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Journal articles on the topic 'Scan'

Author: Grafiati
Published: 4 June 2021
Last updated: 20 February 2023

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1

Dombrose, Fred, and S. Perkins. "Scan or Scam?" Science News 165, no. 25 (June 19, 2004): 399. http://dx.doi.org/10.2307/4015145.

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2

Sokolovsky, N., A. Cook, H. Hunt, P. Giunti, and L. Cipolotti. "A Preliminary Characterisation of Cognition and Social Cognition in Spinocerebellar Ataxia Types 2, 1, and 7." Behavioural Neurology 23, no. 1-2 (2010): 17–29. http://dx.doi.org/10.1155/2010/395045.

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Over the last decade, studies have implicated the cerebellum not only in motor functioning, but also in cognition and social cognition. Although some aspects of cognition have been explored in the five most common forms of Spinocerebellar Ataxia (SCA), social cognition in these patients has rarely been examined. The present study provides a preliminary characterisation of the severity of cognitive and social cognitive impairments in patients with SCA2, SCA1 and SCA7 using an identical battery to the one previously used in SCA3 and SCA6 patients for comparison. The cognitive profiles of SCA1 and SCA7 patients were comparable to that of SCA6 patients; SCA1 patients had relatively intact profiles, while SCA7 patients demonstrated only some selective deficits. In contrast, SCA2 patients showed the greatest impairments, similarly to SCA3 patients. On tests of social cognition, SCA2 and SCA7 patients were impaired on a task of emotion attribution, whereas one SCA1 patient had a Theory of Mind deficit, which has also been documented in SCA3 and SCA6. We provide preliminary evidence that the neuropsychological profiles of SCA patients correspond well with the severity of pathological and clinical features. Moreover, these patients may also have social cognition impairments. Overall, we suggest that there is a degree of heterogeneity in the types of cognitive and social cognitive impairments in SCA patients.
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3

Freund, Aline Andrade, Rosana Hermínia Scola, Hélio A. G. Teive, Raquel Cristina Arndt, Magda Clara Vieira da Costa-Ribeiro, Lupe Furtado Alle, and Lineu Cesar Werneck. "Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals." Arquivos de Neuro-Psiquiatria 67, no. 4 (December 2009): 1124–32. http://dx.doi.org/10.1590/s0004-282x2009000600034.

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The diagnosis and incidence of spinocerebelar ataxias (SCA) is sometimes difficult to analyze due the overlap of phenotypes subtypes and are disorders of mutations caused by CAG trinucleotide repeat expansion. To investigate the incidence of the SCA in Southern Brazil, we analyzed the trinucleotide repeats (CAG)n at the SCA1, SCA2, SCA3, SCA6 and SCA7 loci to identify allele size ranges and frequencies. We examined blood sample from 154 asymptomatic blood donors and 115 individuals with progressive ataxias. PCR products were submitted to capillary electrophoresis. In the blood donors, the ranges of the five loci were: SCA1, 19 to 36 (CAG)n; SCA2, 6 to 28 (CAG)n; SCA3, 12 to 34 (CAG)n; SCA6, 2 to 13 (CAG)n; and SCA7, 2 to 10 (CAG)n. No deviations from Hardy-Weinberg equilibrium were detected. In the ataxia group, we found (CAG)n above the range of the asymptomatic blood donors in SCA3 (21.74%) followed by SCA2 (5.22%), SCA7 (2.61%), SCA6 (0.87%), and no cases of SCA1. The remaining 80 cases (69.56%) have different diagnoses from the type here studied. These data defined the alleles and their frequencies, as well as demonstrated their stability in the population not affected. The molecular diagnosis test confirmed the clinical diagnosis in 28/45 cases and classified another 7/70 from the clinical unclassified ataxias group.
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4

Zinn, C. "Radiologists accused in "scan scam"." BMJ 319, no. 7218 (October 30, 1999): 1156. http://dx.doi.org/10.1136/bmj.319.7218.1156.

