428 results on '"Gizewski, E"'
Search Results
152. Acute bleeding of a cavernous malformation of the conus medullaris
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Obermann, M, primary, Gizewski, E, additional, and Maschke, M, additional
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- 2005
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153. Aktivierung von aufmerksamkeitsassoziierten Strukturen bei MS-Patienten in Abhängigkeit von Aufmerksamkeitsdefiziten: eine fMRT-Studie
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Nebel, K, primary, Stude, P, additional, Wiese, H, additional, Seyfarth, J, additional, Gizewski, E, additional, Diener, H.C, additional, and Limmroth, V, additional
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- 2005
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154. Vergleichende fMRT-Studie zur zerebellären Aktivierung bei der Silbenwiederholung und dem Lesen von Substantiven
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Schorn, C.F, primary, Frings, M, additional, Dimitrova, A, additional, Elles, H.G, additional, Hein-Kropp, C, additional, Gizewski, E, additional, and Timmann, D, additional
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- 2005
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155. Stenting plus Coiling bei akut rupturierten intrakraniellen Aneurysmen
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Wanke, I, primary, Gizewski, E, additional, Dörfler, A, additional, Stolke, D, additional, and Forsting, M, additional
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- 2005
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156. Aktivierung des visuellen Kortex unter Alkoholeinfluss: eine fMRT-Studie
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Schlamann, M, primary, Gizewski, E, additional, deGreiff, A, additional, Grewe, K, additional, Freislederer, A, additional, and Forsting, M, additional
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- 2005
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157. Untersuchung der Gehirnaktivierung durch visuelle sexuelle Stimulation in heterosexuellen und homosexuellen Männern mittels funktioneller Magnetresonanztomographie
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Paul, T, primary, Schiffer, B, additional, Zwarg, T, additional, Krüger, T, additional, Karama, S, additional, Schedlowski, M, additional, Forsting, M, additional, and Gizewski, E, additional
- Published
- 2005
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158. Cerebellar agenesis II: Motor and language functions
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Richter, S., primary, Dimitrova, A., additional, Hein-Kropp, C., additional, Wilhelm, H., additional, Gizewski, E., additional, and Timmann, D., additional
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- 2005
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159. Pathophysiologie und Therapie des reversiblen posterioren Leukoenzephalopathiesyndroms (RPLS)
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Obermann, M., primary, Kastrup, O., additional, Gizewski, E., additional, and Maschke, M., additional
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- 2004
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160. Missing SMA Activation in Self-Initiated Movements after Chronic Prefrontal Traumatic Brain Injury: An Event-Related fMRI Study
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Wiese, H, primary, Toennes, C, additional, Nebel, K, additional, de Greiff, A, additional, Gizewski, E, additional, Forsting, M, additional, and Stude, P, additional
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- 2004
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161. Cerebellar mutism
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Ozimek, A., primary, Richter, S., additional, Hein–Kropp, C., additional, Schoch, B., additional, Gorißen, B., additional, Kaiser, O., additional, Gizewski, E., additional, Ziegler, W., additional, and Timmann, D., additional
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- 2004
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162. Isolierte und partiell reversible Leukoenzephalopathie bei Vitamin B12-Mangel
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Vry, MS, primary, Haerter, K, additional, Kastrup, O, additional, Gizewski, E, additional, Frings, M, additional, and Maschke, M, additional
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- 2004
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163. Akute isolierte hypertensive Leukencephalopathie des Hirnstamms
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Obermann, M, primary, Kastrup, O, additional, Busch, E, additional, Gizewski, E, additional, and Maschke, M, additional
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- 2004
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164. Cognitive sub-components in solving the tower of London test — An FMRI study in healthy volunteers and patients with schizophrenia
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Thienel, R., primary, Bender, S., additional, Mu¨ller, B.W., additional, Gizewski, E., additional, and Schall, U., additional
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- 2003
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165. Epidermoid oder Arachnoidalzyste: CISS, FLAIR und Diffusionsbilder als Ausweg aus dem diagnostischen Dilemma
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Gizewski, E. RM. R, primary
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- 2001
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166. Dose Management for X-Ray and CT: Systematic Comparison of Exposition Values from Two Institutes to Diagnostic Reference Levels and Use of Results for Optimisation of Exposition.
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Schäfer, S., Alejandre-Lafont, E., Schmidt, T., Gizewski, E. R., Fiebich, M., and Krombach, G. A.
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- 2014
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167. Application of Extracellular Gadolinium-based MRI Contrast Agents and the Risk of Nephrogenic Systemic Fibrosis.
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Heverhagen, J. T., Krombach, G. A., and Gizewski, E.
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- 2014
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168. Dual Energy CT Myelography after Lumbar Osteosynthesis.
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Grams, A. E., Sender, J., Moritz, R., Obert, M., Stein, M., Oertel, M., Krombach, G. A., Gizewski, E. R., and Schmidt, T.
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- 2014
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169. Do children with focal cerebellar lesions show deficits in shifting attention?
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Schoch, B., Gorissen, B., Richter, S., Ozimek, A., Kaiser, O., Dimitrova, A., Regel, J. P., Wieland, R., Hövel, M., Gizewski, E., and Timmann, D.
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CEREBELLAR cortex ,TUMORS ,MEDICAL imaging systems ,CHILDREN - Abstract
More recent findings suggest a possible role of the cerebellum in nonmotor functions. Disability of individuals with cerebellar damage in rapidly shifting attention is one frequently used example to support cerebellar involvement in mental skills. The original proposal was based on findings in five children with chronic surgical lesions of the cerebellum and a young adult with a degenerative disorder. The aim of the present study was to repeat Akshoomoff and Courchesne's initial findings in a larger group of children with focal cerebellar lesions. Ten children with cerebellar lesions and 10 age- and sex-matched controls were tested. Neocerebellar areas were affected in all children with cerebellar damage except one based on detailed analysis of MRI scans. Subjects had to perform a focus and a shift attention task. Two visual and two auditory stimuli were presented in a pseudorandom order. An ellipse and a high-pitched tone were presented less frequently than a circle and a low-pitched tone. Rare stimuli were presented at five different time intervals. In the focus tasks, subjects had to react to the same rare stimulus of one of the two modalities. In the shift task, subjects had to switch between the two rare stimuli. Motor deficits based on reaction times were small in cerebellar children compared with controls. The ability of target detection did not significantly differ in the children with cerebellar lesions compared with the control children in both the focus and the shift attention task. In particular, children with cerebellar damage showed no significant impairment in rapid (<2 s) shifts of attention. The present findings indicate that the cerebellum may be less critical in attention related processes than suggested previously. [ABSTRACT FROM AUTHOR]
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- 2004
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170. Cavernous malformation with hemorrhage of the conus medullaris and progressive sensory loss.
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Obermann, Mark, Gizewski, E. R., Felsberg, J., and Maschke, M.
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SPINAL cord abnormalities ,CONUS medullaris ,HEMORRHAGE ,SPINAL cord ,MAGNETIC resonance imaging - Abstract
Numerous studies have shown that cavernous malformations may be localized in almost every region of the brain as well as in the spinal cord. Spinal cord cavernous malformations (SCCM) have been diagnosed more frequently since magnetic resonance imaging (MRI) has become mmore widely available, Most are asymptomatic but may present as a diagnostic challenge with diffuse symptoms ranging from mere sensory deficits to paraparesis possibly affecting both upper and lower motor neuron. A 29-year-old Arabian man was admitted to the hospital with a progressive sensory loss to light touch, pink prick and vibration of the right and in a lesser extent of the left leg without any association to a particular dermatome. He additionally presented with progressing paresthesias in both legs, unsteady gait and incipient bladder- and bowl incontinence starting approximately 1 week prior to admission. Spinal MRI Showed a central, slightly lateralized intramedullary lesion 1 cm in diameter located within the conus medullaris that was suspicious for an intramedullary cavernous malformation. The lesion was accompanied by a perifocal edema and showed an inhomogenous hypointense core on T2W1 consistent with an acute cavernous hemorrhage. Treatment of symptomatic intramedullary cavernous angiomas should, if possible, consist of total surgical excision. It is essential to achieve complete removal during the first operation to avoid any residues that may lead to further bleeding. [ABSTRACT FROM AUTHOR]
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- 2006
171. Involvement of reactive oxygen species in the preservation injury to cultured liver endothelial cells
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Rauen, U., Elling, B., Gizewski, E. R., Korth, H.-G., Sustmann, R., and Groot, H. De
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- 1997
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172. Indication, Technique and Benefit of Intraoperative Spinal Digital Subtraction Angiography with a new Setting in a Patient with Spinal Arteriovenous Malformation
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Grams, A. E., Gizewski, E. R., Sandalcioglu, I. E., Forsting, M., and Sure, U.
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- 2011
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173. Brain response to visual sexual stimuli in homosexual pedophiles
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Boris Schiffer, Krueger, T., Paul, T., Greiff, A., Forsting, M., Leygraf, N., Schedlowski, M., and Gizewski, E.
