ArticleJournal of biomedical optics2012
Snapshot spectrally encoded fluorescence imaging through a fiber bundle.
Article in Journal of biomedical optics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
7 citing papers in PubMed.
- Snapshot spectral imaging: from spatial-spectral mapping to metasurface-based imaging.Nanophotonics (Berlin, Germany) · 2024Review
- Image computing for fibre-bundle endomicroscopy: A review.Medical image analysis · 2020Review
- High-resolution endomicroscopy with a spectrally encoded miniature objective.Biomedical optics express · 2019Article
- 3D printed fiber optic faceplates by custom controlled fused deposition modeling.Optics express · 2018Article
- Fiber pattern removal and image reconstruction method for snapshot mosaic hyperspectral endoscopic images.Biomedical optics express · 2018Article
- All-passive pixel super-resolution of time-stretch imaging.Scientific reports · 2017Article
- High spatial sampling light-guide snapshot spectrometer.Optical engineering (Redondo Beach, Calif.) · 2017Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Fiber optic endomicroscopy is a valuable tool for clinical diagnostics and animal studies because it can capture images of tissue in vivo with subcellular resolution. Current configurations for endomicroscopes have either limited spatial resolution or require a scanning mechanism at the distal end of the fiber, which can slow imaging speed and increase the probe size. We present a novel configuration that provides high contrast 350 × 350 pixel images at 7.2 frames per second, without the need for mechanical scanning at the proximal or distal end of the fiber. The proof-of-concept benchtop system is tested in fluorescence mode and can resolve 1.5 µm features of a high resolution 1951 USAF target.
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Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.