Dataset of voxelwise correlated signal values of ADC, rCBV and FAP-specific PET of 13 Glioblastoma patients
This dataset is based on multimodal MRI and FAP-specific PET/CT Imaging applied to 13 patients with histologically proven glioblastomas. Imaging Data was processed using Medical Imaging Interaction Toolkit (MITK) software. MRI images (contrast enhanced T1w, T2w/FLAIR, ADC, rCBV) were co-registrated...
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| Main Authors: | , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
August 2020
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| In: |
Data in Brief
Year: 2020, Volume: 31, Pages: 11-5 |
| ISSN: | 2352-3409 |
| DOI: | 10.1016/j.dib.2020.105712 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.dib.2020.105712 Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S2352340920306065 |
| Author Notes: | Manuel Röhrich, Lisa Loi, Ralf Floca, Uwe Haberkorn, Daniel Paech |
| Summary: | This dataset is based on multimodal MRI and FAP-specific PET/CT Imaging applied to 13 patients with histologically proven glioblastomas. Imaging Data was processed using Medical Imaging Interaction Toolkit (MITK) software. MRI images (contrast enhanced T1w, T2w/FLAIR, ADC, rCBV) were co-registrated with FAP-specific PET images. T2w/FLAIR hyperintensities and contrast enhancing lesions were segmented manually. Necrotic areas were segmented manually and subtracted from T2w/FLAIR hyperintensities and contrast enhancing lesions. Voxelwise ADC/rCBV and PET signal intensities in projection on T2w/FLAIR hyperintensities and contrast enhancing lesions were extracted using the pixel dumper function of the MITK software and stored as excel-files. The data presented in this article has been analysed and described in the article FAP-specific “PET signaling shows a moderately positive correlation with relative CBV and no correlation with ADC in 13 IDH wildtype Glioblastomas” published in the European Journal of Radiology. |
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| Item Description: | Gesehen am 21.07.2026 |
| Physical Description: | Online Resource |
| ISSN: | 2352-3409 |
| DOI: | 10.1016/j.dib.2020.105712 |