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Dive into the research topics where Peter M. Jakob is active.

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Featured researches published by Peter M. Jakob.


Magnetic Resonance in Medicine | 2002

Generalized autocalibrating partially parallel acquisitions (GRAPPA)

Mark A. Griswold; Peter M. Jakob; Robin M. Heidemann; Mathias Nittka; Vladimir Jellus; Jianmin Wang; Berthold Kiefer; Axel Haase

In this study, a novel partially parallel acquisition (PPA) method is presented which can be used to accelerate image acquisition using an RF coil array for spatial encoding. This technique, GeneRalized Autocalibrating Partially Parallel Acquisitions (GRAPPA) is an extension of both the PILS and VD‐AUTO‐SMASH reconstruction techniques. As in those previous methods, a detailed, highly accurate RF field map is not needed prior to reconstruction in GRAPPA. This information is obtained from several k‐space lines which are acquired in addition to the normal image acquisition. As in PILS, the GRAPPA reconstruction algorithm provides unaliased images from each component coil prior to image combination. This results in even higher SNR and better image quality since the steps of image reconstruction and image combination are performed in separate steps. After introducing the GRAPPA technique, primary focus is given to issues related to the practical implementation of GRAPPA, including the reconstruction algorithm as well as analysis of SNR in the resulting images. Finally, in vivo GRAPPA images are shown which demonstrate the utility of the technique. Magn Reson Med 47:1202–1210, 2002.


Magnetic Resonance in Medicine | 2000

Partially Parallel Imaging With Localized Sensitivities (PILS)

Mark A. Griswold; Peter M. Jakob; Mathias Nittka; James W. Goldfarb; Axel Haase

In this study a novel partially parallel acquisition method is presented, which can be used to accelerate image acquisition using an RF coil array for spatial encoding. In this technique, Parallel Imaging with Localized Sensitivities (PILS), it is assumed that the individual coils in the array have localized sensitivity patterns, in that their sensitivity is restricted to a finite region of space. Within the PILS model, a detailed, highly accurate RF field map is not needed prior to reconstruction. In PILS, each coil in the array is fully characterized by only two parameters: the center of coils sensitive region in the FOV and the width of the sensitive region around this center. In this study, it is demonstrated that the incorporation of these coil parameters into a localized Fourier transform allows reconstruction of full FOV images in each of the component coils from data sets acquired with a reduced number of phase encoding steps compared to conventional imaging techniques. After the introduction of the PILS technique, primary focus is given to issues related to the practical implementation of PILS, including coil parameter determination and the SNR and artifact power in the resulting images. Finally, in vivo PILS images are shown which demonstrate the utility of the technique. Magn Reson Med 44:602–609, 2000.


Topics in Magnetic Resonance Imaging | 2004

SMASH, SENSE, PILS, GRAPPA How to Choose the Optimal Method

Martin Blaimer; Felix A. Breuer; Matthias F. Mueller; Robin M. Heidemann; Mark A. Griswold; Peter M. Jakob

Fast imaging methods and the availability of required hardware for magnetic resonance tomography (MRT) have significantly reduced acquisition times from about an hour down to several minutes or seconds. With this development over the last 20 years, magnetic resonance imaging (MRI) has become one of the most important instruments in clinical diagnosis. In recent years, the greatest progress in further increasing imaging speed has been the development of parallel MRI (pMRI). Within the last 3 years, parallel imaging methods have become commercially available, and therefore are now available for a broad clinical use. The basic feature of pMRI is a scan time reduction, applicable to nearly any available MRI method, while maintaining the contrast behavior without requiring higher gradient system performance. Because of its faster image acquisition, pMRI can in some cases even significantly improve image quality. In the last 10 years of pMRI development, several different pMRI reconstruction methods have been set up which partially differ in their philosophy, in the mode of reconstruction as well in their advantages and drawbacks with regard to a successful image reconstruction. In this review, a brief overview is given on the advantages and disadvantages of present pMRI methods in clinical applications, and examples from different daily clinical applications are shown.


Magnetic Resonance in Medicine | 2005

Controlled aliasing in parallel imaging results in higher acceleration (CAIPIRINHA) for multi-slice imaging.

