Results 121 to 130 of about 416,241 (289)
Improved non-Rake receiver based on two dimensional spread spectrum for WCDMA systems
Tongxin xuebao, 2005 A direct sequence spread spectrum receiver based on two dimensional spread spectrum for WCDMA systems was proposed. Unlike the conventional Rake receiver, the proposed receiver is motivated by idea of the transform domain design and makes full use of the
TANG You-xi +3 more
doaj +2 more sources
Reduced Muscular Carnosine in Proximal Myotonic Myopathy—A Pilot 1H‐MRS Study
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Myotonic dystrophy type 2 (proximal myotonic myopathy, PROMM) is a progressive multisystem disorder with muscular symptoms (proximal weakness, pain, myotonia) and systemic manifestations such as diabetes mellitus, cataracts, and cardiac arrhythmias.
Alexander Gussew +11 more
wiley +1 more source
AN INTERFERENCE-IMMUNE COMMUNICATION SYSTEM FOR DIGITAL DATA TRANSMISSION BASED ON A MULTI-CHANNEL CORRELATOR Part 2. DEVELOPMENT OF A CORRELATION-TYPE TRANSCEIVER BASED ON A MULTI-CHANNEL CORRELATOR [PDF]
Radio Physics and Radio AstronomySubject and Purpose. The objective of Part 2 of the work is the development and experimental study of a multichannel correlator for creating a correlation-type transceiver based on software-defined radio (SDR) systems.
A. V. Varavin +7 more
doaj
Spread Spectrum Data Transmission System for User Unmanned Aerial Vehicles
Transport and TelecommunicationIn today’s world of unmanned aerial vehicle (UAV) telecommunications, data transmission is both important and delicate. Various organizations have used special techniques to ensure reliable transmission and stable communication. At this stage, we propose
Zellal Somia +3 more
doaj +1 more source
Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder
Annals 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
Discovery and Targeted Proteomic Studies Reveal Striatal Markers Validated for Huntington's Disease
Annals 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
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective The Gold Coast criteria permit diagnosis of amyotrophic lateral sclerosis (ALS) even without upper motor neuron (UMN) signs. However, whether ALS patients with UMN signs (ALSwUMN) and those without (ALSwoUMN) share similar characteristics and prognoses remains unclear.
Hee‐Jae Jung +7 more
wiley +1 more source
Whole‐Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To characterize whole‐body intramuscular fat distribution pattern in patients with sarcoglycanopathies and explore correlations with disease severity, duration and age at onset. Methods Retrospective, cross‐sectional, multicentric study enrolling patients with variants in one of the four sarcoglycan genes who underwent whole‐body ...
Laura Costa‐Comellas +39 more
wiley +1 more source
Anti-interference Technology of VHF Voice Communication System and Its Development Trend
Kongzhi Yu Xinxi Jishu, 2019 Nowadays, with the increase in the number of flights, the number of stations is increasing, and electromagnetic interferences is becoming more and more serious.
WANG Qianying
doaj
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background SOX1 antibody‐positive paraneoplastic neurological syndromes (PNS) exhibit significant population‐specific clinical heterogeneity. While Western cohorts predominantly manifest Lambert‐Eaton myasthenic syndrome (65%–80%), comprehensive clinical characterization and treatment response data in Asian populations remain critically ...
Jin‐Long Ye +11 more
wiley +1 more source