Results 121 to 130 of about 3,194,056 (379)

Stark-Effect Scattering in Rough Quantum Wells

open access: yes, 2011
A scattering mechanism stemming from the Stark-shift of energy levels by electric fields in semiconductor quantum wells is identified. This scattering mechanism feeds off interface roughness and electric fields, and modifies the well known 'sixth-power ...
Jana, Raj K., Jena, Debdeep
core   +1 more source

Exploring Nasal Structural‐Microbial Interactions in Multiple Sclerosis‐Associated Olfactory Impairment

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Olfactory dysfunction is frequently observed in patients with multiple sclerosis (MS); however, its underlying mechanisms remain poorly understood. To date, no studies have directly examined the nasal mucosal microbiota in MS. This study aimed to explore potential relationships among olfactory function, nasal microbiota composition,
Zidan Gao   +5 more
wiley   +1 more source

Partial Densities of States, Scattering Matrices, and Green's Functions

open access: yes, 1996
The response of an arbitrary scattering problem to quasi-static perturbations in the scattering potential is naturally expressed in terms of a set of local partial densities of states and a set of sensitivities each associated with one element of the ...
A. I. Baz'   +29 more
core   +2 more sources

The Diverse Neuromuscular Spectrum of VPS13A Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective VPS13A disease (chorea‐acanthocytosis) is a rare neurodegenerative disorder caused by biallelic variants in VPS13A, typically presenting with hyperkinetic movement disorders, while neuromuscular signs are often mild. The aim of the project was to investigate the frequency and severity of neuromuscular impairment in VPS13A disease ...
Anne Buchberger   +16 more
wiley   +1 more source

XYZ-polarisation analysis of diffuse magnetic neutron scattering from single crystals

open access: yes, 2010
Studies of diffuse magnetic scattering largely benefit from the use of a multi-detector covering wide scattering angles. Therefore, the different contributions to the diffuse scattering that originate from magnetic, nuclear coherent, and nuclear spin ...
Brückel Th   +5 more
core   +1 more source

The Impact of Tilburg Frailty on Poststroke Fatigue in First‐Ever Stroke Patients: A Cross‐Sectional Study With Unified Measurement Tools and Improved Statistics

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Poststroke fatigue (PSF) and frailty share substantial overlap in their manifestations, yet previous research has yielded conflicting results due to the use of heterogeneous frailty assessment tools. Objective To evaluate the independent impact of frailty on PSF using a unified measurement system (Tilburg Frailty Indicator, TFI ...
Chuan‐Bang Chen   +6 more
wiley   +1 more source

Characterization of Crystallographic Structures Using Bragg-Edge Neutron Imaging at the Spallation Neutron Source

open access: yesJournal of Imaging, 2017
Over the past decade, wavelength-dependent neutron radiography, also known as Bragg-edge imaging, has been employed as a non-destructive bulk characterization method due to its sensitivity to coherent elastic neutron scattering that is associated with ...
Gian Song   +16 more
doaj   +1 more source

Mu and Tau Neutrino Thermalization and Production in Supernovae: Processes and Timescales

open access: yes, 2000
We investigate the rates of production and thermalization of $\nu_\mu$ and $\nu_\tau$ neutrinos at temperatures and densities relevant to core-collapse supernovae and protoneutron stars.
A. Burrows   +25 more
core   +1 more source

Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco   +18 more
wiley   +1 more source

Home - About - Disclaimer - Privacy