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5

Lopes-Cendes, Iscia, Carlos E. Steiner, Isabel Silveira, Walter Pinto-Junior, Jayme A. Maciel, and Guy A. Rouleau. "Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1." Arquivos de Neuro-Psiquiatria 54, no. 3 (September 1996): 412–18. http://dx.doi.org/10.1590/s0004-282x1996000300009.

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The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of late onset neurodegenerative disorders. To date, seven different genes causing autosomal dominant SCA have been mapped: SCA1, SCA2, Machado-Joseph disease (MJD)/SCA3, SCA4, SCA5, SCA7 and dentatorubropallidoluysian atrophy (DRPLA). Expansions of an unstable trinucleotide CAG repeat cause three of these disorders: SCA1, MJD/SCA3 and DRPLA. We studied one Brazilian family segregating an autosomal dominant type of SCA. A total of ten individuals were examined and tested for the presence of the SCA1, MJD and DRPLA mutations. Three individuals, one male and two females, were considered affected based on neurological examination; ages at onset were: 32, 36 and 41 years. The first complaint in all three patients was gait ataxia which progressed slowly over the years. Six individuals showed one allele containing an expanded CAG repeat in the SCA1 gene. The mean size of the expanded allele was 48.2 CAG units. Instability of the expanded CAG tract was seen in the two transmissions that were observed in this family. In both occasions there was a contraction of the CAG tract. Our study demonstrates that SCA1 occurs in the Brazilian population. In addition, our results stress the importance of molecular studies in the confirmation of diagnosis and for pre-symptomatic testing in SCAs.
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6

Venkataraman, Abinaya Priya, Josefine Andersson, Lina Fivelsdal, Maria Nilsson, and Alberto Domínguez-Vicent. "Impact of optical coherence tomography scan direction on the reliability of peripapillary retinal nerve fiber layer measurements." PLOS ONE 16, no. 2 (February 22, 2021): e0247670. http://dx.doi.org/10.1371/journal.pone.0247670.

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Purpose To evaluate the intradevice repeatability and agreement for peripapillary retinal nerve fiber layer (pRNFL) measurements in healthy eyes with two different scan directions and two different number of B scans. Methods pRNFL was measured with a spectral domain optical coherence tomography on 54 healthy participants. Three-dimensional optic disc scans (6 mm x 6 mm) were performed on the right eye of the participants. Two repeated scans were performed in four different settings: H1: Horizontal scan with 512 A-scans x 96 B-scans; H2: Horizontal scan with 512 A-scans x 128 B-scans; V1: Vertical scan with 512 A-scans x 96 B-scans; V2: Vertical scan with 512 A-scans x 128 B-scans. The pRNFL thickness was evaluated in twelve clock-hour sector in a circle of 3.45 mm diameter centred at the optic disc. Repeatability and agreement were assessed with within subject standard deviation (Sw) and Bland-Altman test respectively. Results The repeatability of pRNFL measurements varied depending on the scan direction and sectors. The repeatability for the horizontal sectors were better with H1 and H2, with sector 9 having the best Sw (< 3 μm). The repeatability for the vertical sectors were better with V1 and V2 with sector 5 and 9 having the best Sw (< 4 μm). The repeatability with vertical scan was more symmetric among the sectors than with horizontal scans. The repeatability metrics of the sectors did not vary much between H1 and H2 (difference < 2 μm) and between V1 and V2 (difference < 3.2 μm). Comparing horizontal and vertical scans, the vertical sectors had larger limits of agreement of about 45 μm. Conclusion The reliability of the pRNFL thickness measurements is dependent on the direction of the scan and independent on the numbers of B-scans. Vertical scans for pRNFL gives more homogeneous repeatability across the different sectors.
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7

Leiva-Gea, Isabel, Maria F. Martos-Lirio, Ana Gómez-Perea, Ana-Belen Ariza-Jiménez, Leopoldo Tapia-Ceballos, Jose Manuel Jiménez-Hinojosa, and Juan Pedro Lopez-Siguero. "Metabolic Control of the FreeStyle Libre System in the Pediatric Population with Type 1 Diabetes Dependent on Sensor Adherence." Journal of Clinical Medicine 11, no. 2 (January 6, 2022): 286. http://dx.doi.org/10.3390/jcm11020286.

