20 Chapter 1 54. Václavů L, Meynart BN, Mutsaerts HJMM, et al. Hemodynamic provocation with acetazolamide shows impaired cerebrovascular reserve in adults with sickle cell disease. Haematologica 2019; 104: 690–699. 55. Rodgers ZB, Detre JA, Wehrli FW. MRI-based methods for quantification of the cerebral metabolic rate of oxygen. Journal of Cerebral Blood Flow and Metabolism 2016; 36: 1165–1185. 56. Angleys H, Jespersen SN, Østergaard L. The effects of capillary transit time heterogeneity on the BOLD signal. Hum Brain Mapp 2018; 39: 2329–2352. 57. Fantini S, Sassaroli A, Tgavalekos KT, et al. Cerebral blood flow and autoregulation: current measurement techniques and prospects for noninvasive optical methods. Neurophotonics 2016; 3: 031411. 58. Murkin JM. Cerebral autoregulation: The role of CO2 in metabolic homeostasis. Semin Cardiothorac Vasc Anesth 2007; 11: 269–273. 59. Nagtegaal SHJ, David S, Snijders TJ, et al. Effect of radiation therapy on cerebral cortical thickness in glioma patients: Treatment-induced thinning of the healthy cortex. Neuro-Oncology Advances; 2. Epub ahead of print 2020. DOI: 10.1093/ noajnl/vdaa060. 60. Nagtegaal SHJ, David S, Philippens MEP, et al. Dose-dependent volume loss in subcortical deep grey matter structures after cranial radiotherapy. Clin Transl Radiat Oncol 2021; 26: 35–41. 61. Nagtegaal SHJ, David S, van Grinsven EE, et al. Morphological changes after cranial fractionated photon radiotherapy: Localized loss of white matter and grey matter volume with increasing dose. Clin Transl Radiat Oncol 2021; 31: 14–20. 62. Nazem-Zadeh MR, Chapman CH, Lawrence TL, et al. Radiation therapy effects on white matter fiber tracts of the limbic circuit. Med Phys 2012; 39: 5603–5613. 63. Zhu T, Chapman CH, Tsien C, et al. Effect of the Maximum Dose on White Matter Fiber Bundles Using Longitudinal Diffusion Tensor Imaging. Int J Radiat Oncol Biol Phys 2016; 96: 696–705. 64. Connor M, Karunamuni R, McDonald C, et al. Regional susceptibility to dosedependent white matter damage after brain radiotherapy. Radiotherapy and Oncology 2017; 123: 209–217. 65. Tibbs MD, Huynh-Le MP, Karunamuni R, et al. Microstructural Injury to LeftSided Perisylvian White Matter Predicts Language Decline After Brain Radiation Therapy. Int J Radiat Oncol Biol Phys 2020; 108: 1218–1228. 66. Chapman CH, Zhu T, Nazem-Zadeh M, et al. Diffusion tensor imaging predicts cognitive function change following partial brain radiotherapy for low-grade and benign tumors. Radiotherapy and Oncology 2016; 120: 234–240. 67. Chapman CH, Nagesh V, Sundgren PC, et al. Diffusion tensor imaging of normalappearing white matter as biomarker for radiation-induced late delayed cognitive decline. Int J Radiat Oncol Biol Phys 2012; 82: 2033–2040. 68. Huynh-Le MP, Tibbs MD, Karunamuni R, et al. Microstructural Injury to Corpus Callosum and Intrahemispheric White Matter Tracts Correlate With Attention and Processing Speed Decline After Brain Radiation. Int J Radiat Oncol Biol Phys 2021; 110: 337–347. 69. Jiang D, Lin Z, Liu P, et al. Brain Oxygen Extraction Is Differentially Altered by Alzheimer’s and Vascular Diseases. Journal of Magnetic Resonance Imaging 2020; 52: 1829–1837.
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