Results 131 to 140 of about 577,663 (312)

Clinical Impact of NOTCH3 Variant Location After First Stroke in CADASIL

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Despite its monogenic origin, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy exhibits marked variability in clinical expression and severity. Variants in the NOTCH3 gene, within epidermal growth factor‐like repeat domains 1–6 or 7–34, are known to influence disease onset, but their impact ...
Léa Aguilhon   +5 more
wiley   +1 more source

A GPT-reinforced social robot for patient communication: a pilot study

open access: yesFrontiers in Digital Health
ProblemQuality healthcare requires effective patient communication. However, lack of personnel and increasing demands on healthcare professionals (HCPs) create a need for innovative solutions that enhance accessibility and delivery of information to ...
Jan-Willem J. R. van 't Klooster   +12 more
doaj   +1 more source

WRC-07: the Technological and Market Pressures for Flexible Spectrum Access

open access: yes
By examining the preparations for the 2007 ITU World Radio Conference (WRC-07) and associated developments this paper identifies practical examples of the market and technological pressures contributing towards a more liberalised approach to spectrum ...
Sims, Martin
core  

Management Strategies of Patients with Neuromyelitis Optica Spectrum Disorder During the COVID-19 Pandemic Era

open access: yes, 2020
Sherif M Hamdy, Maged Abdel-Naseer, Hatem S Shehata, Nevin M Shalaby, Amr Hassan, Alaa Elmazny, Ehab Shaker, Mona AF Nada, Sandra M Ahmed, Mohamed I Hegazy, Husam S Mourad, Ahmed Abdelalim, Rehab Magdy, Alshimaa S Othman, Doaa A Mekkawy, Nirmeen A Kishk ...
Nada MAF   +15 more
core  

Strategic issues in national spectrum management [PDF]

open access: yes, 1989
The demand for allocations and assignments in the radio frequency spectrum continues to grow in the United States and internationally. The unique properties of the spectrum combined with this growing demand have created a significant managment ...
Allen, Tracy Scott
core  

Efficacy of Inebilizumab in N‐MOmentum Trial Participants With or Without Prior Immunosuppressants

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This post hoc analysis examined the impact of prior immunosuppressants on the long‐term efficacy and safety of inebilizumab, a cluster of differentiation 19+ B‐cell–depleting monoclonal antibody, in participants with aquaporin‐4–seropositive neuromyelitis optica spectrum disorder from the N‐MOmentum trial (NTC02200770).
Bruce A. C. Cree   +9 more
wiley   +1 more source

PICT-Net: A Transformer-Based Network with Prior Information Correction for Hyperspectral Image Unmixing

open access: yesRemote Sensing
Transformers have performed favorably in recent hyperspectral unmixing studies in which the self-attention mechanism possesses the ability to retain spectral information and spatial details.
Yiliang Zeng   +3 more
doaj   +1 more source

Spectrum management of ADSL

open access: yesElectronics Letters, 2002
The cumulative emission field resulting from the large-scale deployment of asynchronous digital subscriber line (ADSL) is determined using the model introduced by Papatsoris and Flintoft (see ibid., vol.36, no.13, p.1171-2, 2000) and the implications on medium frequency broadcasting are assessed.
openaire   +1 more source

A reassessment of minority overrepresentation in Connecticut's juvenile justice system : submitted to State of Connecticut, Office of Policy and Management, Policy Development and Planning Division /

open access: yes, 2001
Cover title.; "June 5, 2001."; Accompanied by appendices.; Includes bibliographical references (p. [10]).; " ... supported, in part, by grants from the Office of Juvenile Justice and Delinquency Prevention (OJJDP), Office of Justice Programs, U.S ...
Hartstone, Eliot C.
core  

A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
wiley   +1 more source

Home - About - Disclaimer - Privacy