174. Dopaminergic treatment modulates functional brain connectivity in restless legs syndrome
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Tuovinen, N., Stefani, A., Mitterling, T., Anna Heidbreder, Frauscher, B., Gizewski, E., Poewe, W., Hoegl, B., and Scherfler, C.
175. FUNCTIONAL BRAIN CONNECTIVITY ALTERATIONS IN RESTLESS LEGS SYNDROME ARE MODULATED BY DOPAMINERGIC MEDICATION
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Noora Tuovinen, Stefani, A., Mitterling, T., Heidbreder, A., Frauscher, B., Gizewski, E. R., Poewe, W., Hoegl, B., and Scherfler, C.
176. Complete Endovascular Occlusion of a Cranial Dural Fistula using a Venous “To the Point” Approach
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Gizewski, E. R., Göricke, S. L., Özkan, N., Grams, A. E., Ladd, M. E., Sure, U., and Forsting, M.
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- 2011
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177. Feed-forward neural networks using cerebral MR spectroscopy and DTI might predict neurodevelopmental outcome in preterm neonates.
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Janjic, T., Pereverzyev, S., Hammerl, M., Neubauer, V., Lerchner, H., Wallner, V., Steiger, R., Kiechl-Kohlendorfer, U., Zimmermann, M., Buchheim, A., Grams, A. E., and Gizewski, E. R.
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DIFFUSION tensor imaging , *PROTON magnetic resonance spectroscopy , *PREMATURE infants , *NEWBORN infants , *SPECTRUM analysis - Abstract
Objectives: We aimed to evaluate the ability of feed-forward neural networks (fNNs) to predict the neurodevelopmental outcome (NDO) of very preterm neonates (VPIs) at 12 months corrected age by using biomarkers of cerebral MR proton spectroscopy (1H-MRS) and diffusion tensor imaging (DTI) at term-equivalent age (TEA). Methods: In this prospective study, 300 VPIs born before 32 gestational weeks received an MRI scan at TEA between September 2013 and December 2017. Due to missing or poor-quality spectroscopy data and missing neurodevelopmental tests, 173 VPIs were excluded. Data sets consisting of 103 and 115 VPIs were considered for prediction of motor and cognitive developmental delay, respectively. Five metabolite ratios and two DTI characteristics in six different areas of the brain were evaluated. A feature selection algorithm was developed for receiving a subset of characteristics prevalent for the VPIs with a developmental delay. Finally, the predictors were constructed employing multiple fNNs and fourfold cross-validation. Results: By employing the constructed fNN predictors, we were able to predict cognitive delays of VPIs with 85.7% sensitivity, 100% specificity, 100% positive predictive value (PPV) and 99.1% negative predictive value (NPV). For the prediction of motor delay, we achieved a sensitivity of 76.9%, a specificity of 98.9%, a PPV of 90.9% and an NPV of 96.7%. Conclusion: FNNs might be able to predict motor and cognitive development of VPIs at 12 months corrected age when employing biomarkers of cerebral 1H-MRS and DTI quantified at TEA. Key Points: • A feed-forward neuronal network is a promising tool for outcome prediction in premature infants. • Cerebral proton magnetic resonance spectroscopy and diffusion tensor imaging can be used for the construction of early prognostic biomarkers. • Premature infants that would most benefit from early intervention services can be spotted at the time of optimal neuroplasticity. [ABSTRACT FROM AUTHOR]
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- 2020
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178. Development and Validation of Automated <scp>Magnetic Resonance</scp> Parkinsonism Index 2.0 to Distinguish <scp>Progressive Supranuclear Palsy‐Parkinsonism</scp> From <scp>Parkinson's Disease</scp>
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Andrea Quattrone, Maria G. Bianco, Angelo Antonini, David E. Vaillancourt, Klaus Seppi, Roberto Ceravolo, Antonio P. Strafella, Gioacchino Tedeschi, Alessandro Tessitore, Roberto Cilia, Maurizio Morelli, Salvatore Nigro, Basilio Vescio, Pier Paolo Arcuri, Rosa De Micco, Mario Cirillo, Luca Weis, Eleonora Fiorenzato, Roberta Biundo, Roxana G. Burciu, Florian Krismer, Nikolaus R. McFarland, Christoph Mueller, Elke R. Gizewski, Mirco Cosottini, Eleonora Del Prete, Sonia Mazzucchi, Aldo Quattrone, Quattrone, A., Bianco, M. G., Antonini, A., Vaillancourt, D. E., Seppi, K., Ceravolo, R., Strafella, A. P., Tedeschi, G., Tessitore, A., Cilia, R., Morelli, M., Nigro, S., Vescio, B., Arcuri, P. P., De Micco, R., Cirillo, M., Weis, L., Fiorenzato, E., Biundo, R., Burciu, R. G., Krismer, F., Mcfarland, N. R., Mueller, C., Gizewski, E. R., Cosottini, M., Del Prete, E., and Mazzucchi, S.
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Magnetic Resonance Spectroscopy ,Parkinson's disease ,Magnetic Resonance Parkinsonism Index 2.0 ,Parkinson Disease ,automated MRI biomarker ,progressive supranuclear palsy-parkinsonism ,Magnetic Resonance Imaging ,eye diseases ,Diagnosis, Differential ,Parkinsonian Disorders ,Neurology ,Humans ,Paralysis ,Supranuclear Palsy, Progressive ,Neurology (clinical) - Abstract
Background: Differentiating progressive supranuclear palsy-parkinsonism (PSP-P) from Parkinson's disease (PD) is clinically challenging. Objective: This study aimed to develop an automated Magnetic Resonance Parkinsonism Index 2.0 (MRPI 2.0) algorithm to distinguish PSP-P from PD and to validate its diagnostic performance in two large independent cohorts. Methods: We enrolled 676 participants: a training cohort (n=346; 43 PSP-P, 194 PD, and 109 control subjects) from our center and an independent testing cohort (n=330; 62 PSP-P, 171 PD, and 97 control subjects) from an international research group. We developed a new in-house algorithm for MRPI 2.0 calculation and assessed its performance in distinguishing PSP-P from PD and control subjects in both cohorts using receiver operating characteristic curves. Results: The automated MRPI 2.0 showed excellent performance in differentiating patients with PSP-P from patients with PD and control subjects both in the training cohort (area under the receiver operating characteristic curve [AUC]=0.93 [95% confidence interval, 0.89–0.98] and AUC=0.97 [0.93–1.00], respectively) and in the international testing cohort (PSP-P versus PD, AUC=0.92 [0.87–0.97]; PSP-P versus controls, AUC=0.94 [0.90–0.98]), suggesting the generalizability of the results. The automated MRPI 2.0 also accurately distinguished between PSP-P and PD in the early stage of the diseases (AUC=0.91 [0.84–0.97]). A strong correlation (r=0.91, P < 0.001) was found between automated and manual MRPI 2.0 values. Conclusions: Our study provides an automated, validated, and generalizable magnetic resonance biomarker to distinguish PSP-P from PD. The use of the automated MRPI 2.0 algorithm rather than manual measurements could be important to standardize measures in patients with PSP-P across centers, with a positive impact on multicenter studies and clinical trials involving patients from different geographic regions. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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- 2022
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179. Carpal tunnel syndrome assessment with diffusion tensor imaging: Value of fractional anisotropy and apparent diffusion coefficient.
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Klauser, A. S., Abd Ellah, M., Kremser, C., Taljanovic, M., Schmidle, G., Gabl, M., Cartes-Zumelzu, F., Steiger, R., and Gizewski, E. R.
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CARPAL tunnel syndrome treatment , *CARPAL tunnel syndrome , *DIFFUSION tensor imaging , *ANISOTROPY , *NEURAL conduction , *PATIENTS - Abstract
Objectives: To quantitatively assess carpal tunnel syndrome (CTS) with DTI by evaluating two approaches to determine cut-off values.Methods: In forty patients with CTS diagnosis confirmed by nerve conduction studies (NCs) and 14 healthy subjects (mean age 58.54 and 57.8 years), cross-sectional area (CSA), apparent diffusion coefficient (ADC) and fractional anisotropy (FA) at single and multiple levels with intraobserver agreement were evaluated.Results: Maximum and mean CSA and FA showed significant differences between healthy subjects and patients (12.85 mm2 vs. 28.18 mm2, p < 0.001, and 0.613 vs. 0.524, p=0.007, respectively) (10.12 mm2 vs. 19.9 mm2, p<0.001 and 0.617 vs. 0.54, p=0.003, respectively), but not maximum and mean ADC (p > 0.05). For cut-off values, mean and maximum CSA showed the same sensitivity and specificity (93.3 %). However, mean FA showed better sensitivity than maximum FA (82.6 % vs. 73.9 %), but lower specificity (66.7 % vs. 80 %), and significant correlation for maximum CSA, 97 % (p < 0.01), with good correlation for maximum ADC and FA, 84.5 % (p < 0.01) and 62 % (p=0.056), respectively.Conclusions: CSA and FA showed significant differences between healthy subjects and patients. Single measurement at maximum CSA is suitable for FA determination. Key Points • DTI showed that FA is stronger than ADC for CTS diagnosis. • Single- and multiple-level approaches were compared to determine FA and ADC. • Single-level evaluation at the thickest MN cross-sectional area is sufficient. [ABSTRACT FROM AUTHOR]- Published
- 2018
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180. Association of superficial siderosis of the central nervous system and low pressure headache.
