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Dive into the research topics where Roger C. Grimm is active.

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Featured researches published by Roger C. Grimm.


Magnetic Resonance in Medicine | 2004

In vivo visualization of Alzheimer's amyloid plaques by magnetic resonance imaging in transgenic mice without a contrast agent.

Clifford R. Jack; Michael Garwood; Thomas M. Wengenack; Bret Borowski; Geoffrey L. Curran; Joseph Lin; Gregor Adriany; Olli Gröhn; Roger C. Grimm; Joseph F. Poduslo

One of the cardinal pathologic features of Alzheimers disease (AD) is the formation of senile, or amyloid, plaques. Transgenic mice have been developed that express one or more of the genes responsible for familial AD in humans. Doubly transgenic mice develop “human‐like” plaques, providing a mechanism to study amyloid plaque biology in a controlled manner. Imaging of labeled plaques has been accomplished with other modalities, but only MRI has sufficient spatial and contrast resolution to visualize individual plaques noninvasively. Methods to optimize visualization of plaques in vivo in transgenic mice at 9.4 T using a spin echo sequence based on adiabatic pulses are described. Preliminary results indicate that a spin echo acquisition more accurately reflects plaque size, while a T2* weighted gradient echo sequence reflects plaque iron content, not plaque size. In vivo MRI–ex vivo MRI–in vitro histologic correlations are provided. Histologically verified plaques as small as 50 μm in diameter were visualized in living animals. To our knowledge this work represents the first demonstration of noninvasive in vivo visualization of individual AD plaques without the use of a contrast agent. Magn Reson Med 52:1263–1271, 2004.


Magnetic Resonance in Medicine | 2002

Continuously moving table data acquisition method for long FOV contrast‐enhanced MRA and whole‐body MRI

David G. Kruger; Stephen J. Riederer; Roger C. Grimm; Phillip J. Rossman

A method is presented in which an extended longitudinal field of view (FOV), as required for whole‐body MRI or MRA peripheral runoff studies, is acquired in one seamless image. Previous methods typically either acquired 3D data at multiple static “stations” which covered the extended FOV or as a series of 2D axial sections. The method presented here maintains the benefits of 3D acquisition while removing the discrete nature of the multistation method by continuous acquisition of MR data as the patient table moves through the desired FOV. Although the technique acquires data only from a homogeneous central volume of the magnet at any point in time, by spatially registering all data it is possible to extend the FOV well beyond this volume. The method is demonstrated experimentally with phantoms, in vivo angiographic animal studies, and in vivo human studies. Magn Reson Med 47:224–231, 2002.


Magnetic Resonance in Medicine | 2000

Prospective multiaxial motion correction for fMRI

Heidi A. Ward; Stephen J. Riederer; Roger C. Grimm; Richard L. Ehman; Joel P. Felmlee; Clifford R. Jack

Corruption of the image time series due to interimage head motion limits the clinical utility of functional MRI. This paper presents a method for real‐time prospective correction of rotation and translation in all six degrees of rigid body motion. By incorporating an orbital navigator (ONAV) echo for each of the sagittal, axial, and coronal planes into the fMRI pulse sequence, rotation and translation can be measured and the spatial orientation of the image acquisition sequence that follows can be corrected prospectively in as little as 160 msec. Testing of the method using a computerized motion phantom capable of performing complex multiaxial motion showed subdegree rotational and submillimeter translational accuracy over a range of ±8° and ±8 mm of motion. In vivo images demonstrate correction of simultaneous through‐plane and in‐plane motion and improved detection of fMRI activation in the presence of head motion. Magn Reson Med 43:459–469, 2000.


American Journal of Roentgenology | 2009

Feasibility of In Vivo MR Elastographic Splenic Stiffness Measurements in the Assessment of Portal Hypertension

Jayant A. Talwalkar; Meng Yin; Sudhakar K. Venkatesh; Phillip J. Rossman; Roger C. Grimm; Armando Manduca; Anthony J. Romano; Patrick S. Kamath; Richard L. Ehman

