Ti Doping Decreases Mn and Ni Dissolution from High-Voltage LiNi0.5Mn1.5O4 Cathodes
Vaibhav Sharma +5 more
doaj +1 more source
Crystal engineering in IUCrJ: from `the' crystal structure to `a' crystal structure
Gautam R. Desiraju
doaj +1 more source
A dual-responsive cationic acridinium nanohoop: redox activity and acid/base-controlled reversible guest capture and release. [PDF]
Ming J +11 more
europepmc +1 more source
ABSTRACT Objective Onasemnogene abeparvovec (OA) is an AAV9‐based gene therapy for spinal muscular atrophy type I (SMA I). Real‐world outcomes show increased response variability compared to clinical trials, and follow‐up data beyond 12–18 months are limited.
Marika Pane +43 more
wiley +1 more source
Isomorphism in a Series of Five Homologous Compounds. [PDF]
Andotra A +13 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
Structural modification of functionalized carbazoles: from Z' = 1 to Z' = 6. [PDF]
Abualnaja M +4 more
europepmc +1 more source
Elevated Connectivity During Language Processing Is Associated With Cognitive Performance in SeLECTS
ABSTRACT Objective Self‐Limited Epilepsy with Centrotemporal Spikes (SeLECTS) is associated with language impairments despite seizures originating in the motor cortex, suggesting aberrant cross‐network interactions. Here we tested whether functional connectivity in SeLECTS during language tasks predicts language performance.
Wendy Qi +8 more
wiley +1 more source
Hydrochlorides, hydrates, hydronitrate, and an unanticipated hydrolysis product of famotidine. [PDF]
Weaver MC, Oliver AG, Barstis TLO.
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

