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Статті в журналах з теми "Subsequent analysis"

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Subsequent analysis.

Автор: Grafiati

Опубліковано: 30 травня 2022

Оновлено: 31 травня 2022

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1

Fitzmaurice, Malgosia. "Subsequent Agreement and Subsequent Practice." International Community Law Review 22, no. 1 (March 4, 2020): 14–32. http://dx.doi.org/10.1163/18719732-12341419.

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Abstract This article is devoted to the analysis of the 13 Draft Conclusions on Subsequent Agreement and Subsequent Practice in relation to the Interpretation of Treaties (with commentaries) (the ‘Draft Conclusions’) adopted in 2018 by the International Law Commission (the ‘ILC’), as well as presenting some reactions to the Draft Conclusions. It provides some reflections on the monumental contribution that the ICL and the Special Rapporteur’s have made on this project, and the importance of this achievement for practitioners.

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2

Greig, Anthony C. "Fundamental analysis and subsequent stock returns." Journal of Accounting and Economics 15, no. 2-3 (June 1992): 413–42. http://dx.doi.org/10.1016/0165-4101(92)90026-x.

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3

Hong, Soon Oh, Min Ho Kong, Se Youn Jang, Jung Hee Kim, Yoon Ha, Dong Soo Kang, and Kwan Young Song. "Analysis of Subsequent Fractures after Percutaneous Vertebroplasty." Asian Journal of Pain 2, no. 1 (April 30, 2016): 15–21. http://dx.doi.org/10.35353/ajp.2.1.15.

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4

Chiang, Yuan-Cheng, Fu-Chan Wei, and Lian-May Chen. "Heel Replantation and Subsequent Analysis of Gait." Plastic and Reconstructive Surgery 91, no. 4 (April 1993): 729–33. http://dx.doi.org/10.1097/00006534-199304000-00029.

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5

Petersen, Janne, Karen Bandeen-Roche, Esben Budtz-Jørgensen, and Klaus Groes Larsen. "Predicting Latent Class Scores for Subsequent Analysis." Psychometrika 77, no. 2 (February 7, 2012): 244–62. http://dx.doi.org/10.1007/s11336-012-9248-6.

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6

Longland, A. C., C. Barfoot, and P. A. Harris. "Insulin Resistance – Hay Analysis and Subsequent Feeding Management." Journal of Equine Veterinary Science 30, no. 2 (February 2010): 110. http://dx.doi.org/10.1016/j.jevs.2010.01.032.

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7

Tuomivaara, Leena. "An analysis of etiological risk factors and subsequent fertility." Acta Obstetricia et Gynecologica Scandinavica 70, no. 7-8 (January 1991): 635–36. http://dx.doi.org/10.3109/00016349109007934.

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8

Schubert, Matthew M., Ben Desbrow, Surendran Sabapathy, and Michael Leveritt. "Acute exercise and subsequent energy intake. A meta-analysis." Appetite 63 (April 2013): 92–104. http://dx.doi.org/10.1016/j.appet.2012.12.010.

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9

Tomanec, Filip, Sona Rusnakova, Jiri Kohut, and Martina Kalova. "Composite External Fixators: Design with Subsequent FEM Analysis Optimization." Manufacturing Technology 19, no. 3 (June 1, 2019): 513–17. http://dx.doi.org/10.21062/ujep/321.2019/a/1213-2489/mt/19/3/513.

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10

Daulet, G., G. Atanbaeva, S. Tuleukhanov, A. Ydyrys, A. Baishanbo, and S. Abdireshov. "Injection of sorbent and subsequent analysis of blood cells." International Journal of Biology and Chemistry 11, no. 1 (2018): 82–88. http://dx.doi.org/10.26577/ijbch-2018-1-316.

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11

Laux, Dale L. "Effects of Luminol on the Subsequent Analysis of Bloodstains." Journal of Forensic Sciences 36, no. 5 (September 1, 1991): 13171J. http://dx.doi.org/10.1520/jfs13171j.

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12

Oerlemans, Marjolein EJ, Marjan van den Akker, Agnes G. Schuurman, Eliane Kellen, and Frank Buntinx. "A meta-analysis on depression and subsequent cancer risk." Clinical Practice and Epidemiology in Mental Health 3, no. 1 (2007): 29. http://dx.doi.org/10.1186/1745-0179-3-29.

