The existence and location of a human counterpart of macaque visual area V4 are disputed. To resolve this issue, we used functional magnetic resonance imaging to obtain topographic maps from human subjects, using visual stimuli and tasks designed to maximize accuracy of topographic maps of the fovea and parafovea and to measure the effects of attention on topographic maps. We identified multiple topographic transitions, each clearly visible in Ն75% of the maps, that we interpret as boundaries of distinct cortical regions. We call two of these regions dorsal V4 and ventral V4 (together comprising human area V4) because they share several defining characteristics with the macaque regions V4d and V4v (which together comprise macaque area V4). Ventral V4 is adjacent to V3v, and dorsal V4 is adjacent to parafoveal V3d. Ventral V4 and dorsal V4 meet in the foveal confluence shared by V1, V2, and V3. Ventral V4 and dorsal V4 represent complementary regions of the visual field, because ventral V4 represents the upper field and a subregion of the lower field, whereas dorsal V4 represents lower-field locations that are not represented by ventral V4. Finally, attentional modulation of spatial tuning is similar across dorsal and ventral V4, but attention has a smaller effect in V3d and V3v and a larger effect in a neighboring lateral occipital region.

Post-OLT HCV recurrence can be safely treated with PEG-IFN and RIB. Bone marrow toxicity, depression, and rejection are limiting factors that require aggressive management. There was short-term histologic benefit to the use of this regimen, even in those patients without viral clearance.

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Functional magnetic resonance imaging (fMRI) suffers from many problems that make signal estimation difficult. These include variation in the hemodynamic response across voxels and low signal-to-noise ratio (SNR). We evaluate several analysis techniques that address these problems for event-related fMRI. (1) Many fMRI analyses assume a canonical hemodynamic response function, but this assumption may lead to inaccurate data models. By adopting the finite impulse response model, we show that voxel-specific hemodynamic response functions can be estimated directly from the data. (2) There is a large amount of low-frequency noise fluctuation (LFF) in blood oxygenation level dependent (BOLD) time-series data. To compensate for this problem, we use polynomials as regressors for LFF. We show that this technique substantially improves SNR and is more accurate than high-pass filtering of the data. (3) Model overfitting is a problem for the finite impulse response model because of the low SNR of the BOLD response. To reduce overfitting, we estimate a hemodynamic response timecourse for each voxel and incorporate the constraint of time-event separability, the constraint that hemodynamic responses across event types are identical up to a scale factor. We show that this technique substantially improves the accuracy of hemodynamic response estimates and can be computed efficiently. For the analysis techniques we present, we evaluate improvement in modeling accuracy via 10-fold cross-validation.