Results 111 to 120 of about 523,662 (284)

Random linear fountain code with improved decoding success probability [PDF]

open access: yes2016 22nd Asia-Pacific Conference on Communications (APCC), 2016
This paper appears in: Communications (APCC), 2016 22nd Asia-Pacific Conference ...
openaire   +2 more sources

Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives We describe the clinical manifestations and developmental abilities of individuals with SYT1‐associated neurodevelopmental disorder (Baker‐Gordon syndrome) from infancy to adulthood. We further describe the neuroradiological and electrophysiological characteristics of the condition at different ages, and explore the associations ...
Sam G. Norwitz   +3 more
wiley   +1 more source

A Design of Overlapped Chunked Code over Compute-and-Forward for Multi-Source Multi-Relay Networks

open access: yesSensors, 2018
This paper investigates the design of overlapped chunked codes (OCC) for multi-source multi-relay networks where a physical-layer network coding approach, compute-and-forward (CF) based on nested lattice codes (NLC), is applied for the simultaneous ...
Rithea Ngeth   +3 more
doaj   +1 more source

Functional Connectivity Linked to Cognitive Recovery After Minor Stroke

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Patients with minor stroke exhibit slowed processing speed and generalized alterations in functional connectivity involving frontoparietal cortex (FPC). The pattern of connectivity evolves over time. In this study, we examine the relationship of functional connectivity patterns to cognitive performance, to determine ...
Vrishab Commuri   +7 more
wiley   +1 more source

Rethinking the Intercept Probability of Random Linear Network Coding

open access: yesIEEE Communications Letters, 2015
IEEE Communications Letters, to ...
Khan, Amjad Saeed   +2 more
openaire   +5 more sources

Discovery and Targeted Proteomic Studies Reveal Striatal Markers Validated for Huntington's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Clinical trials for Huntington's disease (HD) enrolling persons before clinical motor diagnosis (CMD) lack validated biomarkers. This study aimed to conduct an unbiased discovery analysis and a targeted examination of proteomic biomarkers scrutinized by clinical validation. Methods Cerebrospinal fluid was obtained from PREDICT‐HD and
Daniel Chelsky   +8 more
wiley   +1 more source

Glymphatic Dysfunction Reflects Post‐Concussion Symptoms: Changes Within 1 Month and After 3 Months

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mild traumatic brain injury (mTBI) may alter glymphatic function; however, its progression and variability remain obscure. This study examined glymphatic function following mTBI within 1 month and after 3 months post‐injury to determine whether variations in glymphatic function are associated with post‐traumatic symptom severity ...
Eunkyung Kim   +3 more
wiley   +1 more source

Importance of feature selection stability in the classifier evaluation on high-dimensional genetic data [PDF]

open access: yesPeerJ
Classifiers trained on high-dimensional data, such as genetic datasets, often encounter situations where the number of features exceeds the number of objects. In these cases, classifiers typically rely on a small subset of features.
Tomasz Łukaszuk, Jerzy Krawczuk
doaj   +2 more sources

Weight spectra of random linear codes

open access: yes, 2013
Weight spectra of random equiprobable linear codes over GF(p) are con- cerned. For a random linear code over GF(p) we derive explicit formulae for expectation and variance of number of vectors with fixed weight; bounds of the distribution of minimal weight of non-zero vectors are also obtained.
Zubkov, A. M., Kruglov, V. I.
openaire   +1 more source

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron   +5 more
wiley   +1 more source

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