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Singleton Department of Radiology, Texas Children\u2019s Hospital and Baylor College of Medicine, Houston, TX, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yushin","family":"Takemoto","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Kumamoto University Hospital, Kumamoto, Kumamoto, Japan"},{"name":"Department of Neurosurgery, Japanese Red Cross Kumamoto Hospital, Kumamoto, Kumamoto, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kentaro","family":"Mori","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Yokohama Sakae Kyosai Hospital, Yokohama, Kanagawa, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tze Phei","family":"Kee","sequence":"additional","affiliation":[{"name":"Department of Neuroradiology, National Neuroscience Institute, Singapore"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"3804","reference":[{"key":"1","doi-asserted-by":"crossref","unstructured":"1) Iliff JJ, Wang M, Liao Y, et al. A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid <i>\u03b2<\/i>. <i>Sci Transl Med<\/i> 2012; 4: 147ra111.","DOI":"10.1126\/scitranslmed.3003748"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2) Iliff JJ, Wang M, Zeppenfeld DM, et al. Cerebral arterial pulsation drives paravascular CSF\u2013interstitial fluid exchange in the murine brain. <i>J Neurosci<\/i> 2013; 33: 18190\u201318199.","DOI":"10.1523\/JNEUROSCI.1592-13.2013"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3) Iliff JJ, Lee H, Yu M, et al. Brain-wide pathway for waste clearance captured by contrast-enhanced MRI. <i>J Clin Invest<\/i> 2013; 123: 1299\u20131309.","DOI":"10.1172\/JCI67677"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4) Xie L, Kang H, Xu Q, et al. Sleep drives metabolite clearance from the adult brain. <i>Science<\/i> 2013; 342: 373\u2013377.","DOI":"10.1126\/science.1241224"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5) Nedergaard M. Neuroscience. Garbage truck of the brain. <i>Science<\/i> 2013; 340: 1529\u20131530.","DOI":"10.1126\/science.1240514"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6) Silva I, Silva J, Ferreira R, et al. Glymphatic system, AQP4, and their implications in Alzheimer\u2019s disease. <i>Neurol Res Pract<\/i> 2021; 3: 5.","DOI":"10.1186\/s42466-021-00102-7"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7) Klostranec JM, Vucevic D, Bhatia KD, et al. Current concepts in intracranial interstitial fluid transport and the glymphatic system: part I\u2014anatomy and physiology. <i>Radiology<\/i> 2021; 301: 502\u2013514.","DOI":"10.1148\/radiol.2021202043"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8) Rasmussen MK, Mestre H, Nedergaard M: The glymphatic pathway in neurological disorders. <i>Lancet Neurol<\/i> 2018; 17: 1016\u20131024.","DOI":"10.1016\/S1474-4422(18)30318-1"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9) Al Masri M, Corell A, Micha\u00eblsson I, et al. The glymphatic system for neurosurgeons: a scoping review. <i>Neurosurg Rev<\/i> 2024; 47: 61.","DOI":"10.1007\/s10143-024-02291-6"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10) Hladky SB, Barrand MA. Mechanisms of fluid movement into, through and out of the brain: evaluation of the evidence. <i>Fluids Barriers CNS<\/i> 2014; 11: 26.","DOI":"10.1186\/2045-8118-11-26"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11) Kimelberg