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Schregel, Katharina
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Schregel, Katharina
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Schregel, Katharina
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Schregel, K.
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2018Journal Article [["dc.bibliographiccitation.firstpage","2283"],["dc.bibliographiccitation.issue","10"],["dc.bibliographiccitation.journal","Stroke"],["dc.bibliographiccitation.lastpage","2284"],["dc.bibliographiccitation.volume","49"],["dc.contributor.author","Psychogios, Marios-Nikos"],["dc.contributor.author","Schregel, Katharina"],["dc.date.accessioned","2020-12-10T18:38:08Z"],["dc.date.available","2020-12-10T18:38:08Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.1161/STROKEAHA.118.022148"],["dc.identifier.eissn","1524-4628"],["dc.identifier.issn","0039-2499"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/77194"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Relativity of Ischemic Core Volume Estimation"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2018Journal Article [["dc.bibliographiccitation.firstpage","362"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Journal of Stroke"],["dc.bibliographiccitation.lastpage","372"],["dc.bibliographiccitation.volume","20"],["dc.contributor.author","Schregel, Katharina"],["dc.contributor.author","Tsogkas, Ioannis"],["dc.contributor.author","Peter, Carolin"],["dc.contributor.author","Zapf, Antonia"],["dc.contributor.author","Behme, Daniel"],["dc.contributor.author","Schnieder, Marlena"],["dc.contributor.author","Maier, Ilko L."],["dc.contributor.author","Liman, Jan"],["dc.contributor.author","Knauth, Michael"],["dc.contributor.author","Psychogios, Marios-Nikos"],["dc.date.accessioned","2021-06-01T10:48:59Z"],["dc.date.available","2021-06-01T10:48:59Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.5853/jos.2018.00605"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/86121"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-425"],["dc.relation.eissn","2287-6405"],["dc.relation.issn","2287-6391"],["dc.title","Outcome Prediction Using Perfusion Parameters and Collateral Scores of Multi-Phase and Single-Phase CT Angiography in Acute Stroke: Need for One, Two, Three, or Thirty Scans?"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2019Journal Article [["dc.bibliographiccitation.firstpage","287"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","The Neuroradiology Journal"],["dc.bibliographiccitation.lastpage","293"],["dc.bibliographiccitation.volume","32"],["dc.contributor.author","Schnieder, M"],["dc.contributor.author","Psychogios, MN"],["dc.contributor.author","Maier, IL"],["dc.contributor.author","Tsogkas, I"],["dc.contributor.author","Schregel, K"],["dc.contributor.author","Kleinknecht, A"],["dc.contributor.author","Knauth, M"],["dc.contributor.author","Bähr, M."],["dc.contributor.author","Liman, Jan"],["dc.contributor.author","Behme, D"],["dc.date.accessioned","2020-12-10T18:38:38Z"],["dc.date.available","2020-12-10T18:38:38Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1177/1971400918791700"],["dc.identifier.eissn","2385-1996"],["dc.identifier.issn","1971-4009"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/77395"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","The problem of strict image-based inclusion criteria for mechanical thrombectomy – an analysis of stroke patients with an initial low CBV-ASPECTS score"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2017Journal Article [["dc.bibliographiccitation.firstpage","1253"],["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Journal of NeuroInterventional Surgery"],["dc.bibliographiccitation.lastpage","1257"],["dc.bibliographiccitation.volume","9"],["dc.contributor.author","Leyhe, Johanna Rosemarie"],["dc.contributor.author","Tsogkas, Ioannis"],["dc.contributor.author","Hesse, Amélie Carolina"],["dc.contributor.author","Behme, Daniel"],["dc.contributor.author","Schregel, Katharina"],["dc.contributor.author","Papageorgiou, Ismini"],["dc.contributor.author","Liman, Jan"],["dc.contributor.author","Knauth, Michael"],["dc.contributor.author","Psychogios, Marios-Nikos"],["dc.date.accessioned","2020-12-10T18:37:18Z"],["dc.date.available","2020-12-10T18:37:18Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1136/neurintsurg-2016-012866"],["dc.identifier.eissn","1759-8486"],["dc.identifier.issn","1759-8478"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/76904"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Latest generation of flat detector CT as a peri-interventional diagnostic tool: a comparative study with multidetector CT"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2020Journal Article [["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Cancer