about
Quantitative assessment of cancer vascular architecture by skeletonization of high-resolution 3-D contrast-enhanced ultrasound images: role of liposomes and microbubblesNon-invasive parenchymal, vascular and metabolic high-frequency ultrasound and photoacoustic rat deep brain imaging.MRI tracking of macrophages labeled with glucan particles entrapping a water insoluble paramagnetic Gd-based agent.Combined high resolution NMR and 1H and 17O relaxometric study sheds light on the solution structure and dynamics of the lanthanide(III) complexes of HPDO3A.Paramagnetic lanthanide(III) complexes as pH-sensitive chemical exchange saturation transfer (CEST) contrast agents for MRI applications.A paramagnetic MRI-CEST agent responsive to lactate concentration.Lanthanide-loaded erythrocytes as highly sensitive chemical exchange saturation transfer MRI contrast agents.Novel pH-reporter MRI contrast agents.Ternary complexes between cationic GdIII chelates and anionic metabolites in aqueous solution: an NMR relaxometric study.Insights on the relaxation of liposomes encapsulating paramagnetic Ln-based complexes.Iopamidol: Exploring the potential use of a well-established x-ray contrast agent for MRI.A multinuclear NMR relaxometry study of ternary adducts formed between heptadentate Gd(III) chelates and L-lactate.Effect of the intracellular localization of a Gd-based imaging probe on the relaxation enhancement of water protons.Gd-enhanced MR images of substrates other than water.Highly shifted LIPOCEST agents based on the encapsulation of neutral polynuclear paramagnetic shift reagents.Determination of water permeability of paramagnetic liposomes of interest in MRI field.First ex-vivo MRI co-localization of two LIPOCEST agents.Development and validation of a smoothing-splines-based correction method for improving the analysis of CEST-MR images.NMR relaxometric investigations of solid lipid nanoparticles (SLN) containing gadolinium(III) complexes.Relaxometric evaluation of novel manganese(II) complexes for application as contrast agents in magnetic resonance imaging.Contrast agents for magnetic resonance angiographic applications: 1H and 17O NMR relaxometric investigations on two gadolinium(III) DTPA-like chelates endowed with high binding affinity to human serum albumin.Ln(III)-DOTAMGly complexes: a versatile series to assess the determinants of the efficacy of paramagnetic chemical exchange saturation transfer agents for magnetic resonance imaging applications.A R2/R1 ratiometric procedure for a concentration-independent, pH-responsive, Gd(III)-based MRI agent.From spherical to osmotically shrunken paramagnetic liposomes: an improved generation of LIPOCEST MRI agents with highly shifted water protons.A high relaxivity Gd(III)DOTA-DSPE-based liposomal contrast agent for magnetic resonance imaging.Osmotically shrunken LIPOCEST agents: an innovative class of magnetic resonance imaging contrast media based on chemical exchange saturation transfer.Pushing the sensitivity envelope of lanthanide-based magnetic resonance imaging (MRI) contrast agents for molecular imaging applications.Methods for an improved detection of the MRI-CEST effect.Chapter 10 - Lanthanide-loaded paramagnetic liposomes as switchable magnetically oriented nanovesicles.Encoding the frequency dependence in MRI contrast media: the emerging class of CEST agents.Large relaxivity enhancement of paramagnetic lipid nanoparticles by restricting the local motions of the Gd(III) chelates.Supramolecular protamine/Gd-loaded liposomes adducts as relaxometric protease responsive probes.Surface modification of PLGA nanospheres with Gd-DTPA and Gd-DOTA for high-relaxivity MRI contrast agents.Structure, stability and relaxivity of trinuclear triangular complexes.Nanoparticle-based chemical exchange saturation transfer (CEST) agents.Optimizing the high-field relaxivity by self-assembling of macrocyclic Gd(III) complexes.Novel stable dendrimersome formulation for safe bioimaging applications.The extraordinary ligand binding properties of human serum albumin.Gd(DOTP)5-outer-sphere relaxation enhancement promoted by nitrogen bases.Challenges for molecular magnetic resonance imaging.
P50
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P50
description
researcher
@en
wetenschapper
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հետազոտող
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name
Enzo Terreno
@ast
Enzo Terreno
@en
Enzo Terreno
@es
Enzo Terreno
@nl
type
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Enzo Terreno
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Enzo Terreno
@en
Enzo Terreno
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Enzo Terreno
@nl
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Enzo Terreno
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Enzo Terreno
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Enzo Terreno
@es
Enzo Terreno
@nl
P106
P1153
6701583943
P21
P31
P496
0000-0003-3800-566X