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Holle, D., Sandalcioglu, I. E., Gizewski, E. R., Asgari, S., Timmann, D., Diener, H. C., and Weimar, C.
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LETTERS to the editor , *CENTRAL nervous system injuries - Abstract
A letter to the editor is presented in response to an article about a 59 year-old male with superficial siderosis (SS) on his central nervous system and low pressure headache by D. Holle and colleagues in the 2007 issue.
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- 2008
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181. Endovascular stroke therapy in Austria: a nationwide 1-year experience.
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Serles, W., Gattringer, T., Mutzenbach, S., Seyfang, L., Trenkler, J., Killer ‐ Oberpfalzer, M., Deutschmann, H., Niederkorn, K., Wolf, F., Gruber, A., Hausegger, K., Weber, J., Thurnher, S., Gizewski, E., Willeit, J., Karaic, R., Fertl, E., Našel, C., Brainin, M., and Erian, J.
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PATIENT management , *STROKE treatment , *CEREBRAL infarction , *THROMBOLYTIC therapy , *DIAGNOSIS ,HEALTH management - Abstract
Background and purpose Based on a tight network of stroke units ( SUs) and interventional centres, endovascular treatment of acute major intracranial vessel occlusion has been widely implemented in Austria. Documentation of all patients in the nationwide SU registry has thereby become mandatory. Methods Demographic, clinical and interventional characteristics of patients who underwent endovascular treatment for acute ischaemic stroke in 11 Austrian interventional centres between 1 October 2013 and 30 September 2014 were analysed. Results In total, 301 patients (50.5% women; median age 70.5 years; median National Institutes of Health Stroke Scale score 17) were identified.193 patients (64.1%) additionally received intravenous thrombolysis. The most frequent vessel occlusion sites were the M1 segment of the middle cerebral artery ( n = 161, 53.5%), the intracranial internal carotid artery ( n = 60, 19.9%) and the basilar artery ( n = 40, 13.3%). Stent retrievers were used in 235 patients (78.1%) and adequate reperfusion (modified Thrombolysis in Cerebral Infarction scores 2b and 3, median onset to reperfusion time 254 min) was achieved in 242 patients (81.4%). Symptomatic intracranial haemorrhage occurred in 7%. 43.8% of patients ( n = 132) had good functional outcome (modified Rankin Scale score 0-2) and the mortality rate was 20.9% ( n = 63) after 3 months. Compared to the anterior circulation, vertebrobasilar stroke patients had higher mortality. Patients with secondary hospital transportation had better outcomes after 3 months than in-house treated patients. Conclusion Our results document nationwide favourable outcome and safety rates of endovascular stroke treatment comparable to recent randomized trials. The ability to provide such data and the need to further optimize such an approach also underscore the contribution of respective registries. [ABSTRACT FROM AUTHOR]
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- 2016
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182. Second asymptomatic carotid surgery trial (ACST-2): a randomised comparison of carotid artery stenting versus carotid endarterectomy
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Alison Halliday, Richard Bulbulia, Leo H Bonati, Johanna Chester, Andrea Cradduck-Bamford, Richard Peto, Hongchao Pan, John Potter, Hans Henning Eckstein, Barbara Farrell, Marcus Flather, Averil Mansfield, Boby Mihaylova, Kazim Rahimi, David Simpson, Dafydd Thomas, Peter Sandercock, Richard Gray, Andrew Molyneux, Cliff P Shearman, Peter Rothwell, Anna Belli, Will Herrington, Parminder Judge, Peter Leopold, Marion Mafham, Michael Gough, Piergiorgio Cao, Sumaira MacDonald, Vasha Bari, Clive Berry, S Bradshaw, Wojciech Brudlo, Alison Clarke, Robin Cox, Susan Fathers, Kamran Gaba, Mo Gray, Elizabeth Hayter, Constance Holliday, Rijo Kurien, Michael Lay, Steffi le Conte, Jessica McManus, Zahra Madgwick, Dylan Morris, Andrew Munday, Sandra Pickworth, Wiktor Ostasz, Michiel Poorthuis, Sue Richards, Louisa Teixeira, Sergey Tochlin, Lynda Tully, Carol Wallis, Monique Willet, Alan Young, Renato Casana, Chiara Malloggi, Andrea Odero Jr, Vincenzo Silani, Gianfranco Parati, Giuseppe Malchiodi, Giovanni Malferrari, Francesco Strozzi, Nicola Tusini, Enrico Vecchiati, Gioacchino Coppi, Antonio Lauricella, Roberto Moratto, Roberto Silingardi, Jessica Veronesi, Andrea Zini, Emanuele Ferrero, Michelangelo Ferri, Andrea Gaggiano, Carmelo Labate, Franco Nessi, Daniele Psacharopulo, Andrea Viazzo, Giovanni Malacrida, Daniela Mazzaccaro, Giovanni Meola, Alfredo Modafferi, Giovanni Nano, Maria Teresa Occhiuto, Paolo Righini, Silvia Stegher, Stefano Chiarandini, Filippo Griselli, Sandro Lepidi, Fabio Pozzi Mucelli, Marcello Naccarato, Mario D'Oria, Barbara Ziani, Andrea Stella, Mortalla Dieng, Gianluca Faggioli, Mauro Gargiulo, Sergio Palermo, Rodolfo Pini, Giovanni Maria Puddu, Andrea Vacirca, Domenico Angiletta, Claudio Desantis, Davide Marinazzo, Giovanni Mastrangelo, Guido Regina, Raffaele Pulli, Paolo Bianchi, Lea Cireni, Elisabetta Coppi, Rocco Pizzirusso, Filippo Scalise, Giovanni Sorropago, Valerio Tolva, Valeria Caso, Enrico Cieri, Paola DeRango, Luca Farchioni, Giacomo Isernia, Massimo Lenti, Gian Battista Parlani, Guglielmo Pupo, Grazia Pula, Gioele Simonte, Fabio Verzini, Federico Carimati, Maria Luisa Delodovici, Federico Fontana, Gabriele Piffaretti, Matteo Tozzi, Efrem Civilini, Giorgio Poletto, Bernhard Reimers, Barbara Praquin, Sonia Ronchey, Laura Capoccia, Wassim Mansour, Enrico Sbarigia, Francesco Speziale, Pasqualino Sirignano, Danilo Toni, Roberto Galeotti, Vincenzo Gasbarro, Francesco Mascoli, Tiberio Rocca, Elpiniki Tsolaki, Giulia Bernardini, Ester DeMarco, Alessia Giaquinta, Francesco Patti, Massimiliano Veroux, Pierfrancesco Veroux, Carla Virgilio, Nicola Mangialardi, Matteo Orrico, Vincenzo Di Lazzaro, Nunzio Montelione, Francesco Spinelli, Francesco Stilo, Carlo Cernetti, Sandro Irsara, Giuseppe Maccarrone, Diego Tonello, Adriana Visonà, Beniamino Zalunardo, Emiliano Chisci, Stefano Michelagnoli, Nicola Troisi, Maela Masato, Massimo Dei Negri, Andrea Pacchioni, Salvatore Saccà, Giovanni Amatucci, Alfredo Cannizzaro, Federico Accrocca, Cesare Ambrogi, Renzo Barbazza, Giustino Marcucci, Andrea Siani, Guido Bajardi, Giovanni Savettieri, Angelo Argentieri, Riccardo Corbetta, Attilio Odero, Pietro Quaretti, Federico Z Thyrion, Alessandro Cappelli, Domenico Benevento, Gianmarco De Donato, Maria Agnese Mele, Giancarlo Palasciano, Daniela Pieragalli, Alessandro Rossi, Carlo Setacci, Francesco Setacci, Domenico Palombo, Maria Cecilia Perfumo, Edoardo Martelli, Aldo Paolucci, Santi Trimarchi, Viviana Grassi, Luigi Grimaldi, Giuliana La Rosa, Domenico Mirabella, Matteo Scialabba, Leonildo Sichel, Costantino L D'Angelo, Gian Franco Fadda, Holta Kasemi, Mario Marino, Francesco Burzotta, Francesco Alberto Codispoti, Angela Ferrante, Giovanni Tinelli, Yamume Tshomba, Claudio Vincenzoni, Deborah Amis, Dawn Anderson, Martin Catterson, Mike Clarke, Michelle Davis, Anand Dixit, Alexander Dyker, Gary Ford, Ralph Jackson, Sreevalsan Kappadath, David Lambert, Tim Lees, Stephen Louw, James McCaslin, Noala Parr, Rebecca Robson, Gerard Stansby, Lucy Wales, Vera Wealleans, Lesley Wilson, Michael Wyatt, Hardeep Baht, Ibrahim Balogun, Ilse Burger, Tracy Cosier, Linda Cowie, Gunaratnam Gunathilagan, David Hargroves, Robert Insall, Sally Jones, Hannah Rudenko, Natasha Schumacher, Jawaharlal Senaratne, George Thomas, Audrey Thomson, Tom Webb, Ellen Brown, Bernard Esisi, Ali Mehrzad, Shane MacSweeney, Norman McConachie, Alison Southam, Wayne Sunman, Ahmed Abdul-Hamiq, Jenny Bryce, Ian Chetter, Duncan Ettles, Raghuram Lakshminarayan, Kim Mitchelson, Christopher Rhymes, Graham Robinson, Paul Scott, Alison Vickers, Ray Ashleigh, Stephen Butterfield, Ed