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13

Morgenroth, Konstanze, and Dieter Boss. "Design of eCRFs in consideration of subsequent data analysis." Pharmaceutical Programming 1, no. 2 (December 2008): 92–96. http://dx.doi.org/10.1179/175709206x372290.

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14

Mueller, Tim, and Neil Burns. "Analysis and Subsequent Testing of Cracked Brass Connector Housings." Journal of Failure Analysis and Prevention 9, no. 5 (July 28, 2009): 466–69. http://dx.doi.org/10.1007/s11668-009-9278-2.

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15

Sun, Gang, Hai Tang, Min Li, Xunwei Liu, Peng Jin, and Li Li. "Analysis of risk factors of subsequent fractures after vertebroplasty." European Spine Journal 23, no. 6 (November 20, 2013): 1339–45. http://dx.doi.org/10.1007/s00586-013-3110-0.

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16

Weber, Thomas, Dietrich Stoyan, and Mari Myllymäki. "Statistical analysis of associations between subsequent prehistoric settlement patterns." Journal of Archaeological Science: Reports 9 (October 2016): 330–39. http://dx.doi.org/10.1016/j.jasrep.2016.07.022.

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17

Eldridge, Ronald C., Michael Pawlita, Lauren Wilson, Philip E. Castle, Tim Waterboer, Patti E. Gravitt, Mark Schiffman, and Nicolas Wentzensen. "Smoking and subsequent human papillomavirus infection: a mediation analysis." Annals of Epidemiology 27, no. 11 (November 2017): 724–30. http://dx.doi.org/10.1016/j.annepidem.2017.10.004.

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18

Mu, Min, Su-Fang Wang, Jie Sheng, Yan Zhao, Hu-Zhong Li, Chuan-Lai Hu, and Fang-Biao Tao. "Birth weight and subsequent blood pressure: A meta-analysis." Archives of Cardiovascular Diseases 105, no. 2 (February 2012): 99–113. http://dx.doi.org/10.1016/j.acvd.2011.10.006.

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19

Sweis, Randy F., Michael W. Drazer, and Mark J. Ratain. "Analysis of Impact of Post-Treatment Biopsies in Phase I Clinical Trials." Journal of Clinical Oncology 34, no. 4 (February 1, 2016): 369–74. http://dx.doi.org/10.1200/jco.2015.63.6126.

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Анотація:

Purpose The use of biopsy-derived pharmacodynamic biomarkers is increasing in early-phase clinical trials. It remains unknown whether drug development is accelerated or enhanced by their use. We examined the impact of biopsy-derived pharmacodynamic biomarkers on subsequent drug development through a comprehensive analysis of phase I oncology studies from 2003 to 2010 and subsequent publications citing the original trials. Methods We conducted a search to identify and examine publications of phase I oncology studies including the use of biopsy-derived pharmacodynamic biomarkers between 2003 and 2010. Characteristics of those studies were extracted and analyzed, along with outcomes from the biomarker data. We then compiled and reviewed publications of subsequent phase II and III trials citing the original phase I biomarker studies to determine the impact on drug development. Results We identified 4,840 phase I oncology publications between 2003 and 2010. Seventy-two studies included a biopsy-derived pharmacodynamic biomarker. The proportion of biomarker studies including nondiagnostic biopsies increased over time (P = .002). A minimum of 1,873 tumor biopsies were documented in the 72 studies, 12 of which reported a statistically significant biomarker result. Thirty-three percent of studies (n = 24) were referenced by subsequent publications specifically with regard to the biomarkers. Only five positive biomarker studies were cited subsequently, and maximum tolerated dose was used for subsequent drug development in all cases. Conclusion Despite their increased use, the impact of biopsy-derived pharmacodynamic biomarkers in phase I oncology studies on subsequent drug development remains uncertain. No impact on subsequent dose or schedule was demonstrated. This issue requires further evaluation, given the risk and cost of such studies.

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20

Dunkel, I. J., A. Kosack, E. Riedel, T. E. Kiehn, T. N. Small, and L. H. Wexler. "Vancomycin-resistant enterococcus (VRE) in pediatric oncology patients: An analysis of potential consequences of colonization and infection." Journal of Clinical Oncology 25, no. 18_suppl (June 20, 2007): 9537. http://dx.doi.org/10.1200/jco.2007.25.18_suppl.9537.

