Results 161 to 170 of about 22,970,744 (375)

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

open access: yesAnnals 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

Motor PHM on Edge Computing with Anomaly Detection and Fault Severity Estimation through Compressed Data Using PCA and Autoencoder

open access: yesMachine Learning and Knowledge Extraction
The motor is essential for manufacturing industries, but wear can cause unexpected failure. Predictive and health management (PHM) for motors is critical in manufacturing sites.
Jong Hyun Choi   +4 more
doaj   +1 more source

Scalable NMF via linearly optimized data compression. [PDF]

open access: yesProc SPIE Int Soc Opt Eng, 2023
Ha SM, Bani A, Sotiras A.
europepmc   +1 more source

Quantitative Assessment of Upper Limb Ataxia Using a Virtual Reality‐Based Evaluation System

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Cerebellar ataxia impairs coordination and balance, reducing quality of life. Conventional clinical scales, including the Scale for the Assessment and Rating of Ataxia (SARA) and the International Cooperative Ataxia Rating Scale (ICARS), are widely used to assess ataxia but are limited by subjectivity and inter‐rater variability ...
Masayuki Sato   +5 more
wiley   +1 more source

A Comprehensive Overview of the Clinical, Electrophysiological, and Neuroimaging Features of BPAN: Insights From a New Case Series

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Neurodegeneration with brain iron accumulation (NBIA) comprises a genetically and clinically heterogeneous group of rare neurological disorders characterized particularly by iron accumulation in the basal ganglia. To date, 15 genes have been associated with NBIA.
Seda Susgun   +95 more
wiley   +1 more source

A trajectory data compression algorithm based on spatio-temporal characteristics. [PDF]

open access: yesPeerJ Comput Sci, 2022
Zhong Y   +5 more
europepmc   +1 more source

Potential benefits of delta encoding and data compression for HTTP [PDF]

open access: bronze, 1997
Jeffrey C. Mogul   +3 more
openalex   +1 more source

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