OBJECTIVE Liver stiffness is associated with portal hypertension in patients with chronic liver disease. However, the relation between spleen stiffness and clinically significant portal hypertension remains unknown. The purposes of this study were to determine the feasibility of measuring spleen stiffness with MR elastography and to prospectively test the technique in healthy volunteers and in patients with compensated liver disease. MATERIALS AND METHODS Spleen stiffness was measured with MR elastography in 12 healthy volunteers (mean age, 37 years; range, 25-82 years) and 38 patients (mean age, 56 years; range, 36-60 years) with chronic liver disease of various causes. For patients with liver disease, laboratory findings, spleen size, presence and size of esophageal varices, and liver histologic results were recorded. Statistical analyses were performed to assess all measurements. RESULTS MR elastography of the spleen was successfully performed on all volunteers and patients. The mean spleen stiffness was significantly lower in the volunteers (mean, 3.6 +/- 0.3 kPa) than in the patients with liver fibrosis (mean, 5.6 +/- 5.0 kPa; range, 2.7-19.2 kPa; p < 0.001). In addition, a significant correlation was observed between liver stiffness and spleen stiffness for the entire cohort (r(2) = 0.75; p < 0.001). Predictors of spleen stiffness were splenomegaly, spleen volume, and platelet count. A mean spleen stiffness of 10.5 kPa or greater was identified in all patients with esophageal varices. CONCLUSION MR elastography of the spleen is feasible and shows promise as a quantitative method for predicting the presence of esophageal varices in patients with advanced hepatic fibrosis.


Neurogastroenterology and Motility | 2009

Application of Magnetic Resonance Imaging to Measure Fasting and Postprandial Volumes in Humans

Jeff L. Fidler; Adil E. Bharucha; Michael Camilleri; Jon J. Camp; Duane Burton; Roger C. Grimm; Stephen J. Riederer; Richard A. Robb; Alan R. Zinsmeister

Abstract  Our aims were to measure the gastric volume response in excess of ingested meal volume (i.e. gastric accommodation), contribution of swallowed air to this excess, day‐to‐day variability of gastric volumes measured by MRI and their relationship to volumes measured by single‐photon‐emission computed tomography (SPECT). In 20 healthy volunteers, fasting and postprandial gastric volumes were measured after technetium99m‐pertechnetate labeling of the gastric mucosa by SPECT and separately by MRI, using 3D gradient echo and 2D half‐Fourier acquisition single‐shot turbo spin echo (HASTE) sequences. Ten of these subjects had a second MRI exam to assess intra‐individual variation. Thereafter, another 10 subjects had two MRI studies during which they ingested the nutrient in 30 or 150 mL aliquots. During MRI, the postprandial gastric volume change exceeded the ingested meal volume by 106 ± 12 mL (Mean ± SEM). The HASTE and gradient echo sequences distinguished air from fluid under fasting and postprandial conditions respectively. This postprandial excess mainly comprised air (61 ± 5 mL), which was not significantly different when ingested as 30 or 150 mL aliquots. Fasting and postprandial gastric volumes measured by MRI were generally reproducible within subjects. During SPECT, postprandial volumes increased by 158 ± 18 mL; gastric volumes measured by SPECT were higher than MRI. MRI measures gastric volumes with acceptable performance characteristics; the postprandial excess primarily consists of air, which is not affected by the mode of ingestion. Gastric volumes are technique specific and differ between MRI and SPECT.


Investigative Radiology | 2013

Magnetic resonance elastography noninvasively detects in vivo renal medullary fibrosis secondary to swine renal artery stenosis

Michael J. Korsmo; Behzad Ebrahimi; Alfonso Eirin; John R. Woollard; James D. Krier; John A. Crane; Lizette Warner; Kevin J. Glaser; Roger C. Grimm; Richard L. Ehman; Lilach O. Lerman

ObjectivesMagnetic resonance elastography (MRE) can noninvasively sample tissue stiffness in vivo. Renal fibrosis secondary to renal artery stenosis (RAS), which is aggravated in atherosclerotic RAS (ARAS), may increase its stiffness. An increase in cortical stiffness in vivo can be masked by intrinsic hemodynamic determinants, whereas renal medullary stiffness is less dependent on renal hemodynamics. Therefore, this study tested the hypothesis that MRE-determined medullary stiffness would correspond to the histological degree of medullary fibrosis in stenotic kidneys in RAS and detect its exacerbation in ARAS. Materials and MethodsSeventeen pigs were studied 10 weeks after induction of unilateral RAS (n = 6), ARAS (n = 5), or sham (n = 6). Stiffness of the cortex and the medulla was determined through 3-dimensional MRE, and renal perfusion and function were determined using multidetector computed tomography. Kidney fibrosis was subsequently assessed ex vivo using the Masson trichrome staining. ResultsRenal stenotic cortex and medulla were significantly more fibrotic in RAS and ARAS compared with healthy kidney. However, MRE detected increased stiffness in RAS compared with the healthy kidney (12.7 ± 0.41 kPa vs 10.7 ± 0.18 kPa; P = 0.004) only in the medulla, which was further increased in ARAS (16.6 ± 1.3 kPa; P = 0.017 vs RAS). Magnetic resonance elastography–derived medullary, but not cortical, stiffness significantly correlated with histological degree of fibrosis, although cortical and medullary fibroses were correlated. Renal blood flow and function were similarly decreased in RAS and ARAS compared with the healthy kidney. ConclusionsNoninvasive 3-dimensional MRE detects increased renal medullary stiffness in RAS and ARAS in vivo, which correlates with its fibrosis ex vivo and may also reflect cortical fibrosis. Hence, MRE-derived medullary stiffness can be potentially useful in detecting renal fibrosis and track disease progression.