HK. Water homeostasis in the brain: basic concepts. <i>Neuroscience<\/i> 2004; 129: 851\u2013860.","DOI":"10.1016\/j.neuroscience.2004.07.033"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12) Klostranec JM, Vucevic D, Bhatia KD, et al. Current concepts in intracranial interstitial fluid transport and the glymphatic system: part II\u2014imaging techniques and clinical applications. <i>Radiology<\/i> 2021; 301: 516\u2013532.","DOI":"10.1148\/radiol.2021204088"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13) Louveau A, Herz J, Alme MN, et al. CNS lymphatic drainage and neuroinflammation are regulated by meningeal lymphatic vasculature. <i>Nat Neurosci<\/i> 2018; 21: 1380\u20131391.","DOI":"10.1038\/s41593-018-0227-9"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14) Sweeney MD, Zlokovic BV. A lymphatic waste-disposal system implicated in Alzheimer\u2019s disease. <i>Nature<\/i> 2018; 560: 172\u2013174.","DOI":"10.1038\/d41586-018-05763-0"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15) Abbott NJ, Pizzo ME, Preston JE, et al. The role of brain barriers in fluid movement in the CNS: is there a \u2018glymphatic\u2019 system? <i>Acta Neuropathol<\/i> 2018; 135: 387\u2013407.","DOI":"10.1007\/s00401-018-1812-4"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16) Mathiisen TM, Lehre KP, Danbolt NC, et al. The perivascular astroglial sheath provides a complete covering of the brain microvessels: an electron microscopic 3D reconstruction. <i>Glia<\/i> 2010; 58: 1094\u20131103.","DOI":"10.1002\/glia.20990"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17) Kiviniemi V, Wang X, Korhonen V, et al. Ultra-fast magnetic resonance encephalography of physiological brain activity\u2014glymphatic pulsation mechanisms? <i>J Cereb Blood Flow Metab<\/i> 2016; 36: 1033\u20131045.","DOI":"10.1177\/0271678X15622047"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18) Ahn JH, Cho H, Kim JH, et al. Meningeal lymphatic vessels at the skull base drain cerebrospinal fluid. <i>Nature<\/i> 2019; 572: 62\u201366.","DOI":"10.1038\/s41586-019-1419-5"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19) Wang DJ, Hua J, Cao D, et al. Neurofluids and the glymphatic system: anatomy, physiology, and imaging. <i>Br J Radiol<\/i> 2023; 96: 20230016.","DOI":"10.1259\/bjr.20230016"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20) Taoka T, Ito R, Nakamichi R, et al. Diffusion tensor image analysis along the perivascular space (DTI-ALPS): revisiting the meaning and significance of the method. <i>Magn Reson Med Sci<\/i> 2024; 23: 268\u2013290.","DOI":"10.2463\/mrms.rev.2023-0175"},{"key":"21","doi-asserted-by":"crossref","unstructured":"21) Kim J, Lee DA, Lee HJ, et al. Glymphatic system dysfunction in patients with occipital lobe epilepsy. <i>J Neuroimaging<\/i> 2023; 33: 455\u2013461.","DOI":"10.1111\/jon.13083"},{"key":"22","doi-asserted-by":"crossref","unstructured":"22) Schartz D, Finkelstein A, Hoang N, et al. Diffusion-weighted imaging reveals impaired glymphatic clearance in idiopathic intracranial hypertension. <i>AJNR Am J Neuroradiol<\/i> 2024; 45: 149\u2013154.","DOI":"10.3174\/ajnr.A8088"},{"key":"23","doi-asserted-by":"crossref","unstructured":"23) Macdonald RL. Delayed neurological deterioration after subarachnoid haemorrhage. <i>Nat Rev