Fracture Network Analysis Based on the Geologic Model of Channels. Part 1: Ideas and Computer Code.
, 1994 Tatsuya Tanaka +3 more
openalex +2 more sources
High-level networking with mobile code and first order AND-continuations [PDF]
, 2001 Paul Tarau, Verónica Dahl
openalex +1 more source
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco +18 more
wiley +1 more source
Attack Detection Using Network Coding in IoT Environment. [PDF]
Sensors (Basel), 2020 Lee Y, Lee GY.
europepmc +1 more source
Application of coding theory to interconnection networks
, 1992 Gilles Zémor, Gérard Cohen
openalex +1 more source
Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam +6 more
wiley +1 more source
An Adaptive Network Coding Scheme for Multipath Transmission in Cellular-Based Vehicular Networks. [PDF]
Sensors (Basel), 2020 Yin C +5 more
europepmc +1 more source
Decode to channel binary block codes based on neural networks and genetic algorithm [PDF]
, 2001 Yuanjin Zheng, Xiaoyan Tang, D.B.H. Tay
openalex +1 more source
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source
A hash-neighborhood-search-network-coding based opportunistic relay retransmission approach
Dianxin kexue, 2016 In wireless multicast networks，it is rarely concerned that there may be certain receiving nodes which have better quality links both to the source node and to the other receiving nodes.
Pengfei SHAO, Yanwei ZHAO, Zhaoxi FANG
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