Monolithic silicon nitride electro-optic modulator enabled by optically-assisted poling. [PDF]
Lafforgue C, Zabelich B, Brès CS.
europepmc +1 more source
Abstract Objective Exploring the prevalence and association between intracranial atherosclerosis (ICAS) and cerebral small vessel diseases (CSVD), this study delved beyond the current scope, utilising high‐resolution vessel wall MRI (HRVW‐MRI) to investigate how subtle changes in intracranial atherosclerotic features influence the various burdens of ...
Joseph Amihere Ackah+6 more
wiley +1 more source
Towards simultaneous imaging of ultrafast nuclear and electronic dynamics in small molecules. [PDF]
Mhatre S+4 more
europepmc +1 more source
Capturing what matters: Patient‐reported LGI1‐ANTibody encephalitis outcome RatiNg scale (LANTERN)
Abstract Background LGI1‐antibody encephalitis (LGI1‐Ab‐E) is a common form of autoimmune encephalitis where most patients demonstrate ‘good’ clinician‐rated outcomes. However, more targeted questionnaires reveal numerous debilitating symptoms for many years.
Mark J Kelly+9 more
wiley +1 more source
LumaCam: a novel class of position-sensitive event mode particle detectors using scintillator screens. [PDF]
Wolfertz A+11 more
europepmc +1 more source
Epitaxial (Ba,Sr)TiO3 Ferroelectric Thin Films for Integrated Optics
Doumon N.Y, S. Li
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Amygdala Neurodegeneration: A Key Driver of Visual Dysfunction in Parkinson's Disease
ABSTRACT Objective Visual disability in Parkinson's disease (PD) is not fully explained by retinal neurodegeneration. We aimed to delineate the brain substrate of visual dysfunction in PD and its association with retinal thickness. Methods Forty‐two PD patients and 29 controls underwent 3‐Tesla MRI, retinal spectral‐domain optical coherence tomography,
Asier Erramuzpe+15 more
wiley +1 more source
Universal conservation law governing the wave-particle duality and quantum entanglement. [PDF]
Sun K, Xu JS, Li CF.
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Progressive Myoclonus Epilepsy: Distinctive MRI Changes in Cerebellar and Motor Networks
ABSTRACT Objective Progressive myoclonus epilepsy (PME) is a rare generalized epilepsy syndrome with a well‐characterized genetic basis. The brain networks that are affected to give rise to the distinctive symptoms of PME are less well understood. Methods Eleven individuals with PME with a confirmed genetic diagnosis and 22 controls were studied.
Jillian M. Cameron+3 more
wiley +1 more source
Light People: Prof. Juejun Hu, exploring the light. [PDF]
Sun T.
europepmc +1 more source