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302. Diagnosis and severity criteria for sinusoidal obstruction syndrome/veno-occlusive disease in pediatric patients: a new classification from the European society for blood and marrow transplantation

Author

Corbacioglu, S, Carreras, E, Ansari, M, Balduzzi, A, Cesaro, S, Dalle, J-H, Dignan, F, Gibson, B, Guengoer, T, Gruhn, B, Lankester, A, Locatelli, F, Pagliuca, A, Peters, C, Richardson, P G, Schulz, A S, Sedlacek, P, Stein, J, Sykora, K-W, Toporski, J, Trigoso, E, Vetteranta, K, Wachowiak, J, Wallhult, E, Wynn, R, Yaniv, I, Yesilipek, A, Mohty, M, and Bader, P

Abstract

The advances in hematopoietic cell transplantation (HCT) over the last decade have led to a transplant-related mortality below 15%. Hepatic sinusoidal obstruction syndrome/veno-occlusive disease (SOS/VOD) is a life-threatening complication of HCT that belongs to a group of diseases increasingly identified as transplant-related, systemic endothelial diseases. In most cases, SOS/VOD resolves within weeks; however, severe SOS/VOD results in multi-organ dysfunction/failure with a mortality rate >80%. A timely diagnosis of SOS/VOD is of critical importance, given the availability of therapeutic options with favorable tolerability. Current diagnostic criteria are used for adults and children. However, over the last decade it has become clear that SOS/VOD is significantly different between the age groups in terms of incidence, genetic predisposition, clinical presentation, prevention, treatment and outcome. Improved understanding of SOS/VOD and the availability of effective treatment questions the use of the Baltimore and Seattle criteria for diagnosing SOS/VOD in children. The aim of this position paper is to propose new diagnostic and severity criteria for SOS/VOD in children on behalf of the European Society for Blood and Marrow Transplantation.

Published
2018
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304. Large, deepwater slope failures: Implications for landslide-generated tsunamis

Author

Lo Iacono, C., Gracia, E., Zaniboni, F., Pagnoni, G., Tinti, S., Bartolome, R., Masson, D. G., Wynn, R. B., Lourenco, N., Pinto de Abreu, M., Danobeitia, J. J., Zitellini, N., Lo Iacono, C., Gracia, E., Zaniboni, F., Pagnoni, G., Tinti, S., Bartolome, R., Masson, D. G., Wynn, R. B., Lourenco, N., Pinto de Abreu, M., Danobeitia, J. J., and Zitellini, N.

Abstract

Deepwater landslides are often underestimated as potential tsunami triggers. The North Gorringe avalanche (NGA) is a large (∼80 km3 and 35 km runout) newly discovered and deepwater (2900 m to 5100 m depth) mass failure located at the northern flank of Gorringe Bank on the southwest Iberian margin. Steep slopes and pervasive fracturing are suggested as the main preconditioning factors for the NGA, while an earthquake is the most likely trigger mechanism. Near-field tsunami simulations show that a mass failure similar to the NGA could generate a wave >15 m high that would hit the south Portuguese coasts in ∼30 min. This suggests that deepwater landslides require more attention in geo-hazard assessment models of southern Europe, as well as, at a global scale, in seismically active margins.

Published
2012
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307. A Multicentric Comparative Analysis of Outcomes of Hla Identical Related Cord Blood and Bone Marrow Transplantation in Patients With Beta-thalassemia Or Sickle Cell Disease

Author

UCL - Cliniques universitaires Saint-Luc, UCL - MD/GYPE - Département de gynécologie, d'obstétrique et de pédiatrie, Kabbara, N., Vermylen, Christiane, Locatelli, F., Rocha, V., Grafakos, S., Ghavamzadeh, A., Roberts, I., Li, C. K., Bernaudin, F., Dalle, J. H., Stein, Jean-Louis, Wynn, R., Lutz, P., Catherine, C., Pinto, F., Angelucci, E., Socie, G., Gluckman, E., Walters, M., 14th Annual Meeting of the European-Hematology-Association, UCL - Cliniques universitaires Saint-Luc, UCL - MD/GYPE - Département de gynécologie, d'obstétrique et de pédiatrie, Kabbara, N., Vermylen, Christiane, Locatelli, F., Rocha, V., Grafakos, S., Ghavamzadeh, A., Roberts, I., Li, C. K., Bernaudin, F., Dalle, J. H., Stein, Jean-Louis, Wynn, R., Lutz, P., Catherine, C., Pinto, F., Angelucci, E., Socie, G., Gluckman, E., Walters, M., and 14th Annual Meeting of the European-Hematology-Association