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9537 Background: VRE colonization and infection have emerged as an issue for pediatric oncology patients, but little is known about the long-term risks following initial VRE positivity in this population. The purpose of this study was to determine the risk of subsequent VRE infection in colonized or infected pediatric oncology patients and to try to identify risk factors. Methods: A retrospective analysis was performed of the 57 pediatric oncology patients who had a positive VRE culture at MSKCC from 1996–2000 and subsequently received chemotherapy and/or radiation therapy. Patients whose only subsequent treatment was allogeneic stem cell transplantation were excluded. The incidence of subsequent VRE infection was calculated using a competing risk analysis accounting for death from non-VRE causes as a competing risk. Data regarding hypothesized risk factors for subsequent VRE infections were collected. Results: Ten of the 57 patients had subsequent VRE infection, but none was the primary cause of death. The cumulative incidence of subsequent infection was 14% (7–27%, 95% confidence interval) at 1 year and 16% (9–29%, 95% confidence interval) at 2 years. Eight developed their subsequent infection within 3 months; the other 2 occurred at 15 and 30 months. A formal analysis of risk factors was not attempted due to the small number of events; however, none of the hypothesized risk factors (initial VRE colonization versus infection, number of chemotherapy or radiation therapy regimens, number of neutropenic or mucositis episodes, number of hospitalizations, number of abdominal surgeries or stem cell transplantations) appeared to differ between those who developed a subsequent infection and those who did not. Conclusions: Pediatric oncology patients with VRE colonization or initial infection are at risk for subsequent VRE infection, particularly within the first 3 months of initial diagnosis of VRE positivity. No significant financial relationships to disclose.

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21

Khamenehfar, Avid, and Paul C.H. Li. "Microfluidic Devices for Circulating Tumor Cells Isolation and Subsequent Analysis." Current Pharmaceutical Biotechnology 17, no. 9 (June 6, 2016): 810–21. http://dx.doi.org/10.2174/1389201017666160301103509.

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22

Herrmann, C. S., T. Arnold, A. Visbeck, H. P. Hundemer, and H. C. Hopf. "Adaptive frequency decomposition of EEG with subsequent expert system analysis." Computers in Biology and Medicine 31, no. 6 (November 2001): 407–27. http://dx.doi.org/10.1016/s0010-4825(01)00017-8.

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23

Zhang, Quiyang, and T. R. Tiersch. "Cryopreservation of leucocytes of channel catfish for subsequent cytogenetic analysis." Journal of Fish Biology 47, no. 6 (December 1995): 1016–25. http://dx.doi.org/10.1111/j.1095-8649.1995.tb06025.x.

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24

Lv, Mengmeng, Xingya Zhu, Shanliang Zhong, Weixian Chen, Qing Hu, Tengfei Ma, Jun Zhang, Xiaohui Zhang, Jinhai Tang, and Jianhua Zhao. "Radial Scars and Subsequent Breast Cancer Risk: A Meta-Analysis." PLoS ONE 9, no. 7 (July 14, 2014): e102503. http://dx.doi.org/10.1371/journal.pone.0102503.

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25

Liang, Ji-An, Li-Min Sun, Chih-Hsin Muo, Fung-Chang Sung, Shih-Ni Chang, and Chia-Hung Kao. "The Analysis of Depression and Subsequent Cancer Risk in Taiwan." Cancer Epidemiology Biomarkers & Prevention 20, no. 3 (February 4, 2011): 473–75. http://dx.doi.org/10.1158/1055-9965.epi-10-1280.

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26

Kanis, J. A., O. Johnell, C. De Laet, H. Johansson, A. Oden, P. Delmas, J. Eisman, et al. "A meta-analysis of previous fracture and subsequent fracture risk." Bone 35, no. 2 (August 2004): 375–82. http://dx.doi.org/10.1016/j.bone.2004.03.024.

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27

Jing, Zhaoqian, Shiwei Cao, Ting Yu, and Jing Hu. "Degradation Characteristics of Aniline with Ozonation and Subsequent Treatment Analysis." Journal of Chemistry 2015 (2015): 1–6. http://dx.doi.org/10.1155/2015/905921.

