Results 171 to 180 of about 4,848,832 (374)
The burden of burnout: Understanding its prevalence and organizational drivers in medical physics
Journal of Applied Clinical Medical Physics, EarlyView.Abstract Background Burnout is a work‐related syndrome characterized by increased levels of emotional exhaustion (EE) and depersonalization (DP) along with decreased levels of personal achievement. In the healthcare setting, higher burnout levels have been associated with negative impacts on personnel, an increased risk of errors, and a decrease in the
Deborah Schofield +4 more
wiley +1 more source
Localization accuracy of 6‐second CBCT for lung IGRT with various breathing patterns
Journal of Applied Clinical Medical Physics, EarlyView.Abstract Purpose The 6‐second cone beam computed tomography (CBCT) acquisition of the Ethos HyperSight (Varian Medical Systems, Inc. Palo Alto, CA, USA) on‐board imaging system offers benefits, but could be too fast to accurately capture an average target position in a free‐breathing lung cancer patient. This study aimed to ascertain whether a 6‐second
Jihye Koo +5 more
wiley +1 more source
Commentary: MSH3 homology and potential recombination link to SARS-CoV-2 furin cleavage site
Frontiers in Virology, 2022 Yseulys Dubuy, Hugo Lachuer
doaj +1 more source
Progressive Myoclonus Epilepsy: Distinctive MRI Changes in Cerebellar and Motor Networks
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Progressive myoclonus epilepsy (PME) is a rare generalized epilepsy syndrome with a well‐characterized genetic basis. The brain networks that are affected to give rise to the distinctive symptoms of PME are less well understood. Methods Eleven individuals with PME with a confirmed genetic diagnosis and 22 controls were studied.
Jillian M. Cameron +3 more
wiley +1 more source
Early Language Impairment as an Integral Part of the Cognitive Phenotype in Huntington's Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Huntington's disease (HD) speech/language disorders have typically been attributed to motor and executive impairment due to striatal dysfunction. In‐depth study of linguistic skills and the role of extrastriatal structures in HD is scarce.
Arnau Puig‐Davi +13 more
wiley +1 more source
The principle of general localization on unit sphere
Journal of Mathematical Analysis and Applications, 2009 AbstractIn this paper we study the general localization principle for Fourier–Laplace series on unit sphere SN⊂RN+1. Weak type (1,1) property of maximal functions is used to establish the estimates of the maximal operators of Riesz means at critical index N−12.
openaire +2 more sources
On breakdown of solutions of a constrained gradient system of total variation
Boletim da Sociedade Paranaense de Matemática, 2004 A gradient system of total variation is considered for a mapping fromthe unit disk to the unit sphere in R^3. For a class of initial data it is shown that a solution of its Dirichlet problem loses its smoothness in finite time.
Hirotoshi Kuroda, Yoshikazu Giga
doaj
Gap phenomenon of an abstract Willmore type functional of hypersurface in unit sphere. [PDF]
ScientificWorldJournal, 2014 Zhu Y, Liu J, Wu G.
europepmc +1 more source
Correspondence of MRI and nTMS With EDSS in Multiple Sclerosis: Longitudinal Follow‐Up Study
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objectives Considering the characteristics of multiple sclerosis (MS) disease and its impact on motor disability, this study aims to assess the functional integrity of the corticospinal tract by examining motor evoked potentials (MEPs), Expanded Disability Status Scale (EDSS) scores, magnetic resonance imaging (MRI) lesion counts, and ...
Antonia Bralić +13 more
wiley +1 more source
HPDL Variant Type Correlates With Clinical Disease Onset and Severity
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Recently, a mitochondrial encephalopathy due to biallelic HPDL variants was described, associated with a broad range of clinical manifestations ranging from severe, infantile‐onset neurodegeneration to adolescence‐onset hereditary spastic paraplegia. HPDL converts 4‐hydroxyphenylpyruvate acid (4‐HPPA) into 4‐hydroxymandelate (4‐HMA),
Eun Hye Lee +19 more
wiley +1 more source