Published
2009

309. A multicentric comparative analysis of outcomes of HLA identical related cord blood and bone marrow transplantation in patients with beta-thalassemia or sickle cell disease

Author

UCL - Cliniques universitaires Saint-Luc, UCL - MD/GYPE - Département de gynécologie, d'obstétrique et de pédiatrie, Kabbara, N., Vermylen, Christiane, Locatelli, F., Rocha, V., Grafakos, S., Ghavamzadeh, A., Roberts, I., Li, C. K., Bernaudin, F., Dalle, J. H., Stein, Jean-Louis, Wynn, R., Lutz, P., Cordonnier, C., Pinto, F., Angelucci, E., Socie, G., Gluckman, E., Walters, M., UCL - Cliniques universitaires Saint-Luc, UCL - MD/GYPE - Département de gynécologie, d'obstétrique et de pédiatrie, Kabbara, N., Vermylen, Christiane, Locatelli, F., Rocha, V., Grafakos, S., Ghavamzadeh, A., Roberts, I., Li, C. K., Bernaudin, F., Dalle, J. H., Stein, Jean-Louis, Wynn, R., Lutz, P., Cordonnier, C., Pinto, F., Angelucci, E., Socie, G., Gluckman, E., and Walters, M.

Published
2008

311. An overview and analysis of theories employed in telemedicine studies. A field in search of an identity.

Author

Gammon D, Johannessen LK, Sørensen T, Wynn R, Whitten P, Gammon, D, Johannessen, L K, Sørensen, T, Wynn, R, and Whitten, P

Abstract

Objectives: This study asks: What theories are employed in telemedicine studies? How might they be categorized in ways that help distinguish the knowledge base of telemedicine?Methods: Theories in use were identified from a database of telemedicine-related publications between 1990 and 2005. Eighty-three (5% of 1615) articles referred to a theoretical concept. Grounded Theory procedures were used to analyze and categorize theories, while descriptive statistics were used for supplementary information.Results: The proportion of studies with theory was 3% in 1999 and 7% in 2005. The 83 articles were dispersed among 48 of the in total 795 different journals in the original sample. Identified theories were grouped into two main categories; 'shared' (used in two or more studies) and 'lone ranger'. All of the shared theories are social science theories employed without notable adjustments to any uniquely defining features of telemedicine; diffusion, technology acceptance, health behavior, science and technology studies (STS), and economics. Theoretical concepts within the lone ranger category may well address unique features of telemedicine, but have yet to attract the attention of colleagues.Conclusion: The theories identified as 'shared' play an important role, but are inadequate in illuminating any unique features of telemedicine. The future of telemedicine as a field will need to identify its underlying theoretical components. Frameworks employed in the field of evaluation may aid in identifying the types of theories worth articulating in telemedicine. [ABSTRACT FROM AUTHOR]

Published
2008

319. Structure-based design and mechanisms of allosteric inhibitors for mitochondrial branched-chain α-ketoacid dehydrogenase kinase

Author

Tso, Shih-Chia, primary, Qi, Xiangbing, additional, Gui, Wen-Jun, additional, Chuang, Jacinta L., additional, Morlock, Lorraine K., additional, Wallace, Amy L., additional, Ahmed, Kamran, additional, Laxman, Sunil, additional, Campeau, Philippe M., additional, Lee, Brendan H., additional, Hutson, Susan M., additional, Tu, Benjamin P., additional, Williams, Noelle S., additional, Tambar, Uttam K., additional, Wynn, R. Max, additional, and Chuang, David T., additional

Published
2013
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321. Catabolic Defect of Branched-Chain Amino Acids Promotes Heart Failure.

Author

Haipeng Sun, Olson, Kristine C., Chen Gao, Prosdocimo, Domenick A., Meiyi Zhou, Zhihua Wang, Jeyaraj, Darwin, Ji-Youn Youn, Shuxun Ren, Yunxia Liu, Rau, Christoph D., Shah, Svati, Ilkayeva, Olga, Wen-Jun Gui, William, Noelle S., Wynn, R. Max, Newgard, Christopher B., Hua Cai, Xinshu Xiao, and Chuang, David T.