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Owing to the toxicity and low biodegradability of aniline in water, its removal usually needs high cost processes such as adsorption and advanced oxidation. The degradation characteristics of aniline during ozonation were studied. The influence of operation parameters such as contact time, initial concentration, ozone dosage, temperature, and pH was also investigated. With ozone dosage of 22 mg/L, neutral pH, and room temperature, the ozonation removed aniline efficiently. After two hours’ ozonation, aniline removal reached 93.57%, and the corresponding COD removal was 31.03%, which indicated most of aniline was transformed into intermediates. At alkaline conditions, the aniline was more susceptible to being removed by ozonation owing to more hydroxyl radicals’ production. The results of GC-MS indicated many intermediates appeared during the process of ozonation such as butane diacid, oxalic acid, and formic acid. The intermediates produced during ozonation were more biodegradable than aniline; thus the ozonation of such organic compounds as aniline could be integrated with biological processes for further removal.

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28

Naya, Masanao, and Nagara Tamaki. "Stress MPI, coronary CTA, and multimodality for subsequent risk analysis." Journal of Nuclear Cardiology 23, no. 2 (January 21, 2016): 198–201. http://dx.doi.org/10.1007/s12350-016-0400-z.

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29

Smith, S. H., and L. T. Taylor. "Extraction of various additives from polystyrene and their subsequent analysis." Chromatographia 56, no. 3-4 (August 2002): 165–69. http://dx.doi.org/10.1007/bf02493206.

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30

Check, J. H., K. Nowroozi, C. H. Wu, and A. Bollendorf. "Correlation of Semen Analysis and Hypoosmotic Swelling Test with Subsequent Pregnancies." Archives of Andrology 20, no. 3 (January 1988): 257–60. http://dx.doi.org/10.3109/01485018808987081.

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31

Sorensen, Jonathan, Heidi Bonner, Shelley Visconte, Mark Vigen, and S. O. Woods. "Home Invasion Homicide Offenders: An Analysis of Subsequent Prison Rule Violations." Violence and Victims 30, no. 6 (2015): 1082–98. http://dx.doi.org/10.1891/0886-6708.vv-d-14-00043.

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This study adds to the small body of research on home invasion by describing the circumstances surrounding home invasions that resulted in the death of a resident. The 2 most common types of home invasion homicides (HIHs) involved “drug ripoffs” and robberies of older adults for money and property. The study also examined subsequent rule-violating behavior of 132 HIH inmates while incarcerated. The rate of rule violations among HIH inmates was similar to a broader cohort of incarcerated homicide offenders. A logistic regression model identified variation in assaultive prison behavior based on some routine predictors (age, education, race, and prior imprisonment) and 2 associated with the crime (method of killing and age by gender of victims).

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32

Wilke, Hans, and Lucy J. Robertson. "Preservation of Giardia cysts in stool samples for subsequent PCR analysis." Journal of Microbiological Methods 78, no. 3 (September 2009): 292–96. http://dx.doi.org/10.1016/j.mimet.2009.06.018.

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33

Arrowsmith, Peter, and Steven K. Hughes. "Entrainment and Transport of Laser Ablated Plumes for Subsequent Elemental Analysis." Applied Spectroscopy 42, no. 7 (September 1988): 1231–39. http://dx.doi.org/10.1366/0003702884430100.

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Several cell designs have been systematically evaluated for gas flow entrainment and transport of laser ablated material to a secondary excitation source for elemental analysis. The best cell is not limited to samples of particular size or shape and is insensitive to sample surface irregularity. An annular gas sheath around the cell results in a transient response sufficiently fast to permit depth and lateral sampling of single samples or rapid throughput of different samples but slow enough to give a steady signal with laser repetition rates ≥10 Hz. Entrainment and transport of ablated particulates have been investigated experimentally and by model calculation for a test material (Mo metal). The equations for predicting diffusive and gravitational loss of particles in a horizontal tube are presented and discussed. The major loss mechanism appears to be gravitational deposition of relatively large particles formed during ablation and possibly by coalescence within the transfer tube. Entrainment of ablated Mo by the cell and mass transport from the cell to the secondary source were determined to be ∼90% and ∼40% efficient, respectively. Shot-to-shot fluctuation in particle size may cause corresponding variation in transport efficiency when the upper end of the ablated particle size distribution exceeds the size limit for particle transport.

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34

Xu, Xiao-Bang, Xu Cheng, and Kim Craven. "An analysis on magnetically induced subsequent fault in utility line topologies." Electric Power Systems Research 63, no. 3 (October 2002): 161–68. http://dx.doi.org/10.1016/s0378-7796(02)00122-0.