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Aims: To evaluate the relationship between daily sensor scan rates and changes in HbA1c and hypoglycemia in children. Methods: We enrolled 145 paediatric T1D patients into a prospective, interventional study of the impact of the FreeStyle Libre 1 system on measures of glycemic control. Results: HbA1c was higher at lower scan rates, and decreased as the scan rate increased to 15–20 scans, after which it rose at higher scan rates. An analysis of the change in hypoglycemia, based on the number of daily sensor scans, showed there was a significant correlation between daily scan rates and hypoglycemia. Subjects with higher daily scan rates reduced all levels of hypoglycaemia. Conclusions: HbA1c is higher at lower scan rates, and decreases as scan rate increases. Reductions in hypoglycemia were evident in subjects with higher daily scan rates.
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8

Filotheou, Alexandros. "Correspondenceless scan-to-map-scan matching of homoriented 2D scans for mobile robot localisation." Robotics and Autonomous Systems 149 (March 2022): 103957. http://dx.doi.org/10.1016/j.robot.2021.103957.

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9

Peate, Ian. "Tests, scans and investigations, 8: CT scan." British Journal of Healthcare Assistants 11, no. 3 (March 2, 2017): 117–21. http://dx.doi.org/10.12968/bjha.2017.11.3.117.

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10

Moro, Adriana, Renato Puppi Munhoz, Walter Oleschko Arruda, Salmo Raskin, and Hélio Afonso Ghizoni Teive. "Clinical relevance of "bulging eyes" for the differential diagnosis of spinocerebellar ataxias." Arquivos de Neuro-Psiquiatria 71, no. 7 (July 2013): 428–30. http://dx.doi.org/10.1590/0004-282x20130056.

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ObjectiveTo investigate the relevance of the clinical finding of bulging eyes (BE) in a large Brazilian cohort of spinocerebellar ataxias (SCA), to assess its importance in clinical differential diagnosis among SCA.MethodsThree hundred sixty-nine patients from 168 Brazilian families with SCA were assessed with neurological examination and molecular genetic testing. BE was characterized by the presence of eyelid retraction. Genetically ascertained SCA3 was detected in 167 patients, SCA10 in 68 patients, SCA2 in 20, SCA1 in 9, SCA7 in 6, and SCA6 in 3 patients.ResultsBE was detected in 123 patients with SCA (33.3%), namely 109 of the 167 SCA3 patients (65.3%) and in 5 of the others SCA patients (1 SCA10 patient, 2 SCA1 patients and 2 SCA2 patients).ConclusionBE was detected in the majority of patients with SCA3 (65.3%) and could be used with a clinical tool for the differential diagnosis of SCA.
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11

Lops, M., and M. Orsini. "Scan-by-scan averaging CFAR." IEE Proceedings F Radar and Signal Processing 136, no. 6 (1989): 249. http://dx.doi.org/10.1049/ip-f-2.1989.0038.

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12

Durr, Alexandra, Giovanni Stevanin, Geraldine Cancel, Olivier Didierjean, and Alexis Brice. "Phenotype-genotype correlations in SCA1, SCA2, SCA3/MJD and SCA6." Neuromuscular Disorders 7, no. 6-7 (September 1997): 469. http://dx.doi.org/10.1016/s0960-8966(97)87331-2.

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13

Ning, Yangmin M., Clara Chen, Virginia Ellen Maher, James Xunhai Xu, Geoffrey Kim, and Richard Pazdur. "Tumor progression versus bone scan “flare” in new lesions detected on early bone scans in patients with chemo-naïve metastatic castration resistant prostate cancer (mCRPC) treated with placebo or enzalutamide." Journal of Clinical Oncology 34, no. 2_suppl (January 10, 2016): 305. http://dx.doi.org/10.1200/jco.2016.34.2_suppl.305.