Gamble, Jonathan Ghosh, Charles N McCollum, Mark Welch, Sarah Welsh, Leszek Wolowczyk, Mary Donnelly, Stephen D'Souza, Anselm A Egun, Bindu Gregary, Thomas Joseph, Christine Kelly, Shuja Punekar, M Asad Rahi, Sonia Raj, Dare Seriki, George Thomson, James Brown, Ragunath Durairajan, Iris Grunwald, Paul Guyler, Paula Harman, Matthew Jakeways, Christopher Khuoge, Ashish Kundu, Thayalini Loganathan, Nisha Menon, Raji O Prabakaran, Devesh Sinha, Vicky Thompson, Sharon Tysoe, Dennis Briley, Chris Darby, Linda Hands, Dominic Howard, Wilhelm Kuker, Ursula Schulz, Rachel Teal, David Barer, Andrew Brown, Susan Crawford, Paul Dunlop, Ramesh Krishnamurthy, Nikhil Majmudar, Duncan Mitchell, Min P Myint, Richard O'Brien, Janice O'Connell, Naweed Sattar, Shanmugam Vetrivel, Jonathan Beard, Trevor Cleveland, Peter Gaines, John Humphreys, Alison Jenkins, Craig King, Daniel Kusuma, Ralph Lindert, Robbie Lonsdale, Raj Nair, Shah Nawaz, Faith Okhuoya, Douglas Turner, Graham Venables, Paul Dorman, Andrea Hughes, Deborah Jones, David Mendelow, Helen Rodgers, Aidas Raudoniitis, Peter Enevoldson, Hans Nahser, Imelda O'Brien, Francesco Torella, Dave Watling, Richard White, Pauline Brown, Dipankar Dutta, Lorraine Emerson, Paula Hilltout, Sachin Kulkarni, Jackie Morrison, Keith Poskitt, Fiona Slim, Sarah Smith, Amanda Tyler, Joanne Waldron, Mark Whyman, Milda Bajoriene, Lucy 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Golovkova M.S., Komakha B.B., Zherdev N.N., Belyasnik A., Chechulov P., Kandyba D., Stepanishchev I., Csobay-Novak C., Dosa E., Entz L., Nemes B., Szeberin Z., Barzo P., Bodosi M., Fako E., Fulop B., Nemeth T., Pazdernyik S., Skoba K., Voros E., Chatzinikou E., Giannoukas A., Karathanos C., Koutsias S., Kouvelos G., Matsagkas M., Ralli S., Rountas C., Rousas N., Spanos K., Brountzos E., Kakisis J.D., Lazaris A., Moulakakis K.G., Stefanis L., Tsivgoulis G., Vasdekis S., Antonopoulos C.N., Bellenis I., Maras D., Polydorou A., Polydorou V., Tavernarakis A., Ioannou N., Terzoudi M., Lazarides M., Mantatzis M., Vadikolias K., Dzieciuchowicz L., Gabriel M., Krasinski Z., Oszkinis G., Pukacki F., Slowinski M., Stanisic M.-G., Staniszewski R., Tomczak J., Zielinski M., Myrcha P., Rozanski D., Drelichowski S., Iwanowski W., Koncewicz K., Bialek P., Biejat Z., Czepel W., Czlonkowska A., Dowzenko A., Jedrzejewska J., Kobayashi A., Leszczynski J., Malek A., Polanski J., Proczka R., Skorski M., Szostek M., Andziak P., Dratwicki M., Gil R., Nowicki M., Pniewski J., Rzezak J., Seweryniak P., Dabek P., Juszynski M., Madycki G., Pacewski B., Raciborski W., Slowinski P., Staszkiewicz W., Bombic M., Chlouba V., Fiedler J., Hes K., Kostal P., Sova J., Kriz Z., Privara M., Reif M., Staffa R., Vlachovsky R., Vojtisek B., Hrbac T., Kuliha M., Prochazka V., Roubec M., Skoloudik D., Netuka D., Steklacova A., Benes III V., Buchvald P., Endrych L., Sercl M., Campos W., Casella I.B., de Luccia N., Estenssoro A.E.V., Presti C., Puech-Leao P., Neves C.R.B., da Silva E.S., Sitrangulo C.J., Monteiro J.A.T., Tinone G., Bellini Dalio M., Joviliano E.E., Pontes Neto O.M., Serra Ribeiro M., Cras P., Hendriks J.M.H., Hoppenbrouwers M., Lauwers P., Loos C., Yperzeele L., Geenens M., Hemelsoet D., van Herzeele I., Vermassen F., Astarci P., Hammer F., Lacroix V., Peeters A., Verhelst R., Cirelli S., Dormal P., Grimonprez A., Lambrecht B., Lerut P., Thues E., De Koster G., Desiron Q., Maertens de Noordhout A., Malmendier D., Massoz M., Saad G., Bosiers M., Callaert J., Deloose K., Blanco Canibano E., Garcia Fresnillo B., Guerra Requena M., Morata Barrado P.C., Muela Mendez M., Yusta Izquierdo A., Aparici Robles F., Blanes Orti P., Garcia Dominguez L., Martinez Lopez R., Miralles Hernandez M., Tembl Ferrairo J.I., Chamorro A., Macho J., Obach V., Riambau V., San Roman L., Ahlhelm F.J., Blackham K., Engelter S., Eugster T., Gensicke H., Gurke L., Lyrer P., Mariani L., Maurer M., Mujagic E., Muller M., Psychogios M., Stierli P., Stippich C., Traenka C., Wolff T., Wagner B., Wiegert M.M., Clarke S., Diepers M., Grochenig E., Gruber P., Isaak A., Kahles T., Marti R., Nedeltchev K., Remonda L., Tissira N., Valenca Falcao M., de Borst G.J., Lo R.H., Moll F.L., Toorop R., van der Worp B.H., Vonken E.J., Kappelle J.L., Jahrome O., Vos F., Schuiling W., van Overhagen H., Keunen R.W.M., Knippenberg B., Wever J.J., Lardenoije J.W., Reijnen M., Smeets L., van Sterkenburg S., Fraedrich G., Gizewski E., Gruber I., Knoflach M., Kiechl S., Rantner B., Abdulamit T., Bergeron P., Padovani R., Trastour J.-C., Cardon J.-M., Le Gallou-Wittenberg A., Allaire E., Becquemin J.-P., Cochennec-Paliwoda F., Desgranges P., Hosseini H., Kobeiter H., Marzelle J., Almekhlafi M.A., Bal S., Barber P.A., Coutts S.B., Demchuk A.M., Eesa M., Gillies M., Goyal M., Hill M.D., Hudon M.E., Jambula A., Kenney C., Klein G., McClelland M., Mitha A., Menon B.K., Morrish W.F., Peters S., Ryckborst K.J., Samis G., Save S., Smith E.E., Stys P., Subramaniam S., Sutherland G.R., Watson T., Wong J.H., Zimmel L., Flis V., Matela J., Miksic K., Milotic F., Mrdja B., Stirn B., Tetickovic E., Gasparini M., Grad A., Kompara I., Milosevic Z., Palmiste V., Toomsoo T., Aidashova B., Kospanov N., Lyssenko R., Mussagaliev D., Beyar R., Hoffman A., Karram T., Kerner A., Nikolsky E., Nitecki S., Andonova S., Bachvarov C., Petrov V., Cvjetko I., Vidjak V., Haluzan D., Petrunic M., Liu B., Liu C.-W., Bartko D., Beno P., Rusnak F., Zelenak K., Ezura M., Inoue T., Kimura N., Kondo R., Matsumoto Y., Shimizu H., Endo H., Furui E., Bakke S., Krohg-Sorensen K., Nome T., Skjelland M., Tennoe B., Albuquerque e Castro J., Alves G., Bastos Goncalves F., de Aragao Morais J., Garcia A.C., Valentim H., Vasconcelos L., Belcastro F., Cura F., Zaefferer P., Abd-Allah F., Eldessoki M.H., Heshmat Kassem H., Soliman Gharieb H., Colgan M.P., Haider S.N., Harbison J., Madhavan P., Moore D., Shanik G., Kazan V., Nazzal M., Ramsey-Williams V., and Gargiulo M
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Male ,medicine.medical_specialty ,Time Factors ,Time Factor ,medicine.medical_treatment ,Carotid Stenosi ,MEDLINE ,Carotid endarterectomy ,Rate ratio ,Risk Assessment ,Asymptomatic ,law.invention ,Randomized controlled trial ,law ,Risk Factors ,carotid artery stenting (CAS) ,carotid endarterectomy (CEA) ,Stent ,medicine ,Humans ,Carotid Stenosis ,Stroke ,Endarterectomy ,Aged ,Endarterectomy, Carotid ,business.industry ,carotid artery ,Risk Factor ,Articles ,General Medicine ,trial ,medicine.disease ,Settore MED/22 - CHIRURGIA VASCOLARE ,Surgery ,Stenosis ,Treatment Outcome ,Settore MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE ,Female ,Stents ,Human medicine ,medicine.symptom ,business ,Human - Abstract
Summary Background Among asymptomatic patients with severe carotid artery stenosis but no recent stroke or transient cerebral ischaemia, either carotid artery stenting (CAS) or carotid endarterectomy (CEA) can restore patency and reduce long-term stroke risks. However, from recent national registry data, each option causes about 1% procedural risk of disabling stroke or death. Comparison of their long-term protective effects requires large-scale randomised evidence. Methods ACST-2 is an international multicentre randomised trial of CAS versus CEA among asymptomatic patients with severe stenosis thought to require intervention, interpreted with all other relevant trials. Patients were eligible if they had severe unilateral or bilateral carotid artery stenosis and both doctor and patient agreed that a carotid procedure should be undertaken, but they were substantially uncertain which one to choose. Patients were randomly allocated to CAS or CEA and followed up at 1 month and then annually, for a mean 5 years. Procedural events were those within 30 days of the intervention. Intention-to-treat analyses are provided. Analyses including procedural hazards use tabular methods. Analyses and meta-analyses of non-procedural strokes use Kaplan-Meier and log-rank methods. The trial is registered with the ISRCTN registry, ISRCTN21144362. Findings Between Jan 15, 2008, and Dec 31, 2020, 3625 patients in 130 centres were randomly allocated, 1811 to CAS and 1814 to CEA, with good compliance, good medical therapy and a mean 5 years of follow-up. Overall, 1% had disabling stroke or death procedurally (15 allocated to CAS and 18 to CEA) and 2% had non-disabling procedural stroke (48 allocated to CAS and 29 to CEA). Kaplan-Meier estimates of 5-year non-procedural stroke were 2·5% in each group for fatal or disabling stroke, and 5·3% with CAS versus 4·5% with CEA for any stroke (rate ratio [RR] 1·16, 95% CI 0·86–1·57; p=0·33). Combining RRs for any non-procedural stroke in all CAS versus CEA trials, the RR was similar in symptomatic and asymptomatic patients (overall RR 1·11, 95% CI 0·91–1·32; p=0·21). Interpretation Serious complications are similarly uncommon after competent CAS and CEA, and the long-term effects of these two carotid artery procedures on fatal or disabling stroke are comparable. Funding UK Medical Research Council and Health Technology Assessment Programme.
