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Matthias Stuber

Researcher at University of Lausanne

Publications -  388
Citations -  14724

Matthias Stuber is an academic researcher from University of Lausanne. The author has contributed to research in topics: Magnetic resonance imaging & Coronary artery disease. The author has an hindex of 59, co-authored 367 publications receiving 13620 citations. Previous affiliations of Matthias Stuber include University of Bordeaux & Brigham and Women's Hospital.

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Serum calcification propensity is associated with renal tissue oxygenation and resistive index in patients with arterial hypertension or chronic kidney disease.

TL;DR: In this paper, the underlying mechanisms linking arterial calcifications, vascular stiffness and renal function in patients with arterial hypertension (AH) and chronic kidney disease (CKD) were investigated.
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5D Flow MRI: A Fully Self-gated, Free-running Framework for Cardiac and Respiratory Motion-resolved 3D Hemodynamics.

TL;DR: A self-gated free-running whole-heart five-dimensional flow MRI framework consistently captured cardiac and respiratory motion-resolved 3D hemodynamics in less than 8 minutes.
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High-resolution selective three-dimensional magnetic resonance coronary angiography with navigator-echo technique: segment-by-segment evaluation of coronary artery stenosis.

TL;DR: To investigate the feasibility of high‐resolution selective three‐dimensional (3D) magnetic resonance coronary angiography (MRCA) in the evaluation of coronary artery stenoses, a high-resolution magnetic resonance imaging system is used.
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Practical signal‐to‐noise ratio quantification for sensitivity encoding: Application to coronary MR angiography

TL;DR: To develop and evaluate a practical method for the quantification of signal‐to‐noise ratio (SNR) on coronary MR angiograms (MRA) acquired with parallel imaging.
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Characterization of perfluorocarbon relaxation times and their influence on the optimization of fluorine‐19 MRI at 3 tesla

TL;DR: To characterize and optimize 19F MRI for different perfluorocarbons at 3T and quantify the loss of acquisition efficiency as a function of different temperature and cellular conditions.