## Abstract This paper describes a new method for diffusion imaging of the human brain __in vivo__ that is based on a combination of diffusionβencoding gradients with highβspeed STEAM MR imaging. The singleβshot sequence 90Β°βTE/2β90Β°βTMβ(Ξ±βTE/2βSTE)~__n__~ generates __n__ = 32β64 differently phaseβ
On high b diffusion imaging in the human brain: ruminations and experimental insights
β Scribed by Robert V. Mulkern; Steven J. Haker; Stephan E. Maier
- Book ID
- 104060362
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 873 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0730-725X
No coin nor oath required. For personal study only.
β¦ Synopsis
Interest in the manner in which brain tissue signal decays with b factor in diffusion imaging schemes has grown in recent years following the observation that the decay curves depart from purely monoexponential decay behavior. Regardless of the model or fitting function proposed for characterizing sufficiently sampled decay curves (vide infra), the departure from monoexponentiality spells increased tissue characterization potential. The degree to which this potential can be harnessed to improve specificity, sensitivity and spatial localization of diseases in brain, and other tissues, largely remains to be explored. Furthermore, the degree to which currently popular diffusion tensor imaging methods, including visually impressive white matter fiber "tractography" results, have almost completely ignored the nonmonoexponential nature of the basic signal decay with b factor is worthy of communal introspection. Here we limit our attention to a review of the basic experimental features associated with brain water signal diffusion decay curves as measured over extended b-factor ranges, the simple few parameter fitting functions that have been proposed to characterize these decays and the more involved models, e.g.,"ruminations," which have been proposed to account for the nonmonoexponentiality to date.
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