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- 2021
183. Are there sex differences in placebo analgesia during visceral pain processing? A fMRI study in healthy subjects.
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Theysohn, N., Schmid, J., Icenhour, A., Mewes, C., Forsting, M., Gizewski, E. R., Schedlowski, M., Elsenbruch, S., and Benson, S.
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VISCERAL pain , *ANALGESIA , *FUNCTIONAL magnetic resonance imaging , *GENDER specific care , *PLACEBOS , *THERAPEUTICS - Abstract
Background We explored sex differences in the neural mechanisms mediating placebo analgesia in an established visceral pain model involving painful rectal distensions in healthy volunteers. Methods N = 15 men and N = 15 women underwent three consecutive functional magnetic resonance imaging sessions during which cued painful rectal distensions were delivered. After an adaptation session, positive expectations were induced with deceptive instructions regarding administration of an analgesic drug (placebo session). In the other session (control), truthful information about an inert substance was given. Sex differences in placebo-induced modulation of neural activation during anticipation and pain were analyzed along with ratings of expected and perceived pain intensity. Key Results Placebo-induced reductions in pain ratings were comparable between men and women. At the level of the brain, group comparisons with respect to differences between the placebo and control conditions revealed greater modulation of the posterior insula (regions-of-interest analysis: pFWE < 0.05) and dorsolateral prefrontal cortex (whole-brain analysis: p < 0.001, uncorrected) during pain anticipation in women. During pain, placebo-induced down-regulation of the insula was altered in women compared to men ( ROI analysis: pFWE < 0.05). Conclusions & Inferences Our data provide first evidence supporting sex differences in pain-induced neural modulation during visceral placebo analgesia despite similar placebo-induced reductions in perceived pain intensity. These preliminary findings might contribute to elucidating mechanisms mediating placebo effects in clinical conditions associated with chronic abdominal pain such as in irritable bowel syndrome. [ABSTRACT FROM AUTHOR]
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- 2014
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184. Location and Restoration of Function after Cerebellar Tumor Removal-A Longitudinal Study of Children and Adolescents.
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Küper, M., Döring, K., Spangenberg, C., Konczak, J., Gizewski, E., Schoch, B., and Timmann, D.
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LONGITUDINAL method , *CEREBELLAR nuclei , *MOTOR neurons , *MAGNETIC resonance imaging of the brain , *AGE groups , *CEREBELLAR ataxia - Abstract
Sequelae in children following cerebellar tumor removal surgery are well defined, and predictors for poor recovery include lesions of the cerebellar nuclei and the inferior vermis. Dynamic reorganization is thought to promote functional recovery in particular within the first year after surgery. Yet, the time course and mechanisms of recovery within this critical time frame are elusive and longitudinal studies are missing. Thus, a group of children and adolescents ( n = 12, range 6-17 years) were followed longitudinally after cerebellar surgery and compared to age- and gender-matched controls ( n = 11). Patients were examined (1) within the first days, (2) 3 months, and (3) 1 year after surgery. Each time behavioral tests of balance and upper limb motor function, ataxia rating, and a MRI scan were performed. Data were used for subsequent lesion-symptom mapping of cerebellar function. Behavioral improvements continued beyond 3 months, but were not complete in all patients after 1 year. At that time, remaining deficits were mild. Within the first 3 months, cerebellar lesion volumes were notably reduced by vanishing edema. Reduction in edema affecting the deep cerebellar nuclei but not reduction of total cerebellar lesion volume was a major predictor of early functional recovery. Persistent impairment in balance and upper limb function was linked to permanent lesions of the inferior vermis and the deep cerebellar nuclei. [ABSTRACT FROM AUTHOR]
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- 2013
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185. Perceived treatment group affects behavioral and neural responses to visceral pain in a deceptive placebo study.
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Kotsis, V., Benson, S., Bingel, U., Forsting, M., Schedlowski, M., Gizewski, E. R., and Elsenbruch, S.
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RECTAL diseases , *PLACEBOS , *ANALGESIA , *PAIN , *ANALGESICS - Abstract
Background To assess effects of perceived treatment (i.e. drug vs placebo) on behavioral and neural responses to rectal pain stimuli delivered in a deceptive placebo condition. Methods This fMRI study analyzed the behavioral and neural responses during expectation-mediated placebo analgesia in a rectal pain model. In N = 36 healthy subjects, the blood oxygen level-dependent (BOLD) response during cued anticipation and painful stimulation was measured after participants were informed that they had a 50% chance of receiving either a potent analgesic drug or an inert substance (i.e., double-blind administration). In reality, all received placebo. We compared responses in subjects who retrospectively indicated that they received the drug and those who believed to have received placebo. Key Results 55.6% ( N = 20) of subjects believed that they had received a placebo, whereas 36.1% ( N = 13) believed that they had received a potent analgesic drug. Subjects who were uncertain (8.3%, N = 3) were excluded. Rectal pain-induced discomfort was significantly lower in the perceived drug treatment group ( P < 0.05), along with significantly reduced activation of the insular, the posterior and anterior cingulate cortices during pain anticipation, and of the anterior cingulate cortex during pain (all P < 0.05 in regions-of-interest analyses). Conclusions & Inferences Perceived treatment constitutes an important aspect in placebo analgesia. A more refined understanding of individual treatment expectations and perceived treatment allocation has multiple implications for the design and interpretation of clinical trials and experimental studies on placebo and nocebo effects. [ABSTRACT FROM AUTHOR]
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- 2012
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186. Structural gray and white matter changes in patients with HIV.
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Küper, Michael, Rabe, K., Esser, S., Gizewski, E. R., Husstedt, I. W., Maschke, M., and Obermann, M.