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305 Background: To differentiate between bone metastasis progression vs. Tc99m scan “flare” in new lesions on early bone scans ( ≤ 12 wks), ≥ 2 additional lesions on a confirmatory scan (6 wks later) are proposed. This reduces the risk of misreading scan “flare” as progression in responding patients (pts). Independent central review (ICR) of scans from placebo (PLC)-controlled trials can help evaluate the role of confirmatory scans as PLC should neither delay progression nor elicit scan “flare”. Methods: The ICR datasets from a randomized PLC-controlled trial of enzalutamide (ENZ) in pts with chemo-naïve mCRPC were examined. Pts with ≥ 2 new lesions on Week 9 bone scans who underwent confirmatory scans were analyzed. Scan “flare” was defined as unconfirmed progression associated with responses in PSA ( ≥ 50% decline). Results: Summarized in the table. Confirmed progression on Week 9 bone scans occurred more in pts on PLC than in pts on ENZ (57% vs. 14%). In pts with unconfirmed progression, scan “flare” occurred in 80% of pts on ENZ. Of the pts with unconfirmed progression who had PSA progression, nearly 60% progressed on follow-up scans. Conclusions: The findings from this large PLC-controlled trial provide strong evidence for performing confirmatory bone scans to verify tumor progression in new lesions on early bone scans in mCRPC. For pts with unconfirmed progression, early PSA progression appears associated with progression on follow-up scans. [Table: see text]
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14

Chen, Xu, Tengfei Guo, Yubin Hou, Jing Zhang, Wenjie Meng, and Qingyou Lu. "A High Rigidity and Precision Scanning Tunneling Microscope with Decoupled XY and Z Scans." Scanning 2017 (2017): 1–7. http://dx.doi.org/10.1155/2017/1020476.

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A new scan-head structure for the scanning tunneling microscope (STM) is proposed, featuring high scan precision and rigidity. The core structure consists of a piezoelectric tube scanner of quadrant type (for XY scans) coaxially housed in a piezoelectric tube with single inner and outer electrodes (for Z scan). They are fixed at one end (called common end). A hollow tantalum shaft is coaxially housed in the XY-scan tube and they are mutually fixed at both ends. When the XY scanner scans, its free end will bring the shaft to scan and the tip which is coaxially inserted in the shaft at the common end will scan a smaller area if the tip protrudes short enough from the common end. The decoupled XY and Z scans are desired for less image distortion and the mechanically reduced scan range has the superiority of reducing the impact of the background electronic noise on the scanner and enhancing the tip positioning precision. High quality atomic resolution images are also shown.
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15

Joshi, Janhavi P., John R. Ballard, George A. Rinard, Richard W. Quine, Sandra S. Eaton, and Gareth R. Eaton. "Rapid-scan EPR with triangular scans and fourier deconvolution to recover the slow-scan spectrum." Journal of Magnetic Resonance 175, no. 1 (July 2005): 44–51. http://dx.doi.org/10.1016/j.jmr.2005.03.013.

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16

Yin, Zhye, Bruno De Man, and Jed Pack. "3D Analytic Cone-Beam Reconstruction for Multiaxial CT Acquisitions." International Journal of Biomedical Imaging 2009 (2009): 1–11. http://dx.doi.org/10.1155/2009/538389.

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A conventional 3rd generation Computed Tomography (CT) system with a single circular source trajectory is limited in terms of longitudinal scan coverage since extending the scan coverage beyond 40 mm results in significant cone-beam artifacts. A multiaxial CT acquisition is achieved by combining multiple sequential 3rd generation axial scans or by performing a single axial multisource CT scan with multiple longitudinally offset sources. Data from multiple axial scans or multiple sources provide complementary information. For full-scan acquisitions, we present a window-based 3D analytic cone-beam reconstruction algorithm by tessellating data from neighboring axial datasets. We also show that multi-axial CT acquisition can extend the axial scan coverage while minimizing cone-beam artifacts. For half-scan acquisitions, one cannot take advantage of conjugate rays. We propose a cone-angle dependent weighting approach to combine multi-axial half-scan data. We compute the relative contribution from each axial dataset to each voxel based on the X-ray beam collimation, the respective cone-angles, and the spacing between the axial scans. We present numerical experiments to demonstrate that the proposed techniques successfully reduce cone-beam artifacts at very large volumetric coverage.
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17

