Facilitating comprehensive child health monitoring within REDCap - an open-source code for real-time Z-score assessments. [PDF]
Mendon P+4 more
europepmc +1 more source
Reproducible Artificial Intelligence Research Requires Open Communication of Complete Source Code. [PDF]
Kitamura FC, Pan I, Kline TL.
europepmc +1 more source
Characteristics of Cerebral Palsy in the Midwestern US
ABSTRACT Objective Cerebral palsy (CP) is the most common lifelong motor disability worldwide. Yet, data is limited on how CP manifests in the US. Our objective was to characterize and determine factors affecting functional outcomes in a large population of young people with CP in the Midwestern US.
Susie Kim+6 more
wiley +1 more source
Advancing Dynamic-Time Warp Techniques for Correcting Eye Tracking Data in Reading Source Code. [PDF]
Al Madi N.
europepmc +1 more source
Low complexity sequential lossless coding for piecewise stationary memoryless sources [PDF]
Gil I. Shamir, N. Merhav
openalex +1 more source
ABSTRACT Background Managing long COVID in people with multiple sclerosis and related disorders (pwMSRD) is complex due to overlapping symptoms. To address evidence gaps, we evaluated long COVID susceptibility in pwMSRD versus controls and its associations with multi‐domain function and disability.
Chen Hu+15 more
wiley +1 more source
Moyamoya Disease and the Risk of Parkinson's Disease
ABSTRACT Objectives Moyamoya disease (MMD) is a rare cerebrovascular disorder characterized by the progressive narrowing of arteries at the base of the brain, forming abnormal collateral vascular networks. While vascular parkinsonism is noted in MMD, its link to Parkinson's disease (PD) has not been explored.
Dallah Yoo+9 more
wiley +1 more source
Web service QoS prediction using improved software source code metrics. [PDF]
Rangarajan S, Liu H, Wang H.
europepmc +1 more source
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
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
Leveraging autocatalytic reactions for chemical domain image classification. [PDF]
Arcadia CE+9 more
europepmc +1 more source