Magnetic Resonance in Medicine | 2006

Needle shear wave driver for magnetic resonance elastography

Q. C C Chan; Geng Li; Richard L. Ehman; Roger C. Grimm; R. Li; E. S. Yang

Magnetic resonance elastography (MRE) is capable of quantitatively depicting the mechanical properties of tissues in vivo. In contrast to mechanical excitation at the surface of the tissue, the method proposed in this study describes shear waves produced by an inserted needle. The results demonstrate that MRE performed with the needle driver provides shear stiffness estimates that correlate well with those obtained using mechanical testing. Comparisons between MRE acquisitions obtained with surface and needle drivers yielded similar results in general. However, the well‐defined wave propagation pattern provided by the needle driver in a target region can reduce section orientation‐related error in wavelength estimation that occurs with surface drivers in 2D MRE acquisitions. Preliminary testing of the device was performed on animals. This study demonstrates that the needle driver is an effective option that offers advantages over surface drivers for obtaining accurate stiffness estimates in targeted regions that are accessible by the needle. Magn Reson Med, 2006.


Neurogastroenterology and Motility | 2011

GASTRIC MOTOR DISTURBANCES IN PATIENTS WITH IDIOPATHIC RAPID GASTRIC EMPTYING

Adil E. Bharucha; Armando Manduca; David S. Lake; Jeff L. Fidler; Phillip Edwards; Roger C. Grimm; Alan R. Zinsmeister; Stephen J. Riederer

Background  The mechanisms of ‘idiopathic’ rapid gastric emptying, which are associated with functional dyspepsia and functional diarrhea, are not understood. Our hypotheses were that increased gastric motility and reduced postprandial gastric accommodation contribute to rapid gastric emptying.


Journal of Magnetic Resonance Imaging | 2011

High temporal and spatial resolution 3D time-resolved contrast-enhanced magnetic resonance angiography of the hands and feet

Clifton R. Haider; Stephen J. Riederer; Eric A. Borisch; James F. Glockner; Roger C. Grimm; Thomas C. Hulshizer; Thanila A. Macedo; Petrice M. Mostardi; Phillip J. Rossman; Terri J. Vrtiska; Phillip M. Young

Methods are described for generating 3D time‐resolved contrast‐enhanced magnetic resonance (MR) angiograms of the hands and feet. Given targeted spatial resolution and frame times, it is shown that acceleration of about one order of magnitude or more is necessary. This is obtained by a combination of 2D sensitivity encoding (SENSE) and homodyne (HD) acceleration methods. Image update times from 3.4–6.8 seconds are provided in conjunction with view sharing. Modular receiver coil arrays are described which can be designed to the targeted vascular region. Images representative of the technique are generated in the vasculature of the hands and feet in volunteers and in patient studies. J. Magn. Reson. Imaging 2011;.


Magnetic Resonance in Medicine | 2004

Interscan registration using navigator echoes

Edward Brian Welch; Armando Manduca; Roger C. Grimm; Clifford R. Jack

A common problem in clinical MRI is anatomic misalignment of imaging slices across successive examinations. This unnecessarily complicates the radiologic assessment of anatomic change over time on serial MRI studies. To address this problem, spherical navigator echoes, which can detect rigid body motion in all six degrees of freedom, were used to guide spatial location and orientation adjustments to an exam prescription to match the reference frame of images acquired in an earlier exam. An initial linear navigator echo is also necessary to effect coarse Z translation adjustments prior to fine six degrees of freedom adjustment with a spherical navigator echo. Results of this technique are presented for head image volumes of five volunteers. Each volunteer was imaged on two scanners. In all cases, the reference frame adjustments provided by the navigator echoes substantially improved the alignment of the latter exam and performed well compared to retrospective image‐based registration. Magn Reson Med 52:1448–1452, 2004.

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