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HIV-positive persons , *PERIAQUEDUCTAL gray matter , *MORPHOMETRICS , *REGRESSION analysis , *ATROPHY , *MAGNETIC resonance imaging , *DEMENTIA - Abstract
In this cross-sectional study we used magnetic resonance imaging (MRI)-based voxel based morphometry (VBM) in a sample of HIV positive patients to detect structural gray and white matter changes. Forty-eight HIV positive subjects with ( n = 28) or without ( n = 20) cognitive deficits (mean age 48.5 ± 9.6 years) and 48 age- and sex-matched HIV negative controls underwent MRI for VBM analyses. Clinical testing in HIV patients included the HIV dementia scale (HDS), Unified Parkinson's Disease Rating Scale (UPDRS) and the grooved pegboard test. Comparing controls with HIV positive patients with cognitive dysfunction ( n = 28) VBM showed gray matter decrease in the anterior cingulate and temporal cortices along with white matter reduction in the midbrain region. These changes were more prominent with increasing cognitive decline, when assigning HIV patients to three cognitive groups (not impaired, mildly impaired, overtly impaired) based on performance in the HIV dementia scale. Regression analysis including all HIV positive patients with available data revealed that prefrontal gray matter atrophy in HIV was associated with longer disease duration ( n = 48), while motor dysfunction ( n = 48) was associated with basal ganglia gray matter atrophy. Lower CD4 cell count ( n = 47) correlated with decrease of occipital gray matter. Our results provide evidence for atrophy of nigro-striatal and fronto-striatal circuits in HIV. This pattern of atrophy is consistent with motor dysfunction and dysexecutive syndrome found in HIV patients with HIV-associated neurocognitive disorder. [ABSTRACT FROM AUTHOR]
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- 2011
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187. Lesion-Symptom Mapping of the Human Cerebellum.
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Timmann, D., Brandauer, B., Hermsdörfer, J., Ilg, W., Konczak, J., Gerwig, M., Gizewski, E., and Schoch, B.
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MAGNETIC resonance imaging , *CEREBELLAR nuclei , *CEREBELLUM , *BRAIN , *EFFERENT pathways - Abstract
High-resolution structural magnetic resonance imaging (MRI) has become a powerful tool in human cerebellar lesion studies. Structural MRI is helpful to analyse the localisation and extent of cerebellar lesions and to determine possible extracerebellar involvement. Functionally meaningful correlations between a cerebellar lesion site and behavioural data can be obtained both in subjects with degenerative as well as focal cerebellar disorders. In this review, examples are presented which demonstrate that MRI-based lesion-symptom mapping is helpful to study the function of cerebellar cortex and cerebellar nuclei. Behavioural measures were used which represent two main areas of cerebellar function, that is, motor coordination and motor learning. One example are correlations with clinical data which are in good accordance with the known functional compartmentalisation of the cerebellum in three sagittal zones: In patients with cerebellar cortical degeneration ataxia of stance and gait was correlated with atrophy of the medial (and intermediate) cerebellum, oculomotor disorders with the medial, dysarthria with the intermediate and limb ataxia with atrophy of the intermediate and lateral cerebellum. Similar findings were obtained in patients with focal lesions. In addition, in patients with acute focal lesions, a somatotopy in the superior cerebellar cortex was found which is in close relationship to animal data and functional MRI data in healthy control subjects. Finally, comparison of data in patients with acute and chronic focal lesions revealed that lesion site appears to be critical for motor recovery. Recovery after lesions to the nuclei of the cerebellum was less complete. Another example which extended knowledge about functional localisation within the cerebellum is classical conditioning of the eyeblink response, a simple form of motor learning. In healthy subjects, learning rate was related to the volume of the cortex of the posterior cerebellar lobe. In patients with focal cerebellar lesions, acquisition of eyeblink conditioning was significantly reduced in lesions including the cortex of the superior posterior lobe, but not the inferior posterior lobe. Disordered timing of conditioned eyeblink responses correlated with lesions of the anterior lobe. Findings are in good agreement with the animal literature. Different parts of the cerebellar cortex may be involved in acquisition and timing of conditioned eyeblink responses in humans. These examples demonstrate that MRI-based lesion-symptom mapping is helpful to study the contribution of functionally relevant cerebellar compartments in motor control and recovery in patients with cerebellar disease. In addition, information about the function of cerebellar cortex and nuclei can be gained. [ABSTRACT FROM AUTHOR]
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- 2008
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188. Increased basal-ganglia activation performing a non-dystonia-related task in focal dystonia.
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Obermann, M., Yaldizli, O., de Greiff, A., Konczak, J., Lachenmayer, M. L., Tumczak, F., Buhl, A. R., Putzki, N., Vollmer-Haase, J., Gizewski, E. R., Diener, H.-C., and Maschke, M.
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DYSTONIA , *BASAL ganglia , *SENSORIMOTOR cortex , *EYELID diseases , *CERVIX uteri diseases , *MAGNETIC resonance imaging - Abstract
Background and purpose: We tried to determine whether altered sensorimotor cortex and basal-ganglia activation in blepharospasm (BSP) and cervical dystonia (CD) are restricted to areas directly responsible for the innervation of dystonic muscles, or whether impairment in focal dystonia reaches beyond these direct associations supporting a more global disturbance of sensory and motor control in focal dystonia. Methods: Twenty patients with focal dystonia (11 BSP, 9 CD) and 14 healthy controls were investigated with functional magnetic resonance imaging (fMRI) performing a simple grip force forearm contraction task. Results: BSP and CD patients and healthy controls showed similar activation in the pre-motor, primary motor and primary sensory cortex, whilst basal-ganglia activation was increased in BSP and CD with related activation patterns compared with controls. BSP patients had increased activation in the thalamus, caudate nucleus, putamen and lateral globus pallidus, whilst CD patients showed increased activation in the caudate nucleus, putamen and thalamus. No differences in applied grip force were detected between groups. Conclusions: In both, BSP and CD, increased basal-ganglia activation could be demonstrated in a task not primarily involving the dystonic musculature affected by these disorders. Comparable activation changes may also indicate a common pathway in the pathophysiology in BSP and CD. [ABSTRACT FROM AUTHOR]
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- 2008
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189. Trace eyeblink conditioning in human subjects with cerebellar lesions.
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Gerwig, M., Haerter, K., Hajjar, K., Dimitrova, A., Maschke, M., Kolb, F., Thilmann, A., Gizewski, E., and Timmann, D.
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PRECANCEROUS conditions , *BRAIN diseases , *BLOOD vessels , *BRAIN stimulation , *STIMULUS compounding , *CONDITIONED response , *EYE - Abstract
Trace eyeblink conditioning was investigated in 31 patients with focal cerebellar lesions and 19 age-matched controls. Twelve patients presented with lesions including the territory of the superior cerebellar artery (SCA). In 19 patients lesions were restricted to the territory of the posterior inferior cerebellar artery (PICA). A 3D magnetic resonance imaging was used to determine the extent of the cortical lesion and possible involvement of cerebellar nuclei. Eyeblink conditioning was performed using a 40 ms tone as conditioned stimulus (CS) followed by a stimulus free trace-interval of 400 ms and a 100 ms air-puff as unconditioned stimulus (US). In SCA patients with lesions including parts of the cerebellar interposed nucleus trace eyeblink conditioning was significantly impaired. Pure cortical lesions of the superior cerebellum were not sufficient to reduce acquisition of trace conditioned eyeblink responses. PICA patients were not impaired in trace eyeblink conditioning. Consistent with animal studies the findings of the present human lesion study suggest that, in addition to forebrain areas, the interposed nucleus is of importance in trace eyeblink conditioning. Although cortical cerebellar areas appear less important in trace compared with delay eyeblink conditioning, the present data strengthen the view that cerebellar structures contribute to different forms of eyeblink conditioning paradigms. [ABSTRACT FROM AUTHOR]
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- 2006
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190. Incidence of dysarthria in children with cerebellar tumors: A prospective study.
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Richter, S., Schoch, B., Ozimek, A., Gorissen, B., Hein-Kropp, C., Kaiser, O., Hövel, M., Wieland, R., Gizewski, E., Ziegler, W., and Timmann, D.
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ARTICULATION disorders in children , *SPEECH disorders in children , *ARTICULATION disorders , *SPEECH disorders , *CHILDREN , *CEREBELLAR cortex , *TUMORS - Abstract
The present study investigated dysarthric symptoms in children with cerebellar tumors. Ten children with cerebellar tumors and 10 orthopedic control children were tested prior and one week after surgery. Clinical dysarthric symptoms were quantified in spontaneous speech. Syllable durations were analyzed in syllable repetition and sentence production tasks. Localization of the cerebellar lesions were defined after manual transfer from individual 2D-MR images onto 3D images of a spatially normalized healthy brain. Cerebellar children showed few and mild clinical signs of dysarthria. No difference was present in the sentence production task compared to controls. In five cerebellar children, syllables were prolonged in the syllable repetition task after surgery. Syllable duration normalized in an additional four-week session in all but one case. The MR-analysis showed that superior paravermal cerebellar areas likely involved in dysarthria in adults (paravermal lobules HVI, Crus I) were not significantly affected. In children, speech impairments appear to be rare after cerebellar surgery because tumors most commonly affect posterior-inferior and medial parts of the cerebellum while critical cerebellar regions are likely spared. The results suggest a similar localization of speech functions in the cerebellum in children and adults. [ABSTRACT FROM AUTHOR]
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- 2005
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191. Stimulus-response versus stimulus-stimulus-response learning in cerebellar patients.