Published
2016
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322. KINEMATIC-WAVE MODEL IN THE REAL-TIME SOLUTION OF THE INVERSE FURROW IRRIGATION PROBLEM

Author

Wynn R. Walker, Gary P. Merkley, and Carlos Alberto Vieira de Azevedo

Subjects
irrigation management, Environmental Engineering, sulco, manejo de irrigação, advance, avanço, lcsh:Agriculture (General), furrow, Agricultural and Biological Sciences (miscellaneous), Agronomy and Crop Science, lcsh:S1-972, desempenho, performance
Abstract

RESUMO Um modelo matemático computacional de ondas cinemáticas foi desenvolvido para interagir num processo de otimização não-linear na solução do problema inverso da irrigação por sulco, que consiste na determinação das características de infiltração d'água no solo, a partir dos dados da medição da fase de avanço. O modelo simula a fase de avanço para diferentes combinações entre os parâmetros de Kostiakov-Lewis, buscando minimizar as discrepâncias entre os tempos de avanço simulado e medido, e faz parte de um programa computacional, denominado SIRTOM (Surface Irrigation Real-Time Optimization Model) desenvolvido para solucionar o problema inverso. Baseando-se na solução inversa encontrada, SIRTOM faz prognósticos do desempenho do sistema de irrigação em tempo real, isto é, durante o evento. A habilidade do modelo em solucionar o problema inverso foi testada para diferentes condições de campo. Efetivou-se o ajuste de avanços simulados com outros medidos em eventos de irrigação sob condições de fluxo contínuo e variável. Como inovação desta pesquisa, a estratégia de manejo com fluxo variável tem a finalidade de alterar a trajetória de avanço, quando detectado que a trajetória atual será uma catástrofe para o desempenho do sistema de irrigação. As análises demonstraram que o modelo de simulação desenvolvido nesta pesquisa é viável na solução do problema inverso, uma vez que, para todas as condições de campo estudadas, ele interagiu satisfatoriamente no processo de ajustagem. Constatou-se que a solução do problema inverso da irrigação por sulco é possível, mesmo durante estágios iniciais da fase de avanço, fato este que viabiliza ao programa SIRTOM fazer diagnósticos do desempenho do sistema de irrigação e sugerir, ao irrigante, alternativas para aprimorá-lo em tempo real. ABSTRACT A kinematic-wave model was developed to interact upon a non-linear optimization process for solving the inverse furrow irrigation problem, which consists to determine the soil water infiltration characteristics from the advance phase measurements. The model simulates the advance phase for different combinations between the Kostiakov-Lewis parameters, purposing to minimize the discrepancies between the simulated and measured advance times. This model is part of a computer program, named SIRTOM (Surface Irrigation Real-Time Optimization Model), developed for solving the inverse problem. Based on the fund inverse solution, SIRTOM predicts the irrigation system performance on a real-time basis, that is, during the irrigation event. The model's ability to solve the inverse problem was tested under different field conditions. The simulated advance fittings were performed for advance phases measured in irrigation events under continuous and variable flow conditions. As an innovation of this research, the variable flow management strategy has the purpose to change the advance trajectory, whenever it would be detected that the current trajectory will be a disaster for the irrigation system performance. The analysis showed that the simulation model developed in this research is viable in the solution of the inverse problem, since for all field conditions tested, it interacted satisfactorily upon the fitting process. It was verified that the solution for the furrow irrigation inverse problem is possible even during early stages of the advance phase, which substantially strengthens the SIRTOM program to make diagnosis of the irrigation system performance and to suggest for the irrigators alternatives for improving it in a real-time basis.

Published
1997

323. Mobile unnatural amino acid side chains in the core of staphylococcal nuclease

Author

Wynn, R., Harkins, P. C., Richards, F. M., and Fox, R. O.

Subjects
Bacterial Proteins, Protein Conformation, Mutation, Micrococcal Nuclease, Cysteine, Sulfhydryl Compounds, Amino Acids, Crystallography, X-Ray, Research Article
Abstract

The structures of several variants of staphylococcal nuclease with long flexible unnatural amino acid side chains in the hydrophobic core have been determined by X-ray crystallography. The unnatural amino acids are disulfide moieties between the lone cysteine residue in V23C nuclease and methane, ethane, 1-n-propane, 1-n-butane, 1-n-pentane, and 2-hydroxyethyl thiols. We have examined changes in the core packing of these mutants. Side chains as large as the 1-n-propyl cysteine disulfide can be incorporated without perturbation of the structure. This is due, in part, to cavities present in the wild-type protein. The longest side chains are not well defined, even though they remain buried within the protein interior. These results suggest that the enthalpy-entropy balance that governs the rigidity of protein interiors favors tight packing only weakly. Additionally, the tight packing observed normally in protein interiors may reflect, in part, the limited numbers of rotamers available to the natural amino acids.