Neurol<\/i> 2014; 10: 44\u201358.","DOI":"10.1038\/nrneurol.2013.246"},{"key":"24","doi-asserted-by":"crossref","unstructured":"24) Liu E, Peng X, Ma H, et al. The involvement of aquaporin-4 in the interstitial fluid drainage impairment following subarachnoid hemorrhage. <i>Front Aging Neurosci<\/i> 2021; 12: 611494.","DOI":"10.3389\/fnagi.2020.611494"},{"key":"25","doi-asserted-by":"crossref","unstructured":"25) Wang J, Lv T, Jia F, et al. Subarachnoid hemorrhage distinctively disrupts the glymphatic and meningeal lymphatic systems in beagles. <i>Theranostics<\/i> 2024; 14: 6053\u20136070.","DOI":"10.7150\/thno.100982"},{"key":"26","doi-asserted-by":"crossref","unstructured":"26) Hou C, Li J, Wang B, et al. Dynamic evolution of the glymphatic system at the early stages of subarachnoid hemorrhage. <i>Front Neurol<\/i> 2022; 13: 924080.","DOI":"10.3389\/fneur.2022.924080"},{"key":"27","doi-asserted-by":"crossref","unstructured":"27) Yu Q, Wang H, Zhang W, et al. MRI-visible enlarged perivascular spaces in basal ganglia rather than centrum semiovale was associated with aneurysmal subarachnoid hemorrhage. <i>Front Neurol<\/i> 2024; 15: 1341499.","DOI":"10.3389\/fneur.2024.1341499"},{"key":"28","doi-asserted-by":"crossref","unstructured":"28) Li R, Zhao M, Yao D, et al. The role of the astrocyte in subarachnoid hemorrhage and its therapeutic implications. <i>Front Immunol<\/i> 2022; 13: 1008795.","DOI":"10.3389\/fimmu.2022.1008795"},{"key":"29","doi-asserted-by":"crossref","unstructured":"29) Goulay R, Flament J, Gauberti M, et al. Subarachnoid hemorrhage severely impairs brain parenchymal cerebrospinal fluid circulation in nonhuman primates. <i>Stroke<\/i> 2017; 48: 2301\u20132305.","DOI":"10.1161\/STROKEAHA.117.017014"},{"key":"30","doi-asserted-by":"crossref","unstructured":"30) Emmert AS, Iwasawa E, Shula C, et al. Impaired neural differentiation and glymphatic CSF flow in the <i>Ccdc39<\/i> rat model of neonatal hydrocephalus: genetic interaction with <i>L1cam<\/i>. <i>Dis Model Mech<\/i> 2019; 12: dmm040972.","DOI":"10.1242\/dmm.040972"},{"key":"31","doi-asserted-by":"crossref","unstructured":"31) Charidimou A, Boulouis G, Pasi M, et al. MRI-visible perivascular spaces in cerebral amyloid angiopathy and hypertensive arteriopathy. <i>Neurology<\/i> 2017; 88: 1157\u20131164.","DOI":"10.1212\/WNL.0000000000003746"},{"key":"32","doi-asserted-by":"crossref","unstructured":"32) Kim J, Joo B, Kim JW, et al. Aggravation of enlarged perivascular spaces in the centrum semiovale of patients with aneurysmal subarachnoid hemorrhage. <i>Clin Neuroradiol<\/i> 2022; 32: 79\u201387.","DOI":"10.1007\/s00062-021-01098-y"},{"key":"33","doi-asserted-by":"crossref","unstructured":"33) Hou C, Liu Q, Zhang H, et al. Nimodipine attenuates early brain injury by protecting the glymphatic system after subarachnoid hemorrhage in mice. <i>Neurochem Res<\/i> 2022; 47: 701\u2013712.","DOI":"10.1007\/s11064-021-03478-9"},{"key":"34","doi-asserted-by":"crossref","unstructured":"34) Golanov EV, Bovshik EI, Wong KK, et al. Subarachnoid hemorrhage-induced block of cerebrospinal fluid flow: role of brain coagulation factor III (tissue factor). <i>J Cereb Blood Flow Metab<\/i> 2018; 38: 793\u2013808.","DOI":"10.1177\/0271678X17701157"},{"key":"35","doi-asserted-by":"crossref","unstructured":"35) Tan X, Li X, Li R, et al. <i>\u03b2<\/i>-hydroxybutyrate