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04014nam a2200589 4500 |
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978-3-540-45733-6 |
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20191026032146.0 |
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|a 9783540457336
|9 978-3-540-45733-6
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|a 10.1007/3-540-45733-X
|2 doi
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|a QD71-142
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|a 543
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|a Contrast Agents I
|h [electronic resource] :
|b Magnetic Resonance Imaging /
|c edited by Werner Krause.
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|a 1st ed. 2002.
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|a Berlin, Heidelberg :
|b Springer Berlin Heidelberg :
|b Imprint: Springer,
|c 2002.
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|a X, 249 p. 21 illus., 2 illus. in color.
|b online resource.
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|a text
|b txt
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|a computer
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|a Topics in Current Chemistry,
|x 0340-1022 ;
|v 221
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|a Extracellular MRI Contrast Agents Based on Gadolinium -- Structures of MRI Contrast Agents in Solution -- Relaxivity of MRI Contrast Agents -- Kinetic Stabilities of Gadolinium(III) Chelates Used as MRI Contrast Agents -- New Classes of MRI Contrast Agents -- Non-Gadolinium-Based MRI Contrast Agents -- Blood-Pool MRI Contrast Agents: Properties and Characterization.
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|a Extracellular MRI and X-ray contrast agents are characterized by their phar- cokinetic behaviour.After intravascular injection their plasma-level time curve is characeterized by two phases. The agents are rapidly distributed between plasma and interstitial spaces followed by renal elimination with a terminal half-live of approximatly 1-2 hours. They are excreted via the kidneys in unchanged form by glomerular filtration. Extracellular water-soluble contrast agents to be applied for X-ray imaging were introduced into clinical practice in 1923. Since that time they have proved to be most valuable tools in diagnostics.They contain iodine as the element of choice with a sufficiently high atomic weight difference to organic tissue. As positive contrast agents their attenuation of radiation is higher compared with the attenuation of the surrounding tissue. By this contrast enhancement X-ray diagnostics could be improved dramatically. In 2,4,6-triiodobenzoic acid derivatives iodine is firmly bound. Nowadays diamides of the 2,4,6-triiodo-5-acylamino-isophthalic acid like iopromide (Ultravist, Fig. 1) are used as non-ionic (neutral) X-ray contrast agents in most cases [1].
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|a Analytical chemistry.
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|a Physical chemistry.
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|a Organic chemistry.
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|a Materials science.
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|a Biochemistry.
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|a Laboratory medicine.
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|a Analytical Chemistry.
|0 http://scigraph.springernature.com/things/product-market-codes/C11006
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|a Physical Chemistry.
|0 http://scigraph.springernature.com/things/product-market-codes/C21001
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|a Organic Chemistry.
|0 http://scigraph.springernature.com/things/product-market-codes/C19007
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|a Characterization and Evaluation of Materials.
|0 http://scigraph.springernature.com/things/product-market-codes/Z17000
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|a Biochemistry, general.
|0 http://scigraph.springernature.com/things/product-market-codes/L14005
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|a Laboratory Medicine.
|0 http://scigraph.springernature.com/things/product-market-codes/B15007
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|a Krause, Werner.
|e editor.
|4 edt
|4 http://id.loc.gov/vocabulary/relators/edt
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|a SpringerLink (Online service)
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|t Springer eBooks
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|i Printed edition:
|z 9783642075964
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|i Printed edition:
|z 9783662146538
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|i Printed edition:
|z 9783540422471
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|a Topics in Current Chemistry,
|x 0340-1022 ;
|v 221
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|u https://doi.org/10.1007/3-540-45733-X
|z Full Text via HEAL-Link
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|a ZDB-2-CMS
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|a ZDB-2-BAE
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|a Chemistry and Materials Science (Springer-11644)
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