Published
1996

324. Survey on haematopoietic stem cell transplantation for children in Europe

Author

Miano, M, Cancedda, Ranieri, Hartmann, O, Cornish, J, Locatelli, Franco, Egeler, R M, Slavin, S, Veys, P, Ortega, J, Peters, C, Wynn, R F, Iori, A P, Fagioli, F, Ljungmann, P, Niethammer, D, Bordigoni, P, Dini, G, Cancedda, R, Locatelli, F (ORCID:0000-0002-7976-3654), Miano, M, Cancedda, Ranieri, Hartmann, O, Cornish, J, Locatelli, Franco, Egeler, R M, Slavin, S, Veys, P, Ortega, J, Peters, C, Wynn, R F, Iori, A P, Fagioli, F, Ljungmann, P, Niethammer, D, Bordigoni, P, Dini, G, Cancedda, R, and Locatelli, F (ORCID:0000-0002-7976-3654)

Abstract

A recent report, prepared in March 2003, regarding the paediatric transplantation activity registered between 1970 and 2002 in the European Bone Marrow Transplantation (EBMT) database showed a decrease in the number of registrations in 2001 and in 2002. In order to validate this observation, the Paediatric Diseases Working Party (PDsWP) secretariat distributed a questionnaire to 395 institutions participating in the EBMT Registry. Each institution was requested to check the number of transplants they reported and to confirm or to correct the figures. As of 15 March 2004, replies had been received from 135 centres reporting a median of 48 transplants per centre over the study period, total 17 891 (58% of the total number). Among them, 55 confirmed their original figures, while 80 corrected the numbers. The overall number of autologous and allogeneic SCTs performed and not reported were 461 and 692, respectively. Most of the teams that corrected their figures stated that their data managers could provide missing data to the EBMT; 260 other teams, each reporting a median of 15 transplants during the study period, total 12 866 (42% of the total number) chose not to reply. A report prepared in March 2004, following the PDsWP survey, showed an increasing number of transplants performed on patients below 18 years of age between 1973 and 2002 and reported to the EBMT Registry ( 328 autologous and 628 allogeneic) as compared to the 2003 report. This first PDsWP survey, reaching more than 50% of activity in the field, illustrates that the decrease in activity we observed in the 2003 report does not correspond to a decrease in the number of transplants that were actually performed. It demonstrates the compliance of most major paediatric institutions and confirms the important role of cooperation between National Registries and EBMT Registries.

Published
2005

332. Allogeneic stem cell transplantation for refractory acute myeloid leukemia in pediatric patients: the UK experience

Author

O'Hare, P, Lucchini, G, Cummins, M, Veys, P, Potter, M, Lawson, S, Vora, A, Wynn, R, Peniket, A, Kirkland, K, Pearce, R, Perry, J, and Amrolia, P J

Abstract

We report outcomes for 44 children who underwent stem cell transplantation (SCT) for refractory AML in the UK between 2000 and 2012. Median age at SCT was 11.5 years. Twenty-three patients had primary refractory and 21 relapsed refractory AML. Refractory disease was confirmed by cytogenetics/molecular genetics in 24 cases. Median follow-up of the whole cohort is 6.8 years (2.1–14.9 years). Thirty patients (68%) achieved a CR following SCT. Transplant-related mortality at 1 year was 18%. Acute GVHD incidence was 52% (grade ⩾III 19%), chronic 7%. Relapse was the major cause of treatment failure and occurred in 32% of patients at a median of 61 days post SCT. Five-year overall survival and leukemia-free survival (LFS) were 43% (95% CI 31–61%). All patients with favorable cytogenetics (n=6) are alive in CR. Outcomes in patients with primary refractory disease were equivalent to those with relapsed refractory AML. Blast percentage ⩽30% in the BM pre-SCT, myeloablative conditioning and acute GVHD proved to be favorable prognostic features. We could stratify patients according to age ⩾10 years and >30% blasts in BM pre-SCT. Patients with none/one of these risk factors were highly salvageable (5 years LFS 53%) whereas those with both factors had a very poor prognosis (5 years LFS 10%). This may facilitate decision making on whether it is appropriate to consider transplant in such patients.

