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Pietro Ferraro
Researcher at National Research Council
Publications - 720
Citations - 14634
Pietro Ferraro is an academic researcher from National Research Council. The author has contributed to research in topics: Digital holography & Holography. The author has an hindex of 61, co-authored 653 publications receiving 12666 citations. Previous affiliations of Pietro Ferraro include Aeritalia & Centre national de la recherche scientifique.
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Label-free quantification of the effects of lithium niobate polarization on cell adhesion via holographic microscopy.
TL;DR: A label-free holographic total internal reflection microscopy technique is shown; the technique is able to evaluate quantitatively the contact area of live fibroblast cells adhering onto the surface of a ferroelectric lithium niobate crystal, and results show values of contact area significantly different between cells adhered to the positive or negative face of the crystal.
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Miscalibration-Tolerant Fourier Ptychography
TL;DR: The proposed method is non-iterative, fully parallelizable, and completely blind, unlocking the use of Fourier Ptychography as an easy to handle tool or add-on to existing microscopes to be employed by unskilled users, thus paving the way to biomedical and clinical practices.
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Hydrodynamic red blood cells deformation by quantitative phase microscopy and Zernike polynomials
TL;DR: It is demonstrated that new optical parameters of RBCs can be measured and analyzed thus opening the route to exploit the bio-lensing modeling as a new biomechanical marker of R BCs.
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Gravity driven high throughput phase detecting cytometer based on quantitative interferometric microscopy
TL;DR: In this paper, a simple large scale biological sample phase detection device called gravity driven high throughput phase detecting cytometer based on quantitative interferometric microscopy to obtain flowing red blood cells phase.
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Enhancing depth of focus in tilted microfluidics channels by digital holography.
TL;DR: It is shown that it is possible to improve the DOF and to recover the extended focus image of a tilted object in a single reconstruction step and the possibility of obtaining well-focused biological cells flowing into a tilted microfluidic channel is demonstrated.