<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-18T19:10:23Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/38593" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/38593</identifier><datestamp>2026-06-11T15:03:41Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131022</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Joseph B. Mandeville.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Leite, Francisca Maria Pais Horta</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Harvard University--MIT Division of Health Sciences and Technology.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Harvard University--MIT Division of Health Sciences and Technology</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2008-11-10T19:51:22Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2008-11-10T19:51:22Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2007</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/38593</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">156908733</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (Ph. D.)--Harvard-MIT Division of Health Sciences and Technology, February 2007.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">"September 2006."</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">The main goal of this thesis was to systematically characterize the detection sensitivity, temporal response, and spatial resolution of IRON contrast for fMRI within the awake, behaving monkey. Understanding these issues provides insights into the physiology of the functional response to local changes in brain activity, enables researchers to optimize experimental designs, and delineates the advantages and limitations of neuroimaging within this important animal model. The injection of the iron oxide contrast agent (MION) provided a 9-fold increase in efficiency for block designs relatively to BOLD contrast. Because the hemodynamic response function acts as a low-pass filter on neural activation to attenuate the size of differential responses to alternate stimuli, this factor dropped to approximately 2 for rapidly presented stimuli. Detection efficiency for event-related stimulus designs for BOLD and IRON contrasts could be optimized using random or semi-random distributions for interstimulus intervals. Small increases in predictability could be traded for large gains in efficiency, particularly for the IRON method. A general linear model was successfully employed to describe IRON and BOLD impulse response functions. Both responses were accurately described by a bimodal exponential model with similar time constants, a fast (4.5 sec) and a slow (13.5 sec).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">(cont.) The slow response comprised 80% of IRON signal, and was responsible for the BOLD post-stimulus undershoot. It likely encompasses changes in post-arteriole blood volume. Optimized IRON activation maps do not show activation in draining veins or draining tissue, in contrast with BOLD contrast. To examine what happens at the level of small vessels and capillaries, we used point-image stimuli to measure IRON and BOLD point spread functions (PSF) in V1. We estimated an IRON PSF no larger than approximately 0.4 mm, and a BOLD PSF with twice the size. Severe image distortions arising from monkey's body motion outside of the field of view currently limit the achievable spatial resolution. Preliminary data suggests multi-shot EPI with navigators may be useful in improving image stability at higher resolution for IRON fMRI, which can employ short echo times to minimize phase variations, while achieving maximum efficiency by increasing the MION dose.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Francisca Maria Pais Horta Leite.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Ph.D.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">131 p.</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">M.I.T. theses are protected by 
copyright. They may be viewed from this source for any purpose, but 
reproduction or distribution in any format is prohibited without written 
permission. See provided URL for inquiries about permission.</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="uri" lang="en_US">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Harvard University--MIT Division of Health Sciences and Technology.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Detection power, temporal response, and spatial resolution of IRON fMRI in awake, behaving monkeys at 3 Tesla</dim:field>
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   	&lt;Title>Detection power, temporal response, and spatial resolution of IRON fMRI in awake, behaving monkeys at 3 Tesla&lt;/Title>
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   	&lt;PublicationDate>2007&lt;/PublicationDate>
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        	&lt;DisplayName>Leite, Francisca Maria Pais Horta&lt;/DisplayName>
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    &lt;Keyword>Harvard University--MIT Division of Health Sciences and Technology.&lt;/Keyword>
   	&lt;Abstract>The main goal of this thesis was to systematically characterize the detection sensitivity, temporal response, and spatial resolution of IRON contrast for fMRI within the awake, behaving monkey. Understanding these issues provides insights into the physiology of the functional response to local changes in brain activity, enables researchers to optimize experimental designs, and delineates the advantages and limitations of neuroimaging within this important animal model. The injection of the iron oxide contrast agent (MION) provided a 9-fold increase in efficiency for block designs relatively to BOLD contrast. Because the hemodynamic response function acts as a low-pass filter on neural activation to attenuate the size of differential responses to alternate stimuli, this factor dropped to approximately 2 for rapidly presented stimuli. Detection efficiency for event-related stimulus designs for BOLD and IRON contrasts could be optimized using random or semi-random distributions for interstimulus intervals. Small increases in predictability could be traded for large gains in efficiency, particularly for the IRON method. A general linear model was successfully employed to describe IRON and BOLD impulse response functions. Both responses were accurately described by a bimodal exponential model with similar time constants, a fast (4.5 sec) and a slow (13.5 sec).&lt;/Abstract>
   	&lt;Abstract>(cont.) The slow response comprised 80% of IRON signal, and was responsible for the BOLD post-stimulus undershoot. It likely encompasses changes in post-arteriole blood volume. Optimized IRON activation maps do not show activation in draining veins or draining tissue, in contrast with BOLD contrast. To examine what happens at the level of small vessels and capillaries, we used point-image stimuli to measure IRON and BOLD point spread functions (PSF) in V1. We estimated an IRON PSF no larger than approximately 0.4 mm, and a BOLD PSF with twice the size. Severe image distortions arising from monkey&amp;apos;s body motion outside of the field of view currently limit the achievable spatial resolution. Preliminary data suggests multi-shot EPI with navigators may be useful in improving image stability at higher resolution for IRON fMRI, which can employ short echo times to minimize phase variations, while achieving maximum efficiency by increasing the MION dose.&lt;/Abstract>
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