Published
2017
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333. Changes in the incidence, patterns and outcomes of graft failure following hematopoietic stem cell transplantation for Hurler syndrome

Author

Lum, S H, Miller, W P, Jones, S, Poulton, K, Ogden, W, Lee, H, Logan, A, Bonney, D, Lund, T C, Orchard, P J, and Wynn, R F

Abstract

Hematopoietic stem cell transplantation (HSCT) is the standard of care in children with Hurler syndrome (HS) as it is the only therapy that can arrest disease progression. We examined the incidence, patterns and outcomes of graft failure in all HS children undergoing first HSCT at the Royal Manchester Children’s Hospital or the University of Minnesota Children’s Hospital from 1983 to 2016. Implementation of busulfan pharmacokinetic monitoring started in 2004 in both institutions. Two hundred and forty HS children were included in this analysis (historical era (pre-2004), n=131; current era (post 2004), n=109). The proportion of patients with graft failure was significantly lower in the current era compared with the historical era (37.2% vs 10.1%, respectively). Of 49 patients with graft failure in the historical era, 1 had aplasia and 48 had autologous reconstitution. All the 11 graft failures of the current era occurred in recipients of cord blood transplants (7 aplasia and 4 autologous reconstitution). The outcomes of second transplant in these patients has improved, with 89% of such patients alive and engrafted in the current era compared with 58% in the historical era. The pattern of graft failure has changed from autologous reconstitution, likely secondary to inadequate myelosuppression in the historical era, to aplasia in the current era, likely due to imperfect immunosuppression.

Published
2017
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339. Chronic norovirus infection in pediatric hematopoietic stem cell transplant recipients: A cause of prolonged intestinal failure requiring intensive nutritional support

Author

Saif, M. A., primary, Bonney, D. K., additional, Bigger, B., additional, Forsythe, L., additional, Williams, N., additional, Page, J., additional, Babiker, Z. O., additional, Guiver, M., additional, Turner, A. J., additional, Hughes, S., additional, and Wynn, R. F., additional

Published
2011
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342. Alemtuzumab-Based Conditioning Protocols for Paediatric Matched Unrelated Donor Transplants for Severe Aplastic Anaemia: An Important Alternative to TBI Containing Regimens

Author

Samarasinghe, S., primary, Steward, C., additional, Hiwarkar, P., additional, Bonney, D., additional, Keogh, S., additional, Rao, K., additional, Amrolia, P., additional, Goulden, N., additional, Mathew, S., additional, Hough, R., additional, Wynn, R., additional, and Veys, P., additional

Published
2011
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346. Contributors