alleviates neurological deficits by restoring glymphatic and inflammation after subarachnoid hemorrhage in mice. <i>Exp Neurol<\/i> 2024; 378: 114819.","DOI":"10.1016\/j.expneurol.2024.114819"},{"key":"36","doi-asserted-by":"crossref","unstructured":"36) Goyal N, Kumar P. Putting \u2018CSF\u2013shift edema\u2019 hypothesis to test: comparing cisternal and parenchymal pressures after basal cisternostomy for head injury. <i>World Neurosurg<\/i> 2021; 148: e252\u2013e263.","DOI":"10.1016\/j.wneu.2020.12.133"},{"key":"37","doi-asserted-by":"crossref","unstructured":"37) Shaia JK, Sharma N, Kumar M, et al. Changes in prevalence of idiopathic intracranial hypertension in the United States between 2015 and 2022, stratified by sex, race, and ethnicity. <i>Neurology<\/i> 2024; 102: e208036.","DOI":"10.1212\/WNL.0000000000208036"},{"key":"38","unstructured":"38) Colman BD, Boonstra F, Nguyen MNL, et al. Understanding the pathophysiology of idiopathic intracranial hypertension (IIH): a review of recent developments. <i>J Neurol Neurosurg Psychiatry<\/i> 2024; 95: 375\u2013383."},{"key":"39","doi-asserted-by":"crossref","unstructured":"39) Eide PK, Eidsvaag VA, Nagelhus EA, et al. Cortical astrogliosis and increased perivascular aquaporin-4 in idiopathic intracranial hypertension. <i>Brain Res<\/i> 2016; 1644: 161\u2013175.","DOI":"10.1016\/j.brainres.2016.05.024"},{"key":"40","doi-asserted-by":"crossref","unstructured":"40) Lenck S, Radovanovic I, Nicholson P, et al. Idiopathic intracranial hypertension: the veno-glymphatic connections. <i>Neurology<\/i> 2018; 91: 515\u2013522.","DOI":"10.1212\/WNL.0000000000006166"},{"key":"41","doi-asserted-by":"crossref","unstructured":"41) Jones O, Cutsforth-Gregory J, Chen J, et al. Idiopathic intracranial hypertension is associated with a higher burden of visible cerebral perivascular spaces: the glymphatic connection. <i>AJNR Am J Neuroradiol<\/i> 2021; 42: 2160\u20132164.","DOI":"10.3174\/ajnr.A7326"},{"key":"42","doi-asserted-by":"crossref","unstructured":"42) Schartz D, Finkelstein A, Bender M, et al. Association of extent of transverse sinus stenosis with cerebral glymphatic clearance in patients with idiopathic intracranial hypertension. <i>Neurology<\/i> 2024; 103: e209529.","DOI":"10.1212\/WNL.0000000000209529"},{"key":"43","doi-asserted-by":"crossref","unstructured":"43) Riggeal BD, Bruce BB, Saindane AM, et al. Clinical course of idiopathic intracranial hypertension with transverse sinus stenosis. <i>Neurology<\/i> 2013; 80: 289\u2013295.","DOI":"10.1212\/WNL.0b013e31827debd6"},{"key":"44","doi-asserted-by":"crossref","unstructured":"44) Abbott S, Chan F, Tahrani AA, et al. Weight management interventions for adults with idiopathic intracranial hypertension: a systematic review and practice recommendations. <i>Neurology<\/i> 2023; 101: e2138\u2013e2150.","DOI":"10.1212\/WNL.0000000000207866"},{"key":"45","doi-asserted-by":"crossref","unstructured":"45) Khatkar P, Hubbard JC, Hill L, et al. Experimental drugs for the treatment of idiopathic intracranial hypertension (IIH): shedding light on phase I and II trials. <i>Expert Opin Investig Drugs<\/i> 2023; 32: 1123\u20131131.","DOI":"10.1080\/13543784.2023.2288073"},{"key":"46","doi-asserted-by":"crossref","unstructured":"46) Salih M, Enriquez-Marulanda A, Khorasanizadeh M, et al. Cerebrospinal fluid