethylene (LDPE) films has been investigated. It has been found that for the same sample thickness the faster decay occurs in the sample with a higher charging voltage.
Xu, Zhiqiang   +2 more
core  

Parameters of the A1 → ϖπ decay

open access: yesNuclear Physics B, 1970
Abstract Combining the superconvergent sum rules for the A 1 ϱ → A 1 ϱ amplitude with the current algebraic “hard-pion” calculations of the related vertices given by Schnitzer and Weinberg, the solution δ = 0 has been found, implying a purely S-wave A 1 → ϱπ decay.
openaire   +1 more source

Deep Learning Pose Estimation for Phenotyping of Co‐Occurring Hyperkinetic Movement Disorders

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To explore whether routine outpatient video combined with deep learning‐based pose estimation and clinically interpretable kinematic features can support multi‐label phenotyping of co‐occurring hyperkinetic movement disorders (HMDs).
Laura Cif   +17 more
wiley   +1 more source

Natural Frequencies of Levodopa‐Induced Dyskinesia in Parkinson's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives Abnormal involuntary movements, known as dyskinesias, are common complications of levodopa treatment in patients with Parkinson's disease and can significantly impair quality of life. The underlying pathophysiology remains unclear, and current therapeutic options are limited.
Ioannis U. Isaias   +3 more
wiley   +1 more source

Probing a pseudoscalar at the LHC in light of muon g−2 and R(D(⁎)) excesses

open access: yesNuclear Physics B, 2017
We study the excesses of muon g−2 and R(D(⁎)) in the framework of a two-Higgs-doublet model with top quark flavor-changing neutral-current (FCNC) couplings.
Lei Wang, Jin Min Yang, Yang Zhang
doaj   +1 more source

Gravity‐Dependent Modulation of Downbeat Nystagmus: Insights From Velocity‐Storage Dysfunction

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Downbeat nystagmus varies with head position, a phenomenon termed gravity‐dependent modulation. We aimed to clarify its mechanism using a velocity‐storage model. Methods In 10 patients with downbeat nystagmus due to cerebellar disorders, we recorded eye movements at different pitch‐ and roll‐axis head positions.
Ji‐Hyung Park   +5 more
wiley   +1 more source

Study of χbJ(nP) → ωΥ(1S) via intermediate meson loop mechanism

open access: yesPhysics Letters B
In this work, we study the decays χbJ(2P) → ωΥ(1S) using the intermediate meson loop mechanism combined with an effective Lagrangian approach. Within the commonly adopted range of the form factor parameter α=0.8 to 4, the calculated decay widths are ...
Run-Hao Chen   +3 more
doaj   +1 more source

Validation of a Cellular Imaging‐Based Method as a Potential Biomarker for SPG4 Hereditary Spastic Paraplegia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Hereditary Spastic Paraplegia (HSP) comprises a group of rare genetic diseases characterized by length‐dependent axonal degeneration of the corticospinal tracts and dorsal columns, whose main clinical feature is spastic gait. Pathogenic variants in the SPG4 gene cause Spastic Paraplegia Type 4 (SPG4‐HSP), the most common form of HSP.
Gaia Fattorini   +12 more
wiley   +1 more source

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