Mead, G. M., G. J. Rustin, S. P. Stenning, P. Vasey, N. Aass, R. Huddart, M. Sokal, and S. Kirk. "Medical Research Council trial of 2 versus 5 CT scans in the surveillance of patients with stage I non-seminomatous germ cell tumours of the testis." Journal of Clinical Oncology 24, no. 18_suppl (June 20, 2006): 4519. http://dx.doi.org/10.1200/jco.2006.24.18_suppl.4519.

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4519 Background: Surveillance is a standard management approach for stage 1 non seminomatous germ cell tumours (NSGCT), yet there is no agreement on the number of CT scans that are required to detect relapses. A randomised trial of 2 versus 5 CT scans was performed to determine whether the number of scans influenced the prognostic group (J Clin Oncol 15:594–603, 1997) at relapse. Methods: Patients with clinical stage 1 NSGCT opting for surveillance were randomised to chest and abdominal CT scans at either 3 and 12 or 3, 6, 9, 12, and 24 months, with all other investigations (clinical exams, markers, chest X-rays) carried out at equal frequency in the two arms. 3/5 patients were allocated to the 2 scan schedule. 400 patients were required to exclude a 3% increase in the proportion of patients relapsing with IGCCCG intermediate or poor prognosis disease with 90% power at the 5% significance level (1-sided). Results: 247 patients were allocated to 2 CT scans and 167 to 5 CT scans. With a median follow up of 40 months 37 (15%) relapses have occurred in the 2 scan arm and 33 (20%) in the 5 scan arm. No patients were poor prognosis at relapse but 2 (0.8%) of those relapsing in the 2 scan arm were intermediate prognosis compared to 1 (0.6%) in the 5 scan arm a difference of 0.2% (90% CI −1.2%, +1.6%). The mean diameter of abdominal mass at relapse was 2.1 cm in the two scan arm and 2.2 cm in the five scan arm. After chemotherapy a residual mass was present in 35% in the 2 scan and 36% in the 5 scan arm. No deaths have been reported. Conclusions: This study can exclude with 95% probability an increase in the proportion of patients relapsing with intermediate or poor prognosis disease of more than 1.6% if they have 2 rather than 5 CT scans as part of their surveillance protocol. CT scans at 3 and 12 months after orchidectomy should be considered as the new standard and will be associated with a reduction in radiation exposure. No significant financial relationships to disclose.
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18

Lim, Hyung Bin, Tae Seen Kang, Yeo Kyoung Won, and Jung Yeul Kim. "The Difference in Repeatability of Automated Superficial Retinal Vessel Density according to the Measurement Area Using OCT Angiography." Journal of Ophthalmology 2020 (April 17, 2020): 1–9. http://dx.doi.org/10.1155/2020/5686894.

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Purpose. To evaluate the difference in the repeatability of automated superficial retinal vessel density and foveal avascular zone (FAZ) metrics according to the measurement area of optical coherence tomography angiography (OCTA). Methods. A total of 127 normal eyes from 127 healthy subjects were included. Macular angiography images were acquired from all subjects using the Zeiss Cirrus 5000 with AngioPlex™ OCTA software. Scans of 3 × 3 mm and 6 × 6 mm were each performed twice in a randomly arranged sequence. Vessel density (VD), perfusion density (PD), and FAZ metrics of the superficial capillary plexus were calculated automatically for all scans, and the repeatabilities for both scan patterns were assessed based on intraclass correlation (ICC), coefficient of variation (CV), and coefficient of repeatability (CR) parameters. The average measured values in the two scan patterns were also compared. Results. VD was significantly greater in the 3 × 3 mm scan than in the 6 × 6 mm scan according to all parameters, whereas PD was significantly less in the 3 × 3 mm scan than in the 6 × 6 mm scan. The ICCs for VDs in the central fovea were 0.826 and 0.741 for the 3 × 3 and 6 × 6 mm scans, respectively, and the CVs were 8.00% and 12.75%. For PDs, the ICCs were 0.839 and 0.762 and the CVs were 9.32% and 14.90%. The FAZ metrics in the 3 × 3 mm scan showed good repeatability with an ICC >0.75 and a CV <10.0%. However, all ICCs for the 6 × 6 mm scans were <0.75, and the CVs were all >10%. Conclusions. The 6 × 6 mm macular angiography scans resulted in lower repeatabilities than the 3 × 3 mm scans according to all OCTA parameters, particularly in the central fovea and FAZ metrics. The 3 × 3 mm scan was more suitable than the 6 × 6 mm scan for analyzing macular microvascular density and FAZ metrics.
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19