shunting for idiopathic intracranial hypertension: a systematic review, meta-analysis, and implications for a modern management protocol. <i>Neurosurgery<\/i> 2022; 91: 529\u2013540.","DOI":"10.1227\/neu.0000000000002086"},{"key":"47","doi-asserted-by":"crossref","unstructured":"47) Prokop K, Op\u0119chowska A, Sie\u015bkiewicz A, et al. Effectiveness of optic nerve sheath fenestration in preserving vision in idiopathic intracranial hypertension: an updated meta-analysis and systematic review. <i>Acta Neurochir (Wien)<\/i> 2024; 166: 476.","DOI":"10.1007\/s00701-024-06345-y"},{"key":"48","doi-asserted-by":"crossref","unstructured":"48) Azzam AY, Mortezaei A, Morsy MM, et al. Venous sinus stenting for idiopathic intracranial hypertension: an updated meta-analysis. <i>J Neurol Sci<\/i> 2024; 459: 122948.","DOI":"10.1016\/j.jns.2024.122948"},{"key":"49","doi-asserted-by":"crossref","unstructured":"49) Lim J, Monteiro A, Kuo CC, et al. Stenting for venous sinus stenosis in patients with idiopathic intracranial hypertension: an updated systematic review and meta-analysis of the literature. <i>Neurosurgery<\/i> 2024; 94: 648\u2013656.","DOI":"10.1227\/neu.0000000000002718"},{"key":"50","unstructured":"50) Rohr A, D\u00f6rner L, Stingele R, et al. Reversibility of venous sinus obstruction in idiopathic intracranial hypertension. <i>AJNR Am J Neuroradiol<\/i> 2007; 28: 656\u2013659."},{"key":"51","doi-asserted-by":"crossref","unstructured":"51) AlRawili N, Al-Kuraishy HM, Al-Gareeb AI, et al. Trajectory of cardiogenic dementia: a new perspective. <i>J Cell Mol Med<\/i> 2025; 29: e70345.","DOI":"10.1111\/jcmm.70345"},{"key":"52","doi-asserted-by":"crossref","unstructured":"52) Sterling MR, Jannat-Khah D, Bryan J, et al. The prevalence of cognitive impairment among adults with incident heart failure: the \u201creasons for geographic and racial differences in stroke\u201d (REGARDS) study. <i>J Card Fail<\/i> 2019; 25: 130\u2013136.","DOI":"10.1016\/j.cardfail.2018.12.006"},{"key":"53","doi-asserted-by":"crossref","unstructured":"53) Xie W, Zheng F, Yan L, et al. Cognitive decline before and after incident coronary events. <i>J Am Coll Cardiol<\/i> 2019; 73: 3041\u20133050.","DOI":"10.1016\/j.jacc.2019.04.019"},{"key":"54","doi-asserted-by":"crossref","unstructured":"54) Yamada M, Ihara M, Okamoto Y, et al. The influence of chronic cerebral hypoperfusion on cognitive function and amyloid <i>\u03b2<\/i> metabolism in APP overexpressing mice. <i>PLoS One<\/i> 2011; 6: e16567.","DOI":"10.1371\/journal.pone.0016567"},{"key":"55","doi-asserted-by":"crossref","unstructured":"55) Carr JMJR, Hoiland RL, Fernandes IA, et al. Recent insights into mechanisms of hypoxia-induced vasodilatation in the human brain. <i>J Physiol<\/i> 2024; 602: 5601\u20135618.","DOI":"10.1113\/JP284608"},{"key":"56","doi-asserted-by":"crossref","unstructured":"56) Cheng Y, Chen B, Zhang M, et al. Carotid endarterectomy ameliorates cognitive impairment in clinical and experimental unilateral carotid artery stenosis. <i>J Am Heart Assoc<\/i> 2025; 14: e038388.","DOI":"10.1161\/JAHA.124.038388"},{"key":"57","doi-asserted-by":"crossref","unstructured":"57) Kress BT, Iliff JJ, Xia M, et al. Impairment of paravascular clearance pathways in the aging brain. <i>Ann Neurol<\/i> 2014; 76: 845\u2013861.","DOI":"10.1002\/ana.24271"},{"key":"58","doi-asserted-by":"crossref","unstructured":"58) Ang