Physically interpretable descriptors drive the materials design of metal hydrides for hydrogen storage. [PDF]
Chem SciJang SH +7 more
europepmc +1 more source
Use of Symptomatic Drug Treatment for Fatigue in Multiple Sclerosis and Patterns of Work Loss
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To describe the use of central stimulants and amantadine for fatigue in MS and evaluate a potential association with reduced work loss in people with MS. Methods We conducted a nationwide, matched, register‐based cohort study in Sweden (2006 to 2023) using national registers with prospective data collection.
Simon Englund +3 more
wiley +1 more source
Large-scale experimental investigation of the reliability of confidence measures. [PDF]
Commun PsycholBouleau C, Lebreton M, Jacquemet N.
europepmc +1 more source
Database Design and Relational Theory: Normal Forms and All That Jazz
, 2012 C. J. Date
semanticscholar +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
A Decade of Change in Sample Size and Study Setting in Leading Anesthesiology Journals: A Cross-Sectional Meta-Research Study. [PDF]
CureusTajima R +7 more
europepmc +1 more source
Design and Implementation of a Graphical User Interface for a Multimedia Database Management System
, 1992 Metin Balcı, Erhan Saridoğan
openalex +1 more source
Effectiveness and Safety of Nusinersen and Risdiplam in Spinal Muscular Atrophy: A Systematic Review
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Spinal Muscular Atrophy (SMA) is a rare genetic disorder marked by progressive muscle weakness and mobility loss. It has a profound physical, emotional and social impact on patients and caregivers, requiring comprehensive medical and supportive care.
Amin Mehrabian +9 more
wiley +1 more source
Prediction model of axial compressive bearing capacity of concrete-encased steel composite columns based on SHAP and machine learning. [PDF]
Sci RepWang J, Gong X, Chen J, Kan Z.
europepmc +1 more source
Design and Validation of the Novel Perso-Arabic Database in Shahmukhi Punjabi Script [PDF]
Humera Rafique, Tariq Javid
openalex +1 more source