The Interpretation of Carbon Nanotubes' Electrochemistry: Electrocatalysis and Mass Transport Regime in the Apparent Promotion of Electron Transfer. [PDF]
Dugeč J +5 more
europepmc +1 more source
Clinical Validation of Plasma p‐217tau in Neurological Diseases
ABSTRACT Objective Plasma p‐217tau is a minimally invasive but specific biomarker for diagnosing Alzheimer's disease (AD). However, its disease specificity remains to be clinically evaluated. We validated the reliability of the p‐217tau biomarker in 12 other neurological diseases.
Takeshi Kawarabayashi +13 more
wiley +1 more source
Localized mass transport channels for electro-upgrade of dilute CO<sub>2</sub> toward high-yield C<sub>2+</sub> products. [PDF]
Ren B +10 more
europepmc +1 more source
CSF Monoamine Metabolites and Cognitive Trajectory in Early Parkinson's Disease
ABSTRACT Background Imaging and postmortem studies indicate that abnormalities in monoaminergic neurotransmission contribute to cognitive impairment in Parkinson's disease (PD). However, it remains uncertain if cerebrospinal fluid (CSF) monoamine metabolites can serve as biomarkers of cognitive decline in early PD.
Jing‐Yu Shao +7 more
wiley +1 more source
Pseudo-two-dimensional multiphysics modeling of mass transport and pseudo-enzymatic kinetics in Ti<sub>3</sub>C<sub>2</sub>T <sub><i>x</i></sub> @Pt MXene-based glucose biosensors. [PDF]
Abu Shuheil M +8 more
europepmc +1 more source
SPG4 and Dementia: Expanding the Clinical Spectrum
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza +19 more
wiley +1 more source
Mesoporous Co-N-C Supported L1<sub>0</sub>-PtCo Alloy Enables Fast Mass Transport for Proton Exchange Membrane Fuel Cells. [PDF]
Nie Y +8 more
europepmc +1 more source
Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone +8 more
wiley +1 more source
Understanding the Current Distribution and Mass Transport Properties in 3D-Printed Architected Flow-Through Electrodes. [PDF]
Clemens AL +11 more
europepmc +1 more source