Kollias, Pavlos, Nitin Bharadwaj, Kevin Widener, Ieng Jo, and Karen Johnson. "Scanning ARM Cloud Radars. Part I: Operational Sampling Strategies." Journal of Atmospheric and Oceanic Technology 31, no. 3 (March 1, 2014): 569–82. http://dx.doi.org/10.1175/jtech-d-13-00044.1.

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Abstract The acquisition of scanning cloud radars by the Atmospheric Radiation Measurement (ARM) program and research institutions around the world generates the need for developing operational scan strategies for cloud radars. Here, the first generation of sampling strategies for the scanning ARM cloud radars (SACRs) is presented. These scan strategies are designed to address the scientific objectives of ARM; however, they introduce an initial framework for operational scanning cloud radars. While the weather community uses scan strategies that are based on a sequence of scans at constant elevations, the SACR scan strategies are based on a sequence of scans at constant azimuth. This is attributed to the cloud geometrical properties, which are vastly different from the rain and snow shafts that are the primary targets of precipitation radars; the need to cover the cone of silence; and the scanning limitations of the SACRs. A “cloud surveillance” scan strategy is introduced that is based on a sequence of horizon-to-horizon range–height indicator (RHI) scans that sample the hemispherical sky (HS) every 30° azimuth (HSRHI). The HSRHI scan strategy is complimented with a low-elevation plan position indicator (PPI) scan. The HSRHI and PPI are repeated every 30 min to provide a static view of the cloud conditions around the SACR location. Between the HSRHI and PPI scan strategies, other scan strategies are introduced depending on the cloud conditions. In the future, information about the atmospheric cloud state will be used in a closed-loop process to optimize the selection of the SACR scan strategy.
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20

King, Kenneth. "Scan." Performing Arts Journal 17, no. 2/3 (May 1995): 100. http://dx.doi.org/10.2307/3245782.

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21

Davison, Betsy. "SCAN." Social Studies 78, no. 1 (January 1987): 42–43. http://dx.doi.org/10.1080/00220973.1944.11019822.

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22

Shiokawa, Hiroaki, Yasuhiro Fujiwara, and Makoto Onizuka. "SCAN++." Proceedings of the VLDB Endowment 8, no. 11 (July 2015): 1178–89. http://dx.doi.org/10.14778/2809974.2809980.

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23

Maag, Balz, Zimu Zhou, Olga Saukh, and Lothar Thiele. "SCAN." Proceedings of the ACM on Interactive, Mobile, Wearable and Ubiquitous Technologies 1, no. 2 (June 30, 2017): 1–21. http://dx.doi.org/10.1145/3090084.

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24

Simon, Rebecca. "SCAN:." Serials Librarian 28, no. 1-2 (April 22, 1996): 123–28. http://dx.doi.org/10.1300/j123v28n01_13.

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Narayanan, K. G. "Scan." IETE Technical Review 10, no. 1 (January 1993): 2. http://dx.doi.org/10.1080/02564602.1993.11437279.

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Narayanan, K. G. "Scan." IETE Technical Review 10, no. 6 (November 1993): 534. http://dx.doi.org/10.1080/02564602.1993.11437386.

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Narayanan, K. G. "Scan." IETE Technical Review 11, no. 2-3 (March 1994): 90. http://dx.doi.org/10.1080/02564602.1994.11437432.