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35

Bandaranayake, R. C., A. J. Buzzard, and V. C. Marshall. "EFFECTS OF PUBLISHING MULTIPLE-CHOICE QUESIONS ON THEIR SUBSEQUENT ITEM ANALYSIS." ANZ Journal of Surgery 60, no. 12 (December 1990): 937–41. http://dx.doi.org/10.1111/j.1445-2197.1990.tb07509.x.

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36

CHATZIPLIS, DIMITRIOS G., HENNING HAMANN, and CHRIS S. HALEY. "Selection and subsequent analysis of sib pair data for QTL detection." Genetical Research 78, no. 2 (October 2001): 177–86. http://dx.doi.org/10.1017/s0016672301005225.

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Haseman and Elston (1972) developed a robust regression method for the detection of linkage between a marker and a quantitative trait locus (QTL) using sib pair data. The principle underlying this method is that the difference in phenotypes between pairs of sibs becomes larger as they share a decreasing number of alleles at a particular QTL identical by descent (IBD) from their parents. In this case, phenotypically very different sibs will also on average share a proportion of alleles IBD at any marker linked to the QTL that is lower than the expected value of 0·5. Thus, the deviation of the proportion of marker alleles IBD from the expected value in pairs of sibs selected to be phenotypically different (i.e. discordant) can provide a test for the presence of a QTL. A simple regression method for QTL detection in sib pairs selected for high phenotypic differences is presented here. The power of the analytical method was found to be greater than the power obtained using the standard analysis when samples of sib pairs with high phenotypic differences were used. However, the use of discordant sib pairs was found to be less powerful for QTL detection than alternative selective genotyping schemes based on the phenotypic values of the sibs except with intense selection, when its advantage was only marginal. The most effective selection scheme overall was the use of sib pairs from entire families selected on the basis of high within-family variance for the trait in question. There is little effect of selection on QTL position estimates, which are in good agreement with the simulated values. However, QTL variance estimates are biased to a greater or lesser degree, depending on the selection method.

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37

Dzieżyc, Karolina, Tomasz Litwin, Grzegorz Chabik, Karolina Gramza, and Anna Członkowska. "Families with Wilson's disease in subsequent generations: Clinical and genetic analysis." Movement Disorders 29, no. 14 (October 18, 2014): 1828–32. http://dx.doi.org/10.1002/mds.26057.

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38

Grandjean, D., J. C. Beolor, M. T. Quincon, and E. Savel. "Automated Robotic Extraction and Subsequent Analysis of Diclofenac in Plasma Samples." Journal of Pharmaceutical Sciences 78, no. 3 (March 1989): 247–49. http://dx.doi.org/10.1002/jps.2600780316.

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39

Hardoby, Melissa, and Aaron Mann. "An Analysis of Health Care Disparities and Subsequent Public Policy Initiatives." Journal of Human Behavior in the Social Environment 23, no. 7 (October 2013): 824–40. http://dx.doi.org/10.1080/10911359.2013.809286.

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40

Bath, Philip M. W., and Laura J. Gray. "Association between hormone replacement therapy and subsequent stroke: a meta-analysis." BMJ 330, no. 7487 (January 7, 2005): 342. http://dx.doi.org/10.1136/bmj.38331.655347.8f.

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41

Hess, Jennifer, Alexandra Maria Walsh, and Kristian Schafernak. "Mutational analysis of radiation-induced subsequent thyroid cancers in pediatric patients." Journal of Clinical Oncology 38, no. 15_suppl (May 20, 2020): e22531-e22531. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e22531.

