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1

Koh, D. M., and H. C. Thoeny, eds. Diffusion-Weighted MR Imaging. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-78576-7.

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2

Moritani, Toshio, Sven Ekholm, and Per-Lennart Westesson. Diffusion-Weighted MR Imaging of the Brain. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-78785-3.

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3

Moritani, Toshio, and Aristides A. Capizzano, eds. Diffusion-Weighted MR Imaging of the Brain, Head and Neck, and Spine. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-62120-9.

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4

Clinical MR neuroimaging: Physiological and functional techniques. 2nd ed. New York: Cambridge University Press, 2010.

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5

Moritani, T., S. Ekholm, and P. L. Westesson. Diffusion-Weighted MR Imaging of the Brain. Springer, 2005.

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6

Moritani, Toshio, Sven Ekholm, and Per-Lennart A. Westesson. Diffusion-Weighted MR Imaging of the Brain. Springer, 2010.

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7

P. -L Westesson,T. Moritani,S. Ekholm. Diffusion-Weighted MR Imaging of the Brain. Springer, 2009.

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8

P. -L Westesson,T. Moritani,S. Ekholm. Diffusion-Weighted MR Imaging of the Brain. Springer, 2008.

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9

Moritani, T., S. Ekholm, and P. L. Westesson. Diffusion-Weighted MR Imaging of the Brain. Springer London, Limited, 2005.

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10

Diffusion-Weighted MR Imaging of the Brain. Berlin/Heidelberg: Springer-Verlag, 2005. http://dx.doi.org/10.1007/b137507.

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11

Moritani, Toshio, Sven Ekholm, and Per-Lennart A. Westesson. Diffusion-Weighted MR Imaging of the Brain. Springer London, Limited, 2009.

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12

Diffusion-Weighted MR Imaging of the Brain. Springer, 2009.

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13

Diffusion-Weighted MR Imaging of the Brain. Springer, 2004.

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14

Thoeny, Harriet C., and Dow-Mu Koh. Diffusion-Weighted MR Imaging: Applications in the Body. Springer, 2012.

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15

Clinical Applications of MR Diffusion and Perfusion Imaging Magnetic Resonance Imaging Clinics. W.B. Saunders Company, 2009.

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16

Diffusion-Weighted MR Imaging: Applications in the Body (Medical Radiology). Springer, 2010.

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17

Clinical MR Neuroimaging: Diffusion, Perfusion and Spectroscopy. Cambridge University Press, 2004.

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18

1964-, Gillard Jonathan H., Waldman Adam D. 1959-, and Barker Peter B. 1959-, eds. Clinical MR neuroimaging: Diffusion, perfusion, and spectroscopy. Cambridge: Cambridge University Press, 2005.

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19

1964-, Gillard Jonathan H., Waldman Adam D. 1959-, and Barker Peter B. 1959-, eds. Clinical MR neuroimaging: Diffusion, perfusion, and spectroscopy. Cambridge: Cambridge University Press, 2005.

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20

R. Nuri, M.d. Sener. MRI of the Pediatric Brain: Uncommon Disorders, Proton Mr Spectroscopy, Diffusion MRI. Warren H. Green, 2003.

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21

Capizzano, Aristides A., and Toshio Moritani. Diffusion Weighted MR Imaging of the Brain, Head and Neck, and Spine. Springer International Publishing AG, 2021.

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22

Capizzano, Aristides A., and Toshio Moritani. Diffusion-Weighted MR Imaging of the Brain, Head and Neck, and Spine. Springer International Publishing AG, 2022.

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23

Glockner, James F., Kazuhiro Kitajima, and Akira Kawashima. Magnetic resonance imaging. Edited by Christopher G. Winearls. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0015_update_001.

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Abstract:
Magnetic resonance imaging (MRI) provides excellent anatomic detail and soft tissue contrast for the evaluation of patients with renal disease. MRI needs longer scan time than computed tomography (CT); however, no radiation is involved. Gadolinium-based contrast agents (GBCAs) are used to help provide additional image contrast during MRI. MRI is indicated for characterization of renal mass, staging of malignant renal neoplasms, and determination of vena cava involvement by the renal tumour. Magnetic resonance (MR) angiography is widely accepted as a non-invasive imaging work-up of renal artery stenosis. MR urography is an alternative to CT urography to assess the upper urinary tract but does not identify urinary calculi. Diffusion-weighted imaging is a functional MR technique being used to characterize parenchymal renal disease and renal tumours. Nephrogenic systemic fibrosis is a rare but debilitating and potentially life-threatening condition which has been linked to exposure of GBCAs in patients with severe renal insufficiency. The risk versus benefit must be assessed before proceeding.
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24

Krause-Utz, Annegret, Inga Niedtfeld, Julia Knauber, and Christian Schmahl. Neurobiology of Borderline Personality Disorder. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199997510.003.0006.

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In this chapter, neuroimaging findings in BPD are discussed referring to the three core domains of BPD psychopathology: disturbed emotion processing and emotion dysregulation (including dissociation and altered pain processing), behavioral dysregulation and impulsivity, and interpersonal disturbances. Experimental approaches investigating BPD psychopathology on the subjective, behavioral, and neurobiological levels have become increasingly important for an improved understanding of BPD. Over the past decades, neuroimaging has become one of the most important tools in clinical neurobiology. Neuroimaging includes a broad spectrum of methods such as positron emission tomography (PET), structural and functional magnetic resonance imaging (fMRI), MR spectroscopy, and diffusion tensor imaging (DTI).
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