Results 81 to 90 of about 3,604,186 (292)

Diffusion Spectrum Imaging Maps Early Axonal Loss and a Unique Progressive Signal in Neuronal Intranuclear Inclusion Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To delineate specific in vivo white matter pathology in neuronal intranuclear inclusion disease (NIID) using diffusion spectrum imaging (DSI) and define its clinical relevance. Methods DSI was performed on 42 NIID patients and 38 matched controls.
Kaiyan Jiang   +10 more
wiley   +1 more source

‘The Radical Black Colour’. On the Semantics of the Black Colour in Anarchist Discourse

open access: yesСлово.ру: балтийский акцент, 2017
The subject of this paper is the semantics of the colour black in anarchism. The author analyses the sociocultural and ontological aspects of the colour black as a symbol of anarchist criticism of power and the state.
Martynov M.
doaj   +1 more source

Dilatonic BTZ black holes with power-law field

open access: yes, 2017
Motivated by low energy effective action of string theory and large applications of BTZ black holes, we will consider minimal coupling between dilaton and nonlinear electromagnetic fields in three dimensions.
Hendi, S. H.   +3 more
core   +2 more sources

Fluid Biomarkers of Disease Burden and Cognitive Dysfunction in Progressive Supranuclear Palsy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Identifying objective biomarkers for progressive supranuclear palsy (PSP) is crucial to improving diagnosis and establishing clinical trial and treatment endpoints. This study evaluated fluid biomarkers in PSP versus controls and their associations with regional 18F‐PI‐2620 tau‐PET, clinical, and cognitive outcomes.
Roxane Dilcher   +10 more
wiley   +1 more source

A comparison of the fast timing behaviour of 4U 1705-44 to that of 4U 1608-52 and Cyg X-1 [PDF]

open access: yes, 1998
We studied the fast timing behaviour of the atoll source 4U 1705-44 using the entire EXOSAT dataset, four observations covering a total of 230,000 seconds of 1-20 keV spectral and timing data. In one of the observations, 4U 1705-44 was in a low intensity
Berger, M., van der Klis, M.
core   +1 more source

FDG‐PET Associations With Disease Severity and Outcomes in NMDA‐Receptor IgG Autoimmune Encephalitis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Patients with N‐methyl‐D‐aspartate (NMDA) receptor‐immunoglobulin G (IgG) autoimmune encephalitis (NMDAR‐IgG AE) demonstrate occipital lobe hypometabolism on baseline brain fluorodeoxyglucose‐positron emission tomography (bFDG‐PET).
Jonathan K. Lee   +7 more
wiley   +1 more source

Two-Stage Black-Start Optimization for Power Systems with Multi-Energy Microgrid as a Black-Start Unit

open access: yesShanghai Jiaotong Daxue xuebao
To reduce the losses caused by major power outages in power systems, a two-stage optimization method for black start of power systems is proposed using a multi-energy microgrid (MEMG) as a black-start source.
ZHU Yongqing, CHEN Changming, LI Qingsheng, LI Zhen, ZHANG Zhaofeng, LIN Zhenzhi
doaj   +1 more source

Black Religion and Black Power: The Nation of Islam’s Internationalism

open access: yesGenealogy, 2019
The Nation of Islam’s influence has extended beyond the United States. This Black American Muslim movement has used the intersection of race and religion to construct a blueprint of liberation that has bonded people of African descent throughout ...
Bayyinah S. Jeffries
doaj   +1 more source

Black-body components in Gamma-Ray Bursts spectra?

open access: yes, 2007
We study 7 Gamma Ray Bursts (GRBs), detected both by the BATSE instrument, on-board the Compton Gamma Ray Observatory, and by the Wide Field Camera (WFC), on-board BeppoSAX.
Bosnjak, Z.   +4 more
core   +3 more sources

Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce   +72 more
wiley   +1 more source

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