Results 181 to 190 of about 44,708 (295)
Tracking Motor Progression and Device‐Aided Therapy Eligibility in Parkinson's Disease
ABSTRACT Objective To characterise the progression of motor symptoms and identify eligibility for device‐aided therapies in Parkinson's disease, using both the 5‐2‐1 criteria and a refined clinical definition, while examining differences across genetic subgroups.
David Ledingham +7 more
wiley +1 more source
Prediction of π-electronic energy and physical properties of benzenoid hydrocarbons using domination degree based entropies. [PDF]
Kuriachan G, Parthiban A.
europepmc +1 more source
The Mysterious Domination of Food/Drinking Water Contaminants and Adulterants in Bangladesh
Abdul Kader Mohiuddin
openalex +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
A multi layered encryption framework using intuitionistic fuzzy graphs and graph theoretic domination for secure communication networks. [PDF]
Meenakshi A +4 more
europepmc +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
Integrating Ecofeminism Into Canadian Nursing to Tackle Climate Change and Health Issues. [PDF]
Tremblay É, Harrisson S.
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
Ephaptic conduction molding memory engrams. [PDF]
Rabinovitch A +4 more
europepmc +1 more source