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Richter, S., Matthies, K., Ohde, T., Dimitrova, A., Gizewski, E., Beck, A., Aurich, V., and Timmann, D.
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STIMULUS satiation , *MOTOR learning , *MAGNETIC resonance imaging , *PSYCHOLOGY of learning , *MEDICAL imaging systems , *MOVEMENT education - Abstract
Ample evidence exists that the cerebellum is involved in associative motor learning, particularly in eyeblink-conditioning. In visuomotor associative learning the role of the cerebellum is less clear. One open question is whether cerebellar patients’ deficits in visuomotor learning are present both in a stimulus-response and a stimulus-stimulus-response association task. Twelve patients with cerebellar degeneration and 12 healthy matched control subjects participated. A magnetic resonance imaging (MRI) volumetric analysis of the cerebellum was performed to assess the degree of cerebellar atrophy. In a blocked design, subjects had to learn the association between one color square or two color squares and a right or left key press. In the latter condition, the two colors were shown one after the other in the same sequence except for two blocks at the end of the experiment. Overall, cerebellar subjects reacted significantly slower than controls. In both groups, reaction time decreased over blocks, and the learning effect was more pronounced in the stimulus-response than in the stimulus-stimulus-response condition.Post hocanalyses revealed that learning differences between conditions were significant in cerebellar patients but not control subjects. Furthermore, only healthy subjects were irritated, i.e., they significantly increased reaction times in the blocks with reversed sequence in the stimulus-stimulus-response condition. Cerebellar subjects tended to name less correct stimulus-stimulus-response associations after the experiment. Finally, cerebellar volume correlated with parameters of motor performance, but not learning. In conclusion, cerebellar patients showed deficits in stimulus-stimulus-response, but not stimulus-response learning. Future experiments are needed to differentiate between possible deficits in learning the stimulus-stimulus association, use of sequence information, and/or impaired motor performance interfering with learning. [ABSTRACT FROM AUTHOR]
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- 2004
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192. Preserved verb generation in patients with cerebellar atrophy
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Richter, S., Kaiser, O., Hein-Kropp, C., Dimitrova, A., Gizewski, E., Beck, A., Aurich, V., Ziegler, W., and Timmann, D.
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CEREBELLUM diseases , *ARTICULATION disorders , *PATIENTS , *BRAIN - Abstract
A role of the right cerebellar hemisphere has been suggested in linguistic functions. Nevertheless, studies of verb generation in cerebellar patients provide inconsistent results. The aim of the present study was to examine verb generation in a larger group of cerebellar patients with well-defined lesions. Ten subjects with degenerative cerebellar disorders and ten healthy matched controls participated. Subjects had to generate verbs to the blocked presentation of photographs of objects (i.e. four blocks of sixteen objects). As control condition, the objects had to be named. Furthermore, dysarthria was quantified by means of a sentence production and syllable repetition task. Volumetric analysis of individual 3D-MR scans was performed to quantify cerebellar atrophy. Cerebellar patients were slower in the sentence production and syllable repetition tasks, and cerebellar volume was decreased compared to controls. Despite cerebellar atrophy and dysarthria, the answers produced did not differ between patients and controls. In addition, both groups revealed the same amount of decrease in verbal reaction time over blocks (i.e. learning). The results suggest that the role of the cerebellum in verb generation is less pronounced than previously suggested. [Copyright &y& Elsevier]
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- 2004
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193. Cerebellar mutism: Report of four cases.
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Ozimek, A., Richter, S., Hein-Kropp, C., Schoch, B., Goriβen, B., Kaiser, O., Gizewski, E., Ziegler, W., and Timmann, D.
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POSTERIOR fossa syndrome , *SPEECH disorders , *ARTICULATION disorders , *MOTOR ability , *CEREBELLAR tumors , *BRAIN tumors - Abstract
The aim of the present study was to investigate the manifestations of mutism after surgery in children with cerebellar tumors. Speech impairment following cerebellar mutism in children was investigated based on standardized acoustic speech parameters and perceptual criteria. Mutistic and non–mutistic children after cerebellar surgery as well as orthopedic controls were tested pre–and postoperatively. Speech impairment was compared with the localization of cerebellar lesions (i. e. affected lobules and nuclei). Whereas both control groups showed no abnormalities in speech and behavior, the mutistic group could be divided into children with dysarthria in post mutistic phase and children with mainly behavioral disturbances. In the mutistic children involvement of dentate and fastigial nuclei tended to be more frequent and extended than in the nonmutistic cerebellar children. Cerebellar mutism is a complex phenomenon of at least two types. Dysarthric symptoms during resolution of mutism support the anarthria hypothesis, while mainly behavioral changes suggest an explanation independent from speech motor control. [ABSTRACT FROM AUTHOR]
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- 2004
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194. Multimodal MRI reveals alterations of sensorimotor circuits in restless legs syndrome.
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Stefani, A., Mitterling, T., Heidbreder, A., Steiger, R., Kremser, C., Frauscher, B., Gizewski, E., Poewe, W., Högl, B., and Scherfler, C.
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RESTLESS legs syndrome , *DIFFUSION tensor imaging , *WHITE matter (Nerve tissue) , *SENSORIMOTOR cortex , *PREMOTOR cortex - Published
- 2019
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195. SP 10. Innsbruck experience in neuropathic pain syndromes: Re-think and re-construct old methods for better results.
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Eisner, W., Sohm, F., Rehwald, R., Scharnboeck, L., Siedentopf, C., Quirbach, S., Gizewski, E., and Kerschbaumer, J.
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NEUROPATHY , *PAIN management , *DEEP brain stimulation , *MOVEMENT disorders , *PARKINSON'S disease , *ESSENTIAL tremor - Abstract
Introduction In the last 25 years neuromodulation by deep brain stimulation gained widely acceptance starting in the field of movement disorders and getting further indications in pain syndroms and mood disorders. Surgical interventions should only be considered being a treatment option after proving ineffectiveness of conservative therapy forms. The highly acclaimed success of deep brain stimulation in Parkinsons disease, essential tremor, dystonia, chorea huntington, tourette syndrome, cannot be translated 1:1 to neuropathic pain syndromes. The EFNS guidelines on neurostimulation therapy for neuropathic pain published in the European Journal of Neurology 2007; 14: 952–970 revealed DBS against pain to be less effective than in movement disorders. The publication identified several reviews and one meta-analysis, which conclude that DBS is more effective for nociceptive pain than for neuropathic pain (63% vs. 47% long-term success). In patients with neuropathic pain, moderately higher rates of success were seen in patients with peripheral lesions. Because neuropathic pain syndromes are a complex compilation of missing information in different pathways to and within the brain resulting in the different aspects of pain consisting of sensation, perception, mood, emotion and vegetative aspects. Material and methods We will demonstrate different neuropathic pain syndromes following neurosurgical stereotactic interventions for neuromodulation. We were able to enhance the reduced input to the consciousness of man and women by modulation of the two main input areas namely the sensory thalamus and the posterior limp of the internal capsule. We modified the implantation site in the internal capsule because of ineffectiveness of the historical target and an anatomical chaos in the literature on the anatomical construction of the posterior limp of the internal capsule. By doing so we are able to cover all essential afferent fibers to the sensori-motor and the parietal cortex. In comparison to all other methods or other implantation centers a minimum of 2 stimulation electrodes have to be implanted per cerebral hemisphere. 30 patients were treated by neuromodulation against neuropathic pain syndromes. Without motor cortex stimulation and deep brain stimulation against cluster headache we operated 18 patients against neuropathic pain syndromes with our two electrode method. 6 trigeminal neuropathia (5 analgesia dolorosa) patients, 4 peripheral nerve injury patients and 8 post stroke patients. Results All patients had at least 60% up to 100% pain reduction. Some patients developed a decrease of the stimulation effect by “overstimulation”. Intermittent stimulation and our method of intensity modulation is able to reduce habituation of stimulation effects. The anterior cingulate gyrus stimulation according to T. Aziz will complete the armentarium of deep brain stimulation against neuropathic pain syndromes. Prospective randomized double blind studies in neuromodulation against neuropathic pain are still missing and will be conducted in the near future. [ABSTRACT FROM AUTHOR]
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- 2016
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196. Affective disturbances modulate the neural processing of visceral pain stimuli in irritable bowel syndrome: an fMRI study.
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Elsenbruch, S., Rosenberger, C., Enck, P., Forsting, M., Schedlowski, M., and Gizewski, E. R.