Imaging"],["dc.bibliographiccitation.volume","20"],["dc.contributor.author","Schregel, Katharina"],["dc.contributor.author","Nowicki, Michal O."],["dc.contributor.author","Palotai, Miklos"],["dc.contributor.author","Nazari, Navid"],["dc.contributor.author","Zane, Rachel"],["dc.contributor.author","Sinkus, Ralph"],["dc.contributor.author","Lawler, Sean E."],["dc.contributor.author","Patz, Samuel"],["dc.date.accessioned","2021-04-14T08:26:30Z"],["dc.date.available","2021-04-14T08:26:30Z"],["dc.date.issued","2020"],["dc.identifier.doi","10.1186/s40644-020-00314-1"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/81973"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","1470-7330"],["dc.title","Magnetic Resonance Elastography reveals effects of anti-angiogenic glioblastoma treatment on tumor stiffness and captures progression in an orthotopic mouse model"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2021Book Chapter [["dc.bibliographiccitation.firstpage","409"],["dc.bibliographiccitation.lastpage","415"],["dc.contributor.author","Schregel, Katharina"],["dc.contributor.author","Psychogios, Marios-Nikos"],["dc.date.accessioned","2021-06-02T10:44:31Z"],["dc.date.available","2021-06-02T10:44:31Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.1016/B978-0-444-64034-5.00022-5"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/87071"],["dc.notes.intern","DOI-Import GROB-425"],["dc.publisher","Elsevier"],["dc.relation.isbn","978-0-444-64034-5"],["dc.relation.ispartof","Interventional Neuroradiology"],["dc.title","Emerging stroke systems of care in Germany"],["dc.type","book_chapter"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2021Journal Article [["dc.bibliographiccitation.journal","Frontiers in Neuroscience"],["dc.bibliographiccitation.volume","15"],["dc.contributor.author","Schregel, Katharina"],["dc.contributor.author","Baufeld, Caroline"],["dc.contributor.author","Palotai, Miklos"],["dc.contributor.author","Meroni, Roberta"],["dc.contributor.author","Fiorina, Paolo"],["dc.contributor.author","Wuerfel, Jens"],["dc.contributor.author","Sinkus, Ralph"],["dc.contributor.author","Zhang, Yong-Zhi"],["dc.contributor.author","McDannold, Nathan"],["dc.contributor.author","Guttmann, Charles R. G."],["dc.date.accessioned","2021-07-05T14:57:55Z"],["dc.date.available","2021-07-05T14:57:55Z"],["dc.date.issued","2021"],["dc.description.abstract","Experimental autoimmune encephalomyelitis (EAE) is a model of multiple sclerosis (MS). EAE reflects important histopathological hallmarks, dissemination, and diversity of the disease, but has only moderate reproducibility of clinical and histopathological features. Focal lesions are less frequently observed in EAE than in MS, and can neither be constrained to specific locations nor timed to occur at a pre-specified moment. This renders difficult any experimental assessment of the pathogenesis of lesion evolution, including its inflammatory, degenerative (demyelination and axonal degeneration), and reparatory (remyelination, axonal sprouting, gliosis) component processes. We sought to develop a controlled model of inflammatory, focal brain lesions in EAE using focused ultrasound (FUS). We hypothesized that FUS induced focal blood brain barrier disruption (BBBD) will increase the likelihood of transmigration of effector cells and subsequent lesion occurrence at the sonicated location. Lesion development was monitored with conventional magnetic resonance imaging (MRI) as well as with magnetic resonance elastography (MRE) and further analyzed by histopathological means. EAE was induced in 12 6–8 weeks old female C57BL/6 mice using myelin oligodendrocyte glycoprotein (MOG) peptide. FUS-induced BBBD was performed 6, 7, and 9 days after immunization in subgroups of four animals and in an additional control group. MRI and MRE were performed on a 7T horizontal bore small animal MRI scanner. Imaging was conducted longitudinally 2 and 3 weeks after disease induction and 1 week after sonication in control animals, respectively. The scan protocol comprised contrast-enhanced T1-weighted and T2-weighted sequences as well as MRE with a vibration frequency of 1 kHz. Animals were sacrificed for histopathology after the last imaging time point. The overall clinical course of EAE was mild. A total of seven EAE animals presented with focal T2w hyperintense signal alterations in the sonicated hemisphere. These were most frequent in the group of animals sonicated 9 days after immunization. Histopathology revealed foci of activated microglia/macrophages in the sonicated right hemisphere of seven EAE animals. Larger cellular infiltrates or apparent demyelination were not seen. Control animals showed no abnormalities on MRI and did not have clusters of activated microglia/macrophages at the sites targeted