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Methods of measuring spin-lattice (T1) relaxation times: An annotated bibliography

✍ Scribed by Kingsley, Peter B.


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
346 KB
Volume
11
Category
Article
ISSN
1043-7347

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✦ Synopsis


This review of methods of measuring spin-lattice T relaxation times 1 comprises 283 references, including 90 references on magnetic resonance imaging. Annotations give brief descriptions of each reference. References are organized by major categories, with cross-references to other topics. Major categories include many methods, optimization, data analysis, elimination of errors, signal intensity formulas, chemical exchange, and spatially localized measurements. Key references are indicated in several categories.


πŸ“œ SIMILAR VOLUMES


Determination of optimal angles for vari
✍ Sean C.L. Deoni; Terry M. Peters; Brian K. Rutt πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 204 KB πŸ‘ 1 views

## Abstract __T__~1~ and __T__~2~ can be rapidly determined with a combination of multiangle spoiled gradient recalled echo (SPGR) and steady‐state free precession (SSFP) imaging. Previously, we demonstrated a simple method for determining the set of SPGR and SSFP angles that provided greater __T__

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The goal of this work is to provide regional T(1) and T(2) values at a field strength of 7 T for the normal mouse brain at 6 weeks and 1 year old. A novel segmented snapshot FLASH sequence was used to measure T(1) in the hippocampus, corpus callosum, and the retrosplenial granular (RSG) cortex; T(2)

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1H NMR spin-lattice relaxation times (T1) of the N-CH3 proton resonances of phosphocreatine (PCr) and creatine (Cr) in water solutions were obtained using the 1,3,3,1 pulse sequence. These T1 values were equivalent to those obtained in D2O and water using either the conventional inversion-recovery e

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## Abstract __T__~1~relaxation times of PCr and β‐ATP in human cardiac and skeletal muscle were evaluated using a variable nutation method. This allows __T__~1~measurements with a constant TR and a significant reduction in acquisition time compared with the partial saturation method. Four 1D CSI da