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e22531 Background: The genetic landscape of radiation induced pediatric thyroid cancers is unclear. Radiation (RT) induced thyroid cancers frequently demonstrate tumorigenesis driven by fusion oncogenes. However, data is limited to children exposed to radioactive contamination after the Chernobyl nuclear accident. Little is known about the genetic landscape of subsequent pediatric thyroid cancers after RT exposure for the treatment of a primary malignancy or conditioning regimens prior to bone marrow transplantation (BMT). The objective of this study was to assess the prevalence of different mutations in a small cohort of pediatric patients who developed a subsequent thyroid cancer after RT exposure for the treatment of a primary disease. Methods: This is a single-center retrospective study. Thyroid tissue blocks from 10 pediatric patients who underwent thyroidectomy between 2010 and 2019 for subsequent thyroid cancers after RT for treatment of a primary malignancy or BMT were analyzed for genetic alterations using targeted next-generation sequencing for alterations in 112 genes linked to thyroid cancer. Thyroid cancers included 7 papillary (PTC) and 3 follicular thyroid carcinomas (FTC). Results: Ten samples (6 females) were genotyped. The mean age at thyroid cancer diagnosis was 15.7 years (range 11–22 years) at a mean of 10.3 years (range 6 – 19 years) after RT exposure. The mean RT dose was 2618 cGy (range 400 – 10,080 cGy) delivered to the head, neck, and/or chest. Mutations were noted in 6/10 (60%) of patients. Mutations were detected in 6/7 (85.7%) of PTC cases: EMLA/NTRK in 2 cases, STRN/ALK in 2 cases, RET in 1 case, and CCDC30/ROS in 1 case. A DICER.1 c.5438A > C p.E1813A was also identified in a patient with an EMLA/NTRK fusion. Of 3 FTC patients, (2/3) 67% had copy number alterations, but no mutations were observed. BRAFV600E mutations were not present in any tissues analyzed. Conclusions: An exceedinlgy rare ROS fusion was identified. Multiple RT induced thyroid lesions were positive for classic therapeutic targets including NTRK3, ALK, ROS1, and RET fusions, demonstrating a potential role for tyrosine kinase inhibitor therapy for refractory, recurrent or metastatic disease. All cases were negative for mutant BRAFV600E consistent with the pathogenesis of RT induced thyroid cancers primarily activated by fusions rather than point mutations. Larger, pediatric cohorts with RT induced thyroid cancers followed long term will enable the genotypic variability, clinical presentation, and response to therapy to be better assessed.

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42

Zhang, Yantian, Alberto Goldszal, John Butman, and Peter Choyke. "Improving Image Contrast Using Principal Component Analysis for Subsequent Image Segmentation." Journal of Computer Assisted Tomography 25, no. 5 (September 2001): 817–22. http://dx.doi.org/10.1097/00004728-200109000-00024.

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43

Einarson, Thomas R., Márcio Machado, and Michiel Eric Henk Hemels. "Blood glucose and subsequent cardiovascular disease: update of a meta-analysis." Current Medical Research and Opinion 27, no. 11 (October 5, 2011): 2155–63. http://dx.doi.org/10.1185/03007995.2011.626760.

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44

Maenhaut, W., R. Hillamo, T. Mäkelä, J. L. Jaffrezo, M. H. Bergin, and C. I. Davidson. "A new cascade impactor for aerosol sampling with subsequent PIXE analysis." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 109-110 (April 1996): 482–87. http://dx.doi.org/10.1016/0168-583x(95)00955-8.

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Huang, Chiungjung. "Academic Achievement and Subsequent Depression: A Meta-analysis of Longitudinal Studies." Journal of Child and Family Studies 24, no. 2 (October 22, 2013): 434–42. http://dx.doi.org/10.1007/s10826-013-9855-6.

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Hwang, L., I. J. Boero, D. P. Triplett, R. K. Matsuno, B. Xu, E. F. Gillespie, J. P. Einck, and J. D. Murphy. "Subsequent Cancer-Directed Therapy After Radical Prostatectomy: A Population-Based Analysis." International Journal of Radiation Oncology*Biology*Physics 93, no. 3 (November 2015): E239—E240. http://dx.doi.org/10.1016/j.ijrobp.2015.07.1150.

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Khuu, Alicia, Scott Chadwick, Sébastien Moret, Xanthe Spindler, Peter Gunn, and Claude Roux. "Impact of one-step luminescent cyanoacrylate treatment on subsequent DNA analysis." Forensic Science International 286 (May 2018): 1–7. http://dx.doi.org/10.1016/j.forsciint.2018.02.015.

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TAKAGI, Hiroshi, Takahito MIKAMI, Tomoya SHIBAYAMA, Ryo MATSUMARU, Mario de LEON, Miguel ESTEBAN, Thao Danh NGUYEN, and Ryota NAKAMURA. "ANALYSIS OF THE 2013 TYPHOON YOLANDA (HAIYAN) AND SUBSEQUENT STORM SURGE." Journal of Japan Society of Civil Engineers, Ser. B3 (Ocean Engineering) 70, no. 2 (2014): I_1206—I_1211. http://dx.doi.org/10.2208/jscejoe.70.i_1206.

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