Author

Mew, Nicholas Ah, Akamatsu, Wado, Akman, Hasan Orhan, Aoyama, Koji, Arnold, W. David, Artuch, Rafael, Bachoo, Robert M., Baranzini, Sergio E., Beck, Michael, Benson, Merrill D., Berginer, Vladimir M., Berry, Gerard T., Biglan, Kevin M., Bird, Thomas D., Montgomery Bissell, D., Bloch, Michael H., Broccolini, Aldobrando, Brown, Robert H., Jr., Caban-Holt, Allison, Canine, Brenda, Caskey, C. Thomas, Chinnery, Patrick F., Chuang, David T., Chuang, Jacinta L., Cohen, Bernard A., Comi, Anne M., Cox, Rody P., Crabbe, John C., Davis, Marie Y., De Vivo, Darryl C., Desnick, Robert J., Di Donato, Stefano, DiMauro, Salvatore, Dowling, Michael M., Dyment, David A., Eichler, Florian S., Elangovan, Ramyiadarsini, Elger, Bernice, Elrefai, Sara, Elroy-Stein, Orna, Elsheikh, Bakri H., Engel, Andrew G., Evans, Patricia, Fahn, Stanley, Fears, Scott C., Fink, John K., Friedmann, Theodore, Gallagher, Martin J., García-Cazorla, Àngels, Goldman, Jill S., Golla, Sailaja, Gospe, Sidney M., Jr., Graf, William D., Griggs, Robert C., Gropman, Andrea L., Gu, Yian, Gunn, Teresa M., Gutmann, David H., Haas, Richard, Hagerman, Randi J., Haltia, Matti J., Hare, Emma B., Harel, Tamar, Hauser, Stephen L., Head, Elizabeth, Hilbert, James E., Hoffman, Eric P., Iliopoulos, Othon, Ishiura, Hiroyuki, Islam, Monica P., Jack, Clifford R., Jr., Johnson, William G., Jotterand, Fabrice, Jungbluth, Heinz, Kane, John P., van Karnebeek, Clara, Kayani, Saima N., Khemani, Pravin, Kirkham, Fenella J., Kirkorian, A. Yasmine, Kissel, John T., Klein, Christine, Kleopa, Kleopas A., Kono, Satoshi, Kruer, Michael C., Kukull, Walter A., Lennington, Jessica B., Lewis, David A., Liang, Wen-Chen, Lohmann, Katja, Lombroso, Paul J., Lozano, Reymundo, Lupski, James R., Luzi, Paola, Ma, Qian, Macdonald, Robert L., Maegawa, Gustavo H.B., Maher, Elizabeth A., Malloy, Mary J., Mankodi, Ami K., Marchek, Douglas A., Marin-Valencia, Isaac, Marshall, Frederick J., Mastrianni, James A., Matalon, Reuben, Mayeux, Richard, McCurdy, Jennifer L., McGarry, Andrew J., Menkes, John H., Meola, Giovanni, Metelo, Ana, Matalon, Kimberlee Michals, Miller, Bruce L., Mirabella, Massimiliano, Miron, Justin, Mitsui, Jun, Miyajima, Hiroaki, Mizutani, Shuki, Mole, Sara E., Monteggia, Lisa M., Moser, Hugo W., Morris, Mary Ann, Moxley, Richard T., III, Mueller, Jennifer M., Muntoni, Francesco, Murray, Melissa E., Nakaki, Toshio, Nemeroff, Charles B., Nishino, Ichizo, Nyhan, William L., Okano, Hideyuki, Oksenberg, Jorge R., Ostendorf, Adam P., Pandolfo, Massimo, Pappa, Maria Belen, Paradas, Carmen, Pascual, Juan M., Pastores, Gregory M., Patel, Shailendra B., Patterson, Marc C., Pehlivan, Davut, Philibin, Scott D., Picard, Cynthia, Poirier, Judes, Ptáček, Louis J., Radhakrishnan, Geetha L., Ralph, Jeffrey W., Ramagopalan, Sreeram V., Raymond, Gerald V., Renthal, William, Reus, Victor I., Roach, E. Steve, Rosenberg, Roger N., Rosenblatt, David S., Salen, Gerald, Sandhoff, Konrad, Scahill, Lawrence D., Scherer, Steven S., Schiffmann, Raphael, Schindler, Detlev, Schmitt, Frederick, Schneider, Susanne A., Schon, Eric A., Schuchman, Edward H., Schupf, Nicole, Seashore, Margretta Reed, Selkoe, Dennis J., Sewry, Caroline, Shevell, Michael, Shinagawa, Shunichiro, Sreedharan, Jemeen, Srour, Myriam, Sugie, Kazuma, Szabla, Kristen L., Szabo, Steven T., Szuhay, Gábor, Taroni, Franco, Tawil, Rabi, Tondo, Mireia, Tsuji, Shoji, Udd, Bjarne, Uhlmann, Wendy R., Vaccarino, Flora M., Vemuri, Prashanthi, Venditti, Charles P., Volk, David W., Wang, Dong, Watkins, David, Wenger, David A., Williams, Charles A., Wilson, Kathleen S., Wilson, Golder N., Wolf, Barry, Max Wynn, R., and Yu, Shihui

Published
2015
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348. Phenylbutyrate therapy for maple syrup urine disease

Author

Brunetti-Pierri, Nicola, primary, Lanpher, Brendan, additional, Erez, Ayelet, additional, Ananieva, Elitsa A., additional, Islam, Mohammad, additional, Marini, Juan C., additional, Sun, Qin, additional, Yu, Chunli, additional, Hegde, Madhuri, additional, Li, Jun, additional, Wynn, R. Max, additional, Chuang, David T., additional, Hutson, Susan, additional, and Lee, Brendan, additional

Published
2010
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