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Narayanan, K. G. "Scan." IETE Technical Review 11, no. 4 (July 1994): 190. http://dx.doi.org/10.1080/02564602.1994.11437457.

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Narayanan, K. G. "Scan." IETE Technical Review 11, no. 5-6 (September 1994): 278. http://dx.doi.org/10.1080/02564602.1994.11437476.

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Narayanan, K. G. "Scan." IETE Technical Review 12, no. 1 (January 1995): 2. http://dx.doi.org/10.1080/02564602.1995.11416491.

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Narayanan, K. G. "Scan." IETE Technical Review 12, no. 2 (March 1995): 92. http://dx.doi.org/10.1080/02564602.1995.11416512.

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Narayanan, K. G. "Scan." IETE Technical Review 12, no. 3 (May 1995): 174. http://dx.doi.org/10.1080/02564602.1995.11416524.

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Narayanan, K. G. "Scan." IETE Technical Review 12, no. 5-6 (September 1995): 308. http://dx.doi.org/10.1080/02564602.1995.11416546.

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Narayanan, K. G. "Scan." IETE Technical Review 13, no. 1 (January 1996): 2. http://dx.doi.org/10.1080/02564602.1996.11416567.

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Narayanan, K. G. "Scan." IETE Technical Review 13, no. 2 (March 1996): 70. http://dx.doi.org/10.1080/02564602.1996.11416582.

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Narayanan, K. G. "Scan." IETE Technical Review 13, no. 3 (May 1996): 134. http://dx.doi.org/10.1080/02564602.1996.11416596.

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Singh, Y. P. "Scan." IETE Technical Review 13, no. 6 (November 1996): 287. http://dx.doi.org/10.1080/02564602.1996.11416620.

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Singh, Y. P. "Scan." IETE Technical Review 14, no. 4-5 (July 1997): 230. http://dx.doi.org/10.1080/02564602.1997.11416680.

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Singh, Y. P. "Scan." IETE Technical Review 15, no. 5 (September 1998): 304. http://dx.doi.org/10.1080/02564602.1998.11416764.

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40

Krishna, Vinod. "Scan." IETE Technical Review 16, no. 3-4 (May 1999): 270. http://dx.doi.org/10.1080/02564602.1999.11416840.

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Sahay, Dilip. "Scan." IETE Technical Review 19, no. 3 (May 2002): 94. http://dx.doi.org/10.1080/02564602.2002.11417017.

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Sahay, Dilip. "Scan." IETE Technical Review 19, no. 6 (November 2002): 350. http://dx.doi.org/10.1080/02564602.2002.11417049.

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Sahay, Dalip. "Scan." IETE Technical Review 20, no. 1 (January 2003): 2. http://dx.doi.org/10.1080/02564602.2003.11417062.

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44

Sahay, Dilip. "Scan." IETE Technical Review 20, no. 6 (November 2003): 480. http://dx.doi.org/10.1080/02564602.2003.11417107.

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45

Sahay, Dilip. "Scan." IETE Technical Review 21, no. 1 (January 2004): 2. http://dx.doi.org/10.1080/02564602.2004.11417121.

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46

Sahay, Dilip. "Scan." IETE Technical Review 21, no. 2 (March 2004): 100. http://dx.doi.org/10.1080/02564602.2004.11417135.

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47

Sahay, Dilip. "Scan." IETE Technical Review 21, no. 3 (May 2004): 180. http://dx.doi.org/10.1080/02564602.2004.11417143.

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48

Sahay, Dilip. "Scan." IETE Technical Review 21, no. 4 (July 2004): 230. http://dx.doi.org/10.1080/02564602.2004.11417149.

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49

Sahay, Dilip. "Scan." IETE Technical Review 21, no. 6 (November 2004): 370. http://dx.doi.org/10.1080/02564602.2004.11417165.

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50

Sahay, Dilip. "Scan." IETE Technical Review 22, no. 3 (May 2005): 172. http://dx.doi.org/10.1080/02564602.2005.11657898.

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