Felix A. Breuer; Martin Blaimer; Robin M. Heidemann; Matthias F. Mueller; Mark A. Griswold; Peter M. Jakob

In all current parallel imaging techniques, aliasing artifacts resulting from an undersampled acquisition are removed by means of a specialized image reconstruction algorithm. In this study a new approach termed “controlled aliasing in parallel imaging results in higher acceleration” (CAIPIRINHA) is presented. This technique modifies the appearance of aliasing artifacts during the acquisition to improve the subsequent parallel image reconstruction procedure. This new parallel multi‐slice technique is more efficient compared to other multi‐slice parallel imaging concepts that use only a pure postprocessing approach. In this new approach, multiple slices of arbitrary thickness and distance are excited simultaneously with the use of multi‐band radiofrequency (RF) pulses similar to Hadamard pulses. These data are then undersampled, yielding superimposed slices that appear shifted with respect to each other. The shift of the aliased slices is controlled by modulating the phase of the individual slices in the multi‐band excitation pulse from echo to echo. We show that the reconstruction quality of the aliased slices is better using this shift. This may potentially allow one to use higher acceleration factors than are used in techniques without this excitation scheme. Additionally, slices that have essentially the same coil sensitivity profiles can be separated with this technique. Magn Reson Med 53:684–691, 2005.


Magnetic Resonance Materials in Physics Biology and Medicine | 1998

AUTO-SMASH: A self-calibrating technique for SMASH imaging

Peter M. Jakob; Mark A. Griswold; Robert R. Edelman; Daniel K. Sodickson

Recently a new fast magnetic resonance imaging strategy, SMASH, has been described, which is based on partially parallel imaging with radiofrequency coil arrays. In this paper, an internal sensitivity calibration technique for the SMASH imaging method using self-calibration signals is described. Coil sensitivity information required for SMASH imaging is obtained during the actual scan using correlations between undersampled SMASH signal data and additionally sampled calibration signals with appropriate offsets ink-space. The advantages of this sensitivity reference method are that no extra coil array sensitivity maps have to be acquired and that it provides coil sensitivity information in areas of highly non-uniform spin-density. This auto-calibrating approach can be easily implemented with only a small sacrifice of the overall time savings afforded by SMASH imaging. The results obtained from phantom imaging experiments and from cardiac studies in nine volunteers indicate that the self-calibrating approach is an effective method to increase the potential and the flexibility of rapid imaging with SMASH.


Magnetic Resonance in Medicine | 2001

VD-AUTO-SMASH imaging.

Robin M. Heidemann; Mark A. Griswold; Axel Haase; Peter M. Jakob

Recently a self‐calibrating SMASH technique, AUTO‐SMASH, was described. This technique is based on PPA with RF coil arrays using auto‐calibration signals. In AUTO‐SMASH, important coil sensitivity information required for successful SMASH reconstruction is obtained during the actual scan using the correlation between undersampled SMASH signal data and additionally sampled calibration signals with appropriate offsets in k‐space. However, AUTO‐SMASH is susceptible to noise in the acquired data and to imperfect spatial harmonic generation in the underlying coil array. In this work, a new modified type of internal sensitivity calibration, VD‐AUTO‐SMASH, is proposed. This method uses a VD k‐space sampling approach and shows the ability to improve the image quality without significantly increasing the total scan time. This new k‐space adapted calibration approach is based on a k‐space–dependent density function. In this scheme, fully sampled low‐spatial frequency data are acquired up to a given cutoff‐spatial frequency. Above this frequency, only sparse SMASH‐type sampling is performed. On top of the VD approach, advanced fitting routines, which allow an improved extraction of coil‐weighting factors in the presence of noise, are proposed. It is shown in simulations and in vivo cardiac images that the VD approach significantly increases the potential and flexibility of rapid imaging with AUTO‐SMASH. Magn Reson Med 45:1066–1074, 2001.


Magnetic Resonance in Medicine | 2005

Dynamic autocalibrated parallel imaging using temporal GRAPPA (TGRAPPA).

Felix A. Breuer; Peter Kellman; Mark A. Griswold; Peter M. Jakob

Current parallel imaging techniques for accelerated imaging require a fully encoded reference data set to estimate the spatial coil sensitivity information needed for reconstruction. In dynamic parallel imaging a time‐interleaved acquisition scheme can be used, which eliminates the need for separately acquiring additional reference data, since the signal from directly adjacent time frames can be merged to build a set of fully encoded full‐resolution reference data for coil calibration. In this work, we demonstrate that a time‐interleaved sampling scheme, in combination with autocalibrated GRAPPA (referred to as TGRAPPA), allows one to easily update the coil weights for the GRAPPA algorithm dynamically, thereby improving the acquisition efficiency. This method may update coil sensitivity estimates frame by frame, thereby tracking changes in relative coil sensitivities that may occur during the data acquisition. Magn Reson Med 53:981–985, 2005. Published 2005 Wiley‐Liss, Inc.


Magnetic Resonance in Medicine | 2004

Inversion recovery TrueFISP: Quantification of T1, T2, and spin density

Peter Schmitt; Mark A. Griswold; Peter M. Jakob; Markus Kotas; Vikas Gulani; Michael Flentje; Axel Haase

A novel procedure is proposed to extract T1, T2, and relative spin density from the signal time course sampled with a series of TrueFISP images after spin inversion. Generally, the recovery of the magnetization during continuous TrueFISP imaging can be described in good approximation by a three parameter monoexponential function S(t) = Sstst(1‐INV exp(‐t/T  *1 ). This apparent relaxation time T  *1 ≤ T1 depends on the flip angle as well as on both T1 and T2. Here, it is shown that the ratio T1/T2 can be directly extracted from the inversion factor INV, which describes the relation of the signal value extrapolated to t = 0 and the steady‐state signal. Analytical expressions are given for the derivation of T1, T2, and relative spin density directly from the fit parameters. Phantom results show excellent agreement with single point reference measurements. In human volunteers T1, T2, and spin density maps in agreement with literature values were obtained. Magn Reson Med 51:661–667, 2004.


Magnetic Resonance in Medicine | 2012

Ultrashort echo time imaging using pointwise encoding time reduction with radial acquisition (PETRA).

David Grodzki; Peter M. Jakob; Bjoern Heismann

Sequences with ultrashort echo times enable new applications of MRI, including bone, tendon, ligament, and dental imaging. In this article, a sequence is presented that achieves the shortest possible encoding time for each k‐space point, limited by pulse length, hardware switching times, and gradient performance of the scanner. In pointwise encoding time reduction with radial acquisition (PETRA), outer k‐space is filled with radial half‐projections, whereas the centre is measured single pointwise on a Cartesian trajectory. This hybrid sequence combines the features of single point imaging with radial projection imaging. No hardware changes are required. Using this method, 3D images with an isotropic resolution of 1 mm can be obtained in less than 3 minutes. The differences between PETRA and the ultrashort echo time (UTE) sequence are evaluated by simulation and phantom measurements. Advantages of pointwise encoding time reduction with radial acquisition are shown for tissue with a T2 below 1 ms. The signal to noise ratio and Contrast‐to‐noise ratio (CNR) performance, as well as possible limitations of the approach, are investigated. In‐vivo head, knee, ankle, and wrist examples are presented to prove the feasibility of the sequence. In summary, fast imaging with ultrashort echo time is enabled by PETRA and may help to establish new routine clinical applications of ultrashort echo time sequences. Magn Reson Med, 2012.


Magnetic Resonance in Medicine | 2006

Controlled Aliasing in Volumetric Parallel Imaging (2D CAIPIRINHA)

Felix A. Breuer; Martin Blaimer; Matthias F. Mueller; Nicole Seiberlich; Robin M. Heidemann; Mark A. Griswold; Peter M. Jakob

The CAIPIRINHA (Controlled Aliasing In Parallel Imaging Results IN Higher Acceleration) concept in parallel imaging has recently been introduced, which modifies the appearance of aliasing artifacts during data acquisition in order to improve the subsequent parallel imaging reconstruction procedure. This concept has been successfully applied to simultaneous multi‐slice imaging (MS CAIPIRINHA). In this work, we demonstrate that the concept of CAIPIRINHA can also be transferred to 3D imaging, where data reduction can be performed in two spatial dimensions simultaneously. In MS CAIPIRINHA, aliasing is controlled by providing individual slices with different phase cycles by means of alternating multi‐band radio frequency (RF) pulses. In contrast to MS CAIPIRINHA, 2D CAIPIRINHA does not require special RF pulses. Instead, aliasing in 2D parallel imaging can be controlled by modifying the phase encoding sampling strategy. This is done by shifting sampling positions from their normal positions in the undersampled 2D phase encoding scheme. Using this modified sampling strategy, coil sensitivity variations can be exploited more efficiently in multiple dimensions, resulting in a more robust parallel imaging reconstruction. Magn Reson Med, 2006.

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Thomas Kampf

University of Würzburg

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