with FUS. None of the animals had hemorrhages or gross tissue damage as potential side effects of FUS. EAE-animals tended to have lower values of viscoelasticity and elasticity in the sonicated compared to the contralateral parenchyma. This trend was significant when comparing the right sonicated to the left normal hemisphere and specifically the right sonicated compared to the left normal cortex in animals that underwent FUS-BBBD 9 days after immunization (right vs. left hemisphere: mean viscoelasticity 6.1 vs. 7.2 kPa; p = 0.003 and mean elasticity 4.9 vs. 5.7 kPa, p = 0.024; right vs. left cortex: mean viscoelasticity 5.8 vs. 7.5 kPa; p = 0.004 and mean elasticity 5 vs. 6.5 kPa; p = 0.008). A direct comparison of the biomechanical properties of focal T2w hyperintensities with normal appearing brain tissue did not yield significant results. Control animals showed no differences in viscoelasticity between sonicated and contralateral brain parenchyma. We here provide first evidence for a controlled lesion induction model in EAE using FUS-induced BBBD. The observed lesions in EAE are consistent with foci of activated microglia that may be interpreted as targeted initial inflammatory activity and which have been described as pre-active lesions in MS. Such foci can be identified and monitored with MRI. Moreover, the increased inflammatory activity in the sonicated brain parenchyma seems to have an effect on overall tissue matrix structure as reflected by changes of biomechanical parameters."],["dc.description.abstract","Experimental autoimmune encephalomyelitis (EAE) is a model of multiple sclerosis (MS). EAE reflects important histopathological hallmarks, dissemination, and diversity of the disease, but has only moderate reproducibility of clinical and histopathological features. Focal lesions are less frequently observed in EAE than in MS, and can neither be constrained to specific locations nor timed to occur at a pre-specified moment. This renders difficult any experimental assessment of the pathogenesis of lesion evolution, including its inflammatory, degenerative (demyelination and axonal degeneration), and reparatory (remyelination, axonal sprouting, gliosis) component processes. We sought to develop a controlled model of inflammatory, focal brain lesions in EAE using focused ultrasound (FUS). We hypothesized that FUS induced focal blood brain barrier disruption (BBBD) will increase the likelihood of transmigration of effector cells and subsequent lesion occurrence at the sonicated location. Lesion development was monitored with conventional magnetic resonance imaging (MRI) as well as with magnetic resonance elastography (MRE) and further analyzed by histopathological means. EAE was induced in 12 6–8 weeks old female C57BL/6 mice using myelin oligodendrocyte glycoprotein (MOG) peptide. FUS-induced BBBD was performed 6, 7, and 9 days after immunization in subgroups of four animals and in an additional control group. MRI and MRE were performed on a 7T horizontal bore small animal MRI scanner. Imaging was conducted longitudinally 2 and 3 weeks after disease induction and 1 week after sonication in control animals, respectively. The scan protocol comprised contrast-enhanced T1-weighted and T2-weighted sequences as well as MRE with a vibration frequency of 1 kHz. Animals were sacrificed for histopathology after the last imaging time point. The overall clinical course of EAE was mild. A total of seven EAE animals presented with focal T2w hyperintense signal alterations in the sonicated hemisphere. These were most frequent in the group of animals sonicated 9 days after immunization. Histopathology revealed foci of activated microglia/macrophages in the sonicated right hemisphere of seven EAE animals. Larger cellular infiltrates or apparent demyelination were not seen. Control animals showed no abnormalities on MRI and did not have clusters of activated microglia/macrophages at the sites targeted with FUS. None of the animals had hemorrhages or gross tissue damage as potential side effects of FUS. EAE-animals tended to have lower values of viscoelasticity and elasticity in the sonicated compared to the contralateral parenchyma. This trend was significant when comparing the right sonicated to the left normal hemisphere and specifically the right sonicated compared to the left normal cortex in animals that underwent FUS-BBBD 9 days after immunization (right vs. left hemisphere: mean viscoelasticity 6.1 vs. 7.2 kPa; p = 0.003 and mean elasticity 4.9 vs. 5.7 kPa, p = 0.024; right vs. left cortex: mean viscoelasticity 5.8 vs. 7.5 kPa; p = 0.004 and mean elasticity 5 vs. 6.5 kPa; p = 0.008). A direct comparison of the biomechanical properties of focal T2w hyperintensities with normal appearing brain tissue did not yield significant results. Control