Results 221 to 230 of about 4,550,803 (308)
Cellular porosity in dentin exhibits complex network characteristics with spatio-temporal fluctuations. [PDF]
Chatelain L +5 more
europepmc +1 more source
ABSTRACT Objective Cognitive impairment, fatigue, and depression are common in multiple sclerosis (MS), potentially due to disruption of regional functional connectivity caused by white matter (WM) lesions. We explored whether WM lesions functionally connected to specific brain regions contribute to these MS‐related manifestations.
Alessandro Franceschini +7 more
wiley +1 more source
Identifying Influential Nodes Based on Evidence Theory in Complex Network. [PDF]
Tan F +5 more
europepmc +1 more source
ABSTRACT Background Poststroke fatigue (PSF) and frailty share substantial overlap in their manifestations, yet previous research has yielded conflicting results due to the use of heterogeneous frailty assessment tools. Objective To evaluate the independent impact of frailty on PSF using a unified measurement system (Tilburg Frailty Indicator, TFI ...
Chuan‐Bang Chen +6 more
wiley +1 more source
Unveiling connectivity patterns of railway timetables through complex network theory and Infomap clustering. [PDF]
Lamanna F, Prisma M, Medeossi G.
europepmc +1 more source
Control Crisis in Financial Systems with Dynamic Complex Network Approach [PDF]
Hugo G. Venegas +6 more
openalex +1 more source
ABSTRACT Objective Epilepsy is increasingly associated with immune dysregulation and inflammation. The T cell receptor (TCR), a key mediator of adaptive immunity, shows repertoire alterations in various immune‐mediated diseases. The unique TCR sequence serves as a molecular barcode for T cells, and clonal expansion accompanied by reduced overall TCR ...
Yong‐Won Shin +12 more
wiley +1 more source
Closed-loop pathways associated with clinical symptoms in children with autism spectrum disorder: a complex network analysis. [PDF]
Wang Y +11 more
europepmc +1 more source
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
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
Enhanced complex network influential node detection through the integration of entropy and degree metrics with node distance. [PDF]
Shetty RD, M R, Shetty KR, T M.
europepmc +1 more source