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IRRITABLE colon , *ANXIETY , *PAIN , *MAGNETIC resonance imaging , *OXYGENATORS , *PREFRONTAL cortex - Abstract
Objective To address the role of anxiety and depression symptoms in altered pain processing in irritable bowel syndrome (IBS). Design In this functional magnetic resonance imaging study, the blood oxygen level-dependent (BOLD) response to rectal distensions delivered at previously determined individual discomfort thresholds was assessed. Patients 15 female patients with irritable bowel syndrome (IBS) and with normal rectal pain thresholds, and 12 healthy women. Measures The correlation of anxiety and depression symptoms, measured with the Hospital Anxiety and Depression Scale (HADS), with subjective pain ratings and the BOLD response during distension-induced brain activation were analysed within IBS. Group differences in pain-induced brain activation with and without controlling for HADS scores were evaluated. Results Patients with IBS experienced significantly more pain and discomfort upon rectal distensions in the scanner, despite unaltered rectal sensory thresholds. Anxiety and depression scores were associated with these subjective stimulus ratings, but not with rectal sensory thresholds. Anxiety symptoms in IBS were significantly associated with pain-induced activation of the anterior midcingulate cortex and pregenual anterior cingulate cortex. Depression scores correlated with activation of the prefrontal cortex (PFC) and cerebellar areas within IBS. Group comparisons with the two-sample t test revealed significant activation in the IBS versus controls contrast in the anterior insular cortex and PFC. Inclusion of anxiety and depression scores, respectively, as confounding variables led to a loss of significant group differences. Conclusions Altered central processing of visceral stimuli in IBS is at least in part mediated by symptoms of anxiety and depression, which may modulate the affective-motivational aspects of the pain response. [ABSTRACT FROM AUTHOR]
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- 2010
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197. Effects of psychological stress on the cerebral processing of visceral stimuli in healthy women.
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ROSENBERGER, C., ELSENBRUCH, S., SCHOLLE, A., DE GREIFF, A., SCHEDLOWSKI, M., FORSTING, M., and GIZEWSKI, E. R.
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PSYCHOLOGICAL stress , *WOMEN'S health , *MAGNETIC resonance imaging , *OXYGEN , *ANXIETY - Abstract
The aim of the study was to analyse effects of psychological stress on the neural processing of visceral stimuli in healthy women. The brain functional magnetic resonance imaging blood oxygen level-dependent response to non-painful and painful rectal distensions was recorded from 14 healthy women during acute psychological stress and a control condition. Acute stress was induced with a modified public speaking stress paradigm. State anxiety was assessed with the State-Trait-Anxiety Inventory; chronic stress was measured with the Perceived Stress Questionnaire. During non-painful distensions, activation was observed in the right posterior insular cortex (IC) and right S1. Painful stimuli revealed activation of the bilateral anterior IC, right S1, and right pregenual anterior cingulate cortex. Chronic stress score was correlated with activation of the bilateral amygdala, right posterior IC (post-IC), left periaqueductal grey (PAG), and right dorsal posterior cingulate gyrus (dPCC) during non-painful stimulation, and with activation of the right post-IC, right PAG, left thalamus (THA), and right dPCC during painful distensions. During acute stress, state anxiety was significantly higher and the acute stress – control contrast revealed activation of the right dPCC, left THA and right S1 during painful stimulation. This is the first study to demonstrate effects of acute stress on cerebral activation patterns during visceral pain in healthy women. Together with our finding that chronic stress was correlated wit the neural response to visceral stimuli, these results provide a framework for further studies addressing the role of chronic stress and emotional disturbances in the pathophysiology of visceral hyperalgesia. [ABSTRACT FROM AUTHOR]
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- 2009
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198. Sacral fracture associated with a Tarlov cyst causing an anterior sacral CSF fistula and intraventricular fat emboli - a case report and review of the literature.
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Kögl N, Thomé C, Gindlhuber K, Dazinger F, Gizewski E, Kiechl S, and Petr O
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- Female, Humans, Fistula etiology, Fistula surgery, Magnetic Resonance Imaging, Spinal Fractures complications, Spinal Fractures surgery, Spinal Fractures diagnostic imaging, Tomography, X-Ray Computed, Aged, Embolism, Fat etiology, Sacrum injuries, Tarlov Cysts complications
- Abstract
Background: Sacral fractures are rare and either associated with high-energy trauma or osteoporosis in most cases. A search of the current literature on sacral fractures and cerebrospinal fluid fistula identified only few cases. Pathological fractures are uncommon and exceedingly rare in case of Tarlov cysts. Sacral fractures can be missed in oligosymptomatic patients. However, severe complications may emerge as shown by this case report., Methods: We present the case of a pathological sacral fracture at the level S2/3 following a low-impact trauma, associated with a Tarlov cyst, which was complicated by an anterior CSF fistula and intraventricular fat emboli., Results: The patient was treated conservatively with strict bedrest and a CT-guided blood patch. Postponed mobilization was successful with decreasing orthostatic symptoms. Follow-up MRI and CT imaging showed a complete resolution of the ventral CSF fistula and ossification of the fracture. The intraventricular fat did not resolve, however, there was no radiological sign of hydrocephalus with excellent clinical outcome at 6-months follow-up., Conclusion: Although exceedingly rare, sacral Tarlov cysts may be associated with pathological fractures of the sacrum. Relevant complications can emerge and need to be properly addressed.
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- 2024
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199. Performance evaluation of machine-assisted interpretation of Gram stains from positive blood cultures.
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Walter C, Weissert C, Gizewski E, Burckhardt I, Mannsperger H, Hänselmann S, Busch W, Zimmermann S, and Nolte O
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- Humans, Blood Culture, Reproducibility of Results, Neural Networks, Computer, Yeasts, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization methods, Firmicutes, Sepsis diagnosis, Bacillus, Gentian Violet, Phenazines
- Abstract
Manual microscopy of Gram stains from positive blood cultures (PBCs) is crucial for diagnosing bloodstream infections but remains labor intensive, time consuming, and subjective. This study aimed to evaluate a scan and analysis system that combines fully automated digital microscopy with deep convolutional neural networks (CNNs) to assist the interpretation of Gram stains from PBCs for routine laboratory use. The CNN was trained to classify images of Gram stains based on staining and morphology into seven different classes: background/false-positive, Gram-positive cocci in clusters (GPCCL), Gram-positive cocci in pairs (GPCP), Gram-positive cocci in chains (GPCC), rod-shaped bacilli (RSB), yeasts, and polymicrobial specimens. A total of 1,555 Gram-stained slides of PBCs were scanned, pre-classified, and reviewed by medical professionals. The results of assisted Gram stain interpretation were compared to those of manual microscopy and cultural species identification by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). The comparison of assisted Gram stain interpretation and manual microscopy yielded positive/negative percent agreement values of 95.8%/98.0% (GPCCL), 87.6%/99.3% (GPCP/GPCC), 97.4%/97.8% (RSB), 83.3%/99.3% (yeasts), and 87.0%/98.5% (negative/false positive). The assisted Gram stain interpretation, when compared to MALDI-TOF MS species identification, also yielded similar results. During the analytical performance study, assisted interpretation showed excellent reproducibility and repeatability. Any microorganism in PBCs should be detectable at the determined limit of detection of 10
5 CFU/mL. Although the CNN-based interpretation of Gram stains from PBCs is not yet ready for clinical implementation, it has potential for future integration and advancement., Competing Interests: E.G., H.M., S.H., and W.B. are employees of MetaSystems Hard & Software GmbH. Metafer is provided to University Hospital Heidelberg and its employees, C. Walter, S.Z., and I.B., as part of a cooperation agreement free of charge.- Published
- 2024
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200. Noninvasive CSF shunt patency evaluation by superb microvascular imaging.
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Putzer D, Brawanski K, Verius M, Oberherber H, Thome C, Gizewski ER, and Gruber H
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- Humans, Angiography, Computer Simulation, Ventriculoperitoneal Shunt adverse effects, Hydrocephalus diagnostic imaging, Hydrocephalus surgery, Hydrocephalus etiology
- Abstract
Occlusion of a ventriculoperitoneal shunt system is a potentially life-threatening complication in patients suffering from hydrocephalus. However, there is no imaging established as standard approach in this acute setting. In the present study, we evaluate the use of superb microvascular imaging for investigation of the patency of ventriculoperitoneal shunt systems. Simulation of low flow rates of cerebrospinal fluid through a small diameter CSF shunt system was performed in a dedicated phantom in order to proof the principle of superb microvascular imaging (SMI) being feasible for the measurement of slow CSF flow through the dedicated CSF shunt system. SMI is able to detect low flow rates in CSF shunt systems effectively and fast. Visualization of a Duplex ultrasound flow and Doppler wave pattern in the VP shunt system after the reservoir has been pressed confirms patency. SMI is an effective method for evaluating CSF shunt patency and diagnosing shunt obstruction. This bears the potential to facilitate evaluation of clinically symptomatic VP shunt patients in an acute setting. Further evaluation of ultrasound flow patterns is granted., (© 2023. The Author(s).)
- Published
- 2023
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