animals showed no differences in viscoelasticity between sonicated and contralateral brain parenchyma. We here provide first evidence for a controlled lesion induction model in EAE using FUS-induced BBBD. The observed lesions in EAE are consistent with foci of activated microglia that may be interpreted as targeted initial inflammatory activity and which have been described as pre-active lesions in MS. Such foci can be identified and monitored with MRI. Moreover, the increased inflammatory activity in the sonicated brain parenchyma seems to have an effect on overall tissue matrix structure as reflected by changes of biomechanical parameters."],["dc.identifier.doi","10.3389/fnins.2021.665722"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/87771"],["dc.notes.intern","DOI-Import GROB-441"],["dc.relation.eissn","1662-453X"],["dc.title","Targeted Blood Brain Barrier Opening With Focused Ultrasound Induces Focal Macrophage/Microglial Activation in Experimental Autoimmune Encephalomyelitis"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2017Journal Article [["dc.bibliographiccitation.firstpage","300"],["dc.bibliographiccitation.journal","Journal of the neurological sciences"],["dc.bibliographiccitation.lastpage","304"],["dc.bibliographiccitation.volume","372"],["dc.contributor.author","Maier, Ilko L."],["dc.contributor.author","Behme, Daniel"],["dc.contributor.author","Schnieder, Marlena"],["dc.contributor.author","Tsogkas, Ioannis"],["dc.contributor.author","Schregel, Katharina"],["dc.contributor.author","Kleinknecht, Alexander"],["dc.contributor.author","Wasser, Katrin"],["dc.contributor.author","Bähr, Mathias"],["dc.contributor.author","Knauth, Michael"],["dc.contributor.author","Psychogios, Marios"],["dc.contributor.author","Liman, Jan"],["dc.date.accessioned","2018-01-09T10:18:58Z"],["dc.date.available","2018-01-09T10:18:58Z"],["dc.date.issued","2017"],["dc.description.abstract","Although endovascular treatment for proximal cerebral vessel occlusion is very effective, it remains controversial if intravenous thrombolysis (IVT) prior to endovascular treatment is superior compared to endovascular treatment alone. In this study we compared functional outcomes and recanalization rates of endovascularly treated stroke patients with and without bridging IVT."],["dc.identifier.doi","10.1016/j.jns.2016.12.001"],["dc.identifier.pmid","28017233"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/11576"],["dc.language.iso","en"],["dc.notes.status","final"],["dc.relation.eissn","1878-5883"],["dc.title","Bridging-therapy with intravenous recombinant tissue plasminogen activator improves functional outcome in patients with endovascular treatment in acute stroke"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dspace.entity.type","Publication"]]Details DOI PMID PMC2020Journal Article [["dc.bibliographiccitation.firstpage","102109"],["dc.bibliographiccitation.journal","NeuroImage: Clinical"],["dc.bibliographiccitation.volume","25"],["dc.contributor.author","Bunevicius, Adomas"],["dc.contributor.author","Schregel, Katharina"],["dc.contributor.author","Sinkus, Ralph"],["dc.contributor.author","Golby, Alexandra"],["dc.contributor.author","Patz, Samuel"],["dc.date.accessioned","2020-12-10T15:20:31Z"],["dc.date.available","2020-12-10T15:20:31Z"],["dc.date.issued","2020"],["dc.identifier.doi","10.1016/j.nicl.2019.102109"],["dc.identifier.issn","2213-1582"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/72696"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","REVIEW: MR elastography of brain tumors"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2017Journal Article [["dc.bibliographiccitation.firstpage","3152"],["dc.bibliographiccitation.issue","11"],["dc.bibliographiccitation.journal","Stroke"],["dc.bibliographiccitation.lastpage","3155"],["dc.bibliographiccitation.volume","48"],["dc.contributor.author","Psychogios, Marios-Nikos"],["dc.contributor.author","Behme, Daniel"],["dc.contributor.author","Schregel, Katharina"],["dc.contributor.author","Tsogkas, Ioannis"],["dc.contributor.author","Maier, Ilko L."],["dc.contributor.author","Leyhe, Johanna Rosemarie"],["dc.contributor.author","Zapf, Antonia"],["dc.contributor.author","Tran, Julia"],["dc.contributor.author","Bähr, Mathias"],["dc.contributor.author","Knauth, Michael"],["dc.date.accessioned","2021-06-01T10:47:50Z"],["dc.date.available","2021-06-01T10:47:50Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1161/STROKEAHA.117.018077"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/85732"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-425"],["dc.relation.eissn","1524-4628"],["dc.relation.issn","0039-2499"],["dc.title","One-Stop Management of Acute Stroke Patients"],["dc.title.alternative","Minimizing Door-to-Reperfusion Times"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI