Abstract: In a method and a computer for identifying a group of persons, from a number of persons, to whom at least one contrast agent has been applied during an examination which was carried out in an imaging system with which medical images of each of the number of persons were produced, existing examination data provided for each of the number of persons are used to determine to which of those persons the at least one contrast agent was applied. The persons to whom at least one contrast agent was applied during the examination are identified as a group of persons. For each person in the group, person-specific contrast agent data are determined that include at least identification information identifying the person to whom the at least one contrast agent was applied, and contrast agent information identifying the fact that the at least one contrast agent was applied. A designation of each person in the group of persons is stored with that person's corresponding person-specific contrast agent data in a register.

Abstract: A simultaneous MR imaging method is described in which different types of atom are simultaneously excited and read out. First a multi-resonant RF excitation pulse is transmitted including a plurality of sub-signals assigned to different types of atom and having different frequency ranges. Simultaneously or in a synchronized manner, a gradient scheme common to the different types of atom is transmitted with which an unambiguous spatial assignment of received signals can be performed. In the subsequent readout process, an echo signal is received including different individual echoes of different types of atom. The received echo signal is separated into individual signals. Finally, image data is reconstructed from raw data obtained from the separated individual signals. Also described is an apparatus with which the above described method can be carried out.

Abstract: In a magnetic resonance method and apparatus to measure a sodium content in tissue in a first slice, a determination of a blood volume in blood vessels in the first slice is made, and an MR acquisition sequence to acquire MR data of a sodium-23 magnetization from the first slice is implemented. A signal proportion of the MR data that originates from the sodium-23 magnetization in blood vessels is calculated based on the determined blood volume in tissue. This signal proportion is subtracted from a total signal of the MR data to obtain a corrected signal that is proportional to the sodium content in tissue. The sodium content in tissue is calculated from the corrected signal.

Abstract: Waypoints for a steerable medical device are stored as the steerable medical device is moved within a patient. The stored waypoints are an ordered sequence of locations. The ordered sequence of locations defines a safe path within the patient for moving an articulatable portion of the steerable medical device. The articulatable portion of the steerable medical device is constrained to follow the safe path as the articulatable portion moves within the patient. For example, the articulatable portion of the steerable medical device is constrained to remain within a boundary region enclosing the safe path as the articulatable portion of the steerable medical device follows the safe path.

Abstract: A coil arrangement for a magnetic resonance tomography apparatus has plates that each contain at least one gradient coil.

Abstract: In a method for implementing an irreversible electroporation treatment with an electroporation device having at least two treatment electrodes, magnetic resonance exposures are acquired for visual monitoring of the treatment, and magnetic resonance-compatible electrodes are used as treatment electrodes. A magnetic resonance imaging apparatus has an electroporation device integrated therein, so as to be operable by co-use of at least some of the same components that arte used for image data acquisition.

Abstract: A method is disclosed for determination of positron-emission measurement information about a body area which is affected by at least one periodic movement process of an examination object during the course of positron-emission tomography. In at least one embodiment, the method includes a positron-emission measurement being carried out in the body area to be examined of the examination object in order to determine functional positron-emission measurement information, and recording, at the same time as the positron-emission measurement, anatomical measurement information about the body area to be examined is recorded, restricted to one recording plane, for at least one measurement time period, using an anatomical imaging method with high time resolution, in particular using a computed-tomography method.

Abstract: A coil arrangement for a magnetic resonance tomography apparatus has plates that each contain at least one gradient coil.

Abstract: Waypoints for a steerable medical device are stored as the steerable medical device is moved within a patient. The stored waypoints are an ordered sequence of locations. The ordered sequence of locations defines a safe path within the patient for moving an articulatable portion of the steerable medical device. The articulatable portion of the steerable medical device is constrained to follow the safe path as the articulatable portion moves within the patient. For example, the articulatable portion of the steerable medical device is constrained to remain within a boundary region enclosing the safe path as the articulatable portion of the steerable medical device follows the safe path.

Abstract: Waypoints for a steerable medical device are stored as the steerable medical device is moved within a patient. The stored waypoints are an ordered sequence of locations. The ordered sequence of locations defines a safe path within the patient for moving an articulatable portion of the steerable medical device. The articulatable portion of the steerable medical device is constrained to follow the safe path as the articulatable portion moves within the patient. For example, the articulatable portion of the steerable medical device is constrained to remain within a boundary region enclosing the safe path as the articulatable portion of the steerable medical device follows the safe path.

Abstract: A method is disclosed for determining positron emission measurement information in the context of positron emission tomography. The method includes carrying out a positron emission measurement, in a body area of a subject to be examined, to record positron emission measurement information with point resolution and determining a time frame of the measurement by, at the same time, generating images of the body area to be examined with a relatively higher time resolution and with point-resolved image data, using a second imaging method. Further, a local shift of points of individual images of the second imaging method is determined, caused by movement processes of the subject to be examined, and as a function thereof, of the positron emission measurement information for at least a part of the measurement period and of the body area to be examined. Finally, the positron emission measurement information is adjusted as a function of the determined shift.

Abstract: In a method for implementing an irreversible electroporation treatment with an electroporation device having at least two treatment electrodes, magnetic resonance exposures are acquired for visual monitoring of the treatment, and magnetic resonance-compatible electrodes are used as treatment electrodes. A magnetic resonance imaging apparatus has an electroporation device integrated therein, so as to be operable by co-use of at least some of the same components that arte used for image data acquisition.

Abstract: A combined PET/MRI tomography unit has a PET unit with a unit part assigned to the examination space, and a first evaluation unit for evaluating the PET electric signals. The unit part has a gamma ray detector. The combined unit has an MRI unit and a second evaluation unit for evaluating MRI signals. The MRI unit has a high frequency antenna as well as a gradient coil system, the high frequency antenna device being arranged nearer to the examination space than the gradient coil system, as well as a high frequency shield arranged between the gradient coil system and the high frequency antenna device. The PET unit part is arranged between the high frequency shield and the high frequency antenna device. A shielding cover for the high frequency antenna device faces the high frequency antenna device. The shielding cover is opaque to high frequency radiation.

Abstract: A sensor is disclosed for permitting detection of a substance in the body of a living being. In at least one embodiment, the sensor includes probe molecules, for binding the substance that is to be detected, and marking elements designed in such a way that the binding of the probe molecules to the substance to be detected is detectable by way of an imaging modality. For example, antigens or pathogens that are present only in a low concentration can be detected.

Abstract: A method for determining positron emission measurement information in the context of positron emission tomography is disclosed. The method includes using a marker substance to carry out a positron emission measurement, in a body area of a subject to be examined, to determine positron emission measurement information, and at the same time, generating images of the body area to be examined by way of a second medical method with a time resolution suitable for determining perfusion and/or diffusion information. The method further includes using the images from the second method to determine perfusion and/or diffusion information for at least a part of the measurement period, and evaluating the positron emission measurement information as a function of the perfusion and/or diffusion information.

Abstract: A nuclear-medical image is generated from a nuclear-medical data set that can be acquired with a dual modality tomography apparatus, which has both a scanner for acquisition of magnetic resonance images and a scanner for acquisition of nuclear-medical data sets within a common acquisition volume. A nuclear-medical data set and an MR image are thereby acquired, and a nuclear-medical magnetic resonance atlas is provided with a reference MR data set of the region of a reference patient to be imaged and a corresponding correction data set. A transformation that maps the reference MR data set to the MR image is generated and applied to the correction data set to generate a transformed correction data set that is registered with the nuclear-medical data set. The corrected nuclear-medical image is subsequently calculated from the transformed correction data set and the nuclear-medical data set.

Abstract: A positron emission tomography unit (PET), having a unit part assigned to an examination space and a first evaluation unit, is combined with a magnetic resonance tomography unit (MRT). The unit part of the PRT includes at least two gamma ray detector units with in each case an assigned electronics unit. The MRT includes a second evaluation unit, a gradient coil system and a high frequency antenna device formed as a stripline antenna device having at least two conductors. The high frequency antenna device is arranged nearer to the examination space than the gradient coil system with a high frequency shield between the gradient coil system and the high frequency antenna device. Each conductor of the stripline antenna device respectively includes a gamma ray detector unit with an assigned electronics unit.

Abstract: A method is disclosed for determination of positron-emission measurement information about a body area which is affected by at least one periodic movement process of an examination object during the course of positron-emission tomography. In at least one embodiment, the method includes a positron-emission measurement being carried out in the body area to be examined of the examination object in order to determine functional positron-emission measurement information, and recording, at the same time as the positron-emission measurement, anatomical measurement information about the body area to be examined is recorded, restricted to one recording plane, for at least one measurement time period, using an anatomical imaging method with high time resolution, in particular using a computed-tomography method.

Abstract: A method for determining positron emission measurement information in the context of positron emission tomography is disclosed. The method includes using a marker substance to carry out a positron emission measurement, in a body area of a subject to be examined, to determine positron emission measurement information, and at the same time, generating images of the body area to be examined by way of a second medical method with a time resolution suitable for determining perfusion and/or diffusion information. The method further includes using the images from the second method to determine perfusion and/or diffusion information for at least a part of the measurement period, and evaluating the positron emission measurement information as a function of the perfusion and/or diffusion information.

Abstract: A method is disclosed for determining positron emission measurement information in the context of positron emission tomography. The method includes carrying out a positron emission measurement, in a body area of a subject to be examined, to record positron emission measurement information with point resolution and determining a time frame of the measurement by, at the same time, generating images of the body area to be examined with a relatively higher time resolution and with point-resolved image data, using a second imaging method. Further, a local shift of points of individual images of the second imaging method is determined, caused by movement processes of the subject to be examined, and as a function thereof, of the positron emission measurement information for at least a part of the measurement period and of the body area to be examined. Finally, the positron emission measurement information is adjusted as a function of the determined shift.