PS, Zhang DM, Azizi SA, et al. The glymphatic system and cerebral small vessel disease. <i>J Stroke Cerebrovasc Dis<\/i> 2024; 33: 107557.","DOI":"10.1016\/j.jstrokecerebrovasdis.2024.107557"},{"key":"59","doi-asserted-by":"crossref","unstructured":"59) Lee DH, Lee EC, Park SW, et al. Pathogenesis of cerebral small vessel disease: role of the glymphatic system dysfunction. <i>Int J Mol Sci<\/i> 2024; 25: 8752.","DOI":"10.3390\/ijms25168752"},{"key":"60","doi-asserted-by":"crossref","unstructured":"60) Ebinu JO, Matouk CC, Wallace MC, et al. Hydrocephalus secondary to hydrodynamic disequilibrium in an adult patient with a choroidal-type arteriovenous malformation. <i>Interv Neuroradiol<\/i> 2011; 17: 212\u2013216.","DOI":"10.1177\/159101991101700212"},{"key":"61","doi-asserted-by":"crossref","unstructured":"61) Alvarez H, Garcia Monaco R, Rodesch G, et al. Vein of galen aneurysmal malformations. <i>Neuroimaging Clin N Am<\/i> 2007; 17: 189\u2013206.","DOI":"10.1016\/j.nic.2007.02.005"},{"key":"62","doi-asserted-by":"crossref","unstructured":"62) W\u00e4lchli T, Bhatia KD, Guest W, et al. Identification of a T2-hyperintense perivascular space in brain arteriovenous malformations. <i>In Vivo<\/i> 2025; 39: 280\u2013291.","DOI":"10.21873\/invivo.13826"},{"key":"63","doi-asserted-by":"crossref","unstructured":"63) Brito A, Tsang ACO, Hilditch C, et al. Intracranial dural arteriovenous fistula as a reversible cause of dementia: case series and literature review. <i>World Neurosurg<\/i> 2019; 121: e543\u2013e553.","DOI":"10.1016\/j.wneu.2018.09.161"},{"key":"64","doi-asserted-by":"crossref","unstructured":"64) Itsekson-Hayosh Z, Carpani F, Mosimann PJ, et al. Dural arteriovenous fistulas: baseline cognitive changes and changes following treatment: a prospective longitudinal study. <i>AJNR Am J Neuroradiol<\/i> 2024; 45: 1878\u20131884.","DOI":"10.3174\/ajnr.A8449"},{"key":"65","doi-asserted-by":"crossref","unstructured":"65) Gramegna LL, Ortega G, Dinia L, et al. Cognitive improvement following endovascular embolization in patients with intracranial dural arteriovenous fistula: the Neuropsychology in dural Arterial Fistula (NAIF) study. <i>J Neurointerv Surg<\/i> 2025; 17: 87\u201393.","DOI":"10.1136\/jnis-2023-021033"},{"key":"66","doi-asserted-by":"crossref","unstructured":"66) Sanchez S, Wendt L, Hayakawa M, et al. Dural arteriovenous fistulas with cognitive impairment: angiographic characteristics and treatment outcomes. <i>Neurosurgery<\/i> 2024; 94: 1035\u20131043.","DOI":"10.1227\/neu.0000000000002802"}],"container-title":["Journal of Neuroendovascular Therapy"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/jnet\/19\/1\/19_ra.2025-0020\/_pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,6,21]],"date-time":"2025-06-21T00:43:23Z","timestamp":1750466603000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/jnet\/19\/1\/19_ra.2025-0020\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025]]},"references-count":66,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2025]]}},"URL":"https:\/\/doi.org\/10.5797\/jnet.ra.2025-0020","relation":{},"ISSN":["1882-4072","2186-2494"],"issn-type":[{"value":"1882-4072","type":"print"},{"value":"2186-2494","type":"electronic"}],"subject":[],"published":{"date-parts":[[2025]]},"article-number":"ra.2025-0020"}}