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MR Angiography with a New Rapid Clearance Blood Pool Agent (P792)

✍ Scribed by Ruehm, Stefan G; Schmitz-Cristina, Heidi; Violas, Xavier; Corot, Claire; Debatin, Jörg F


Book ID
123199723
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
29 KB
Volume
9
Category
Article
ISSN
1076-6332

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MR angiography with a new rapid-clearanc
✍ Stefan G. Ruehm; Heidi Christina; Xavier Violas; Claire Corot; Jörg F. Debatin 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 641 KB

## Abstract The purpose of this study was to assess a new Gd‐based macromolecular intravascular contrast agent (P792, Vistarem®; Laboratoire Guerbet, Aulnay sous Bois, France) for MR angiography (MRA). P792 is a macrocyclic gadolinium compound based on a gadoterate meglumine structure substituted b

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An original MRI contrast agent, called P792, is described. P792 is a gadolinium macrocyclic compound based on a Gd-DOTA structure substituted by hydrophilic arms. The chemical structure of P792 has been optimized in order to provide (1) a high r 1 relaxivity in the clinical field for MRI: 29 mM -1 ×

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## Abstract The signal‐enhancing characteristics of a new monodisperse monogadolinated macromolecular MR contrast medium (P792) were evaluated for magnetic resonance angiography (MRA) of the coronary arteries. A total of 15 cardiac examinations were performed in pigs at 1.5 T using a 3D gradient‐ec

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## Abstract The diagnostic potential of a new rapid clearance blood pool contrast medium (P792; MW = 6.47 kDa) for the MR assessment of microvessel characteristics was assessed in 42 chemically‐induced breast tumors, with comparisons to albumin‐(Gd‐DTPA). Microvessel characteristics, including the

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✍ Philippe Robert; Xavier Violas; Robin Santus; Denis Le Bihan; Claire Corot 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 256 KB 👁 1 views

## Abstract ## Purpose To design an ideal first‐pass profile for MR angiography (MRA) by optimizing a multiphasic injection protocol based on two experimental animal models. ## Materials and Methods An equivalent contrast‐enhanced (CE) MRA injection protocol was developed with controlled injecti