Sergio Sanabria

Dr. Sergio Sanabria

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Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 October 2018 in Physics in Medicine & Biology
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Journal Article
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SSSergio Sanabria
Sergio Sanabria
EÖEce Özkan
Ece Özkan
MRMarga Rominger
Marga Rominger
OGOrcun Goksel
Orcun Goksel
Despite many uses of ultrasound, some pathologies such as breast cancer still cannot reliably be diagnosed in either conventional B-mode ultrasound imaging nor with more recent ultrasound elastography methods. Speed-of-sound (SoS) is a quantitative imaging biomarker, which is sensitive to structural changes due to pathology, and hence could facilitate diagnosis. Full-angle ultrasound computed tomography (USCT) was proposed to obtain spatially-resolved SoS images, however, its water-bath setup involves practical limitations. To increase clinical utility and for widespread use, recently, a limited-angle Fourier-domain SoS reconstruction was proposed, however, it suffers from significant image reconstruction artifacts. In this work, we present a SoS reconstruction strategy, where the forward problem is formulated using differential time-of-flight measurements based on apparent displacements along different ultrasound wave propagation paths, and the inverse problem is solved in spatial-domain using a proposed total-variation scheme with spatially-varying anisotropic weighting to compensate for geometric bias from limited angle imaging setup. This is shown to be robust to missing displacement data and easily allow for incorporating any prior geometric information. In numerical simulations, SoS values in inclusions are accurately reconstructed with 90% accuracy up to a noise level of 50%. With respect to Fourier-domain reconstruction, our proposed method improved contrast ratio from 0.37 to 0.67 for even high noise levels such as 50%. Numerical full-wave simulation and our preliminary in vivo results illustrate the clinical applicability of our method in a breast cancer imaging setting. Our proposed method requires single-sided access to the tissue and can be implemented as an add-on to conventional ultrasound equipment, applicable to a range of transducers and applications.

27 September 2012 in Wood Science and Technology
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Journal Article
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TOTomasz Ozyhar
Tomasz Ozyhar
SHStefan Hering
Stefan Hering
SSSergio Sanabria
Sergio Sanabria
PNPeter Niemz
Peter Niemz

26 March 2019 in Investigative Radiology
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Journal Article
Closed access
LRLisa Ruby
Lisa Ruby
SSSergio Sanabria
Sergio Sanabria
KMKatharina Martini
Katharina Martini
KDKonstantin J. Dedes
Konstantin J. Dedes
DVDenise Vorburger
Denise Vorburger
MRMarga B. Rominger
Marga B. Rominger
Purpose: The aim of this study was to differentiate malignant and benign solid breast lesions with a novel ultrasound (US) technique, which measures speed of sound (SoS) using standard US transducers and intrinsic tissue reflections and scattering (speckles) as internal reference. Materials and Methods: This prospective, institutional review board–approved, Health Insurance Portability and Accountability Act-compliant prospective comparison study was performed with prior written informed consent from 20 women. Ten women with histological proven breast cancer and 10 with fibroadenoma were measured. A conventional US system with a linear probe was used for SoS-US (SonixTouch; Ultrasonix, Richmond, British Columbia, Canada). Tissue speckle reflections served as a timing reference for the US signals transmitted through the breasts. Relative phase inconsistencies were detected using plane wave measurements from different angular directions, and SoS images with 0.5-mm resolution were generated using a spatial domain reconstruction algorithm. The SoS of tumors were compared with the breast density of a larger cohort of 106 healthy women. Results: Breast lesions show focal increments ΔSoS (meters per second) with respect to the tissue background. Peak ΔSoS values were evaluated. Breast carcinoma showed significantly higher ΔSoS than fibroadenomas (∆SoS > 41.64 m/s: sensitivity, 90%; specificity, 80%; area under curve, 0.910) and healthy breast tissue of different densities (area under curve, 0.938; sensitivity, 90%; specificity, 96.5%). The lesion localization in SoS-US images was consistent with B-mode imaging and repeated SoS-US measurements were reproducible. Conclusions: Using SoS-US, based on conventional US and tissue speckles as timing reference, breast carcinoma showed significantly higher SoS values than fibroadenoma and healthy breast tissue of different densities. The SoS presents a promising technique for differentiating solid breast lesions.

25 August 2016 in Wood Science and Technology
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Journal Article
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EBErik Bachtiar
Erik Bachtiar
SSSergio Sanabria
Sergio Sanabria
JMJohannes P. Mittig
Johannes P. Mittig
PNPeter Niemz
Peter Niemz

10 December 2014 in Holzforschung
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Journal Article
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FBFranziska Baensch
Franziska Baensch
MZMichaela Zauner
Michaela Zauner
SSSergio Sanabria
Sergio Sanabria
MSMarkus G.R. Sause
Markus G.R. Sause
BPBernd R. Pinzer
Bernd R. Pinzer
PNPeter Niemz
Peter Niemz
Tensile tests of miniature spruce wood specimens have been performed to investigate the damage evolution in wood at the microscopic scale. For this purpose, the samples were stepwise tensile loaded in the longitudinal (L) and radial (R) directions and the damage evolution was monitored in real-time by acoustic emission (AE) and synchrotron radiation micro-computed tomography (SRμCT). This combination is of outstanding benefit as SRμCT monitoring provides an insight on the crack evolution and the final fracture at microscopic scale, whereas AE permits the detection of the associated accumulation and interaction of single damage events on all length scales with high time resolution. A significant drawback of the AE testing of wood has been overcome by means of calibrating the AE amplitudes with the underlying crack length development. Thus, a setup-dependent and wood species-dependent calibration value was estimated, which associates 1 μm2 crack area generating of 0.0038 mV in the detected AE amplitude. Furthermore, for both L and R specimens, AE signals were classified into two clusters by using a frequency-based approach of unsupervised pattern recognition. The shares of AE signals of both clusters correlate with the ratio of the relative crack area of the interwall and transwall cracks gained from the fractographic analysis of SRμCT scans.

15 October 2018 in European Radiology
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Journal Article
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SSSergio Sanabria
Sergio Sanabria
KMKatharina Martini
Katharina Martini
GFGregor Freystätter
Gregor Freystätter
LRLisa Ruby
Lisa Ruby
OGOrcun Goksel
Orcun Goksel
MRMarga B. Rominger
Marga B. Rominger