Results 111 to 120 of about 15,052 (259)

Modelling of impulse loading in high-temperature superconductors. Assessment of accuracy and performance of computational techniques.

open access: yes, 2010
Purpose – The aim of this paper is to access performance of existing computational techniques to model strongly non-linear field diffusion problems. Design/methodology/approach – Multidimensional application of a finite volume front-fixing method to ...
Golosnoy, Igor O., Sykulski, Jan K.
core  

Advances in plasma spraying technology for coatings: from particle flight to splat formation

open access: yes工程科学学报
Plasma spraying technology plays a crucial role in coating preparation owing to its high efficiency and versatility. This technology heats and accelerates the spraying powder of metals, ceramics, polymers, and their composites through ultra-high ...
Kun LIU   +5 more
doaj   +1 more source

Feasibility and Tolerability of Performing Portable MRI for Neurological Disorders in an Outpatient Neurology Clinic: A Prospective Cohort

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Accessing brain magnetic resonance imaging (MRI) can be challenging, especially for underserved patients, which may lead to disparities in neurological diagnosis. Method This mixed‐methods study enrolled adults with one of four neurological disorders: mild cognitive impairment or dementia of the Alzheimer type, multiple sclerosis ...
Maya L. Mastick   +19 more
wiley   +1 more source

Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone   +8 more
wiley   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

Dimethyl Fumarate, But Not Rituximab, Reduces Serum GFAP Levels and PIRMA in Relapsing–Remitting MS

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Serum neurofilament light chain (sNfL) and glial fibrillary acidic protein (sGFAP) levels are believed to reflect mainly acute and chronic disease processes in multiple sclerosis (MS), respectively. In this study, we investigated whether dimethyl fumarate (DMF) and rituximab (RTX) differentially affect these biomarkers.
F. Shawket   +14 more
wiley   +1 more source

THE ACOUSTICS OF AUTOMOTIVE MUFFLERS: 1D-3D BEM ANALYSES, EXPERIMENTAL VALIDATION AND OPTIMIZATION

open access: yes, 2011
A number of numerical and experimental studies, performed in the field of technical flow duct acoustics, are presented in this thesis. The analyses have been implemented on the automotive mufflers, and the fluid-dynamic aspects have been taken into ...
Auriemma, Fabio
core  

The Challenge of Modeling High Speed Flows [PDF]

open access: yes, 2007
Current and expected developments in space transportation have led to growing interest in new space vehicles. These new vehicles require essential improvements over current vehicles in order to ensure economic viability and to fullfill mission and safety
Hannemann, K.   +2 more
core  

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach   +23 more
wiley   +1 more source

A Numerical study of resistance in a rough walled channel flow where the ratio of roughness length scale to the depth of flow varies over a wide range [PDF]

open access: yes, 2009
Numerical calculations were performed over a variety of two-dimensional rib roughness configurations in which the ratio of flow depth to roughness height was varied from 1.1 to 40.
Senior, A K
core  

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