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1. Effects of abiotic stress on gene transcription in European beech: ozone affects ethylene biosynthesis in saplings of Fagus sylvatica L.

Author

Betz GA, Gerstner E, Olbrich M, Winkler JB, Langebartels C, Heller W, Sandermann H, and Ernst D

Subjects
Abiotic stress, Ethylene biosynthesis, Fagus sylvatica, Gene expression, Ozone, Forestry, SD1-669.5
Abstract

The influence of ozone (150-190 nl L-1; 8h/d) on transcription levels of genes involved in the biosynthesis of the stress hormone ethylene, and its precursor 1-aminocyclopropane-1-carboxylate (ACC), was analysed in leaves of European beech saplings. Ozone-induced leaf lesions appeared 7 weeks after onset of ozone exposure. Cell lesion formation was preceded by persistent increases in ethylene emission, in the level of its malonylated precursor ACC, and in the transcript levels of specific ACC synthase 1 (ACS1), ACS2, ACC oxidase 1 (ACO1), and ACO2. Our results demonstrate that mechanisms similar to those operating in herbaceous plants may determine beech saplings responses to ozone exposure.

Published
2009
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2. Testing a New Monte Carlo Strategy for Folding Model Proteins

Author

Frauenkron, H., Bastolla, U., Gerstner, E., Grassberger, P., and Nadler, und W.

Subjects
Condensed Matter - Soft Condensed Matter, Quantitative Biology
Abstract

We demonstrate that the recently proposed pruned-enriched Rosenbluth method PERM (P.~Grassberger, Phys.~Rev.~{\bf E 56} (1997) 3682) leads to very efficient algorithms for the folding of simple model proteins. We test it on several models for lattice heteropolymers, and compare to published Monte Carlo studies of the properties of particular sequences. In all cases our method is faster than the previous ones, and in several cases we find new minimal energy states. In addition to producing more reliable candidates for ground states, our method gives detailed information about the thermal spectrum and, thus, allows to analyze static aspects of the folding behavior of arbitrary sequences., Comment: 17 pages, 21 figures, needs mprocl.sty (included), appears in Workshop on: Monte Carlo Approach to Biopolymers and Protein Folding, World Scientific 1998

Published
1998

3. P06.11.B NEUROTOXICITY AND MANAGEMENT OF PRIMARY AND SECONDARY CNS LYMPHOMA AFTER ADOPTIVE IMMUNOTHERAPY WITH CD19-DIRECTED CAR T-CELLS

Author

Karschnia, P, primary, Arrillaga-Romany, I C, additional, Eichler, A, additional, Forst, D A, additional, Gerstner, E, additional, Jordan, J T, additional, Ly, I, additional, Plotkin, S R, additional, Wang, N, additional, Martinez-Lage, M, additional, Winter, S F, additional, Tonn, J, additional, Rejeski, K, additional, von Baumgarten, L, additional, Cahill, D P, additional, Nahed, B V, additional, Shankar, G M, additional, Abramson, J S, additional, Barnes, J A, additional, El-Jawahri, A, additional, Hochberg, E P, additional, Johnson, P, additional, Soumerai, J D, additional, Takvorian, R W, additional, Chen, Y, additional, Frigault, M J, additional, and Dietrich, J, additional

Published
2023
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4. Cryogen spray cooling of human skin: Effects of ambient humidity level, spraying distance, and cryogen boiling point

Author

Anvari, B, Ver Steeg, BJ, Milner, TE, Tanenbaum, BS, Klein, TJ, Gerstner, E, Kimel, S, and Nelson, JS

Subjects
alternative refrigerants, cutaneous hypervascular lesions, dermatology, lasers, port wine stains, rhytides, selective thermal injury
Abstract

Recent studies have shown spray cooling of the skin surface with millisecond cryogen spurts to be an effective method for protecting the epidermis from non-specific thermal injury during various laser mediated dermatological procedures. We have investigated the effects of ambient humidity level, spraying distance, and cryogen boiling point on the resulting radiometric surface temperature. Our findings indicate that: 1) decreasing the ambient humidity level results in less ice formation on the skin surface without altering the radiometric surface temperature during a cryogen spurt; 2) increasing the spraying distance to 85 mm lowers the radiometric surface temperature; and 3) boiling point of the cryogen does not directly affect the surface temperature in the geometries studied.

Published
1997

5. Managing service shutdowns: Cash refunds or vouchers?

Author

Chen R. R., Gerstner E., Halbheer D., Roma P., Chen R.R., Gerstner E., Halbheer D., and Roma P.

Subjects
Cash refund, Marketing, Service failure and recovery, Service shutdown, Voucher, Service replacement
Abstract

Service shutdowns—extended disruptions of operations—caused by exogenous events are on the rise. Such shutdowns pose major challenges for service providers, customers, and regulators. Providers prefer vouchers as a means of service recovery to limit bankruptcy risk, whereas customers demand cash refunds or vouchers that include a generous bonus. Regulators, on the other hand, insist that customers must be granted the right to be reimbursed in cash. This paper shows that a zero bonus is optimal under the voucher-only strategy, whereas the provider should always include a positive bonus with the voucher under the hybrid strategy that allows customers to choose between the cash refund and voucher options. Surprisingly, despite its higher flexibility in service recovery design, the hybrid strategy can be dominated by the voucher-only strategy in terms of profit and welfare. Moreover, we show that the ranking of strategies differs across the two important dimensions of expected profit and survival under shutdown. Finally, we study competition among providers and show that a high-quality provider is more likely to use cash-back as the service recovery strategy than its low-quality competitor.

Published
2022
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9. Response to Letter to Editor

Author

Kaufmann, TJ, Smits, Marion, Boxerman, J, Huang, R, Barboriak, DP, Weller, M, Chung, C, Tsien, C, Brown, PD, Shankar, L, Galanis, E, Gerstner, E, van den Bent, Martin, Burns, TC, Parney, IF, Dunn, G, Brastianos, PK, Lin, NU, Wen, PY, Ellingson, BM, Kaufmann, TJ, Smits, Marion, Boxerman, J, Huang, R, Barboriak, DP, Weller, M, Chung, C, Tsien, C, Brown, PD, Shankar, L, Galanis, E, Gerstner, E, van den Bent, Martin, Burns, TC, Parney, IF, Dunn, G, Brastianos, PK, Lin, NU, Wen, PY, and Ellingson, BM

Published
2020

13. Growth of CrSi[sub 2] by radiation enhanced diffusion at room temperature.

Author

Shannon, J. M., Hoyland, J. D., and Gerstner, E. G.

Subjects
CHROMIUM compounds, ION bombardment, SILICON
Abstract

Chromium disilicide layers have been formed by ion bombardment through a chromium layer into silicon at room temperature. It was found that the thickness of the silicide formed under the chromium layer was similar for hydrogenated amorphous silicon, laser crystallized silicon, and crystalline silicon substrates. The growth was consistent with a radiation enhanced diffusion mechanism in which the rate limiting process was the diffusion of silicon or chromium through the silicide. It was found that the amount of chromium in the silicide and its thickness were proportional to the square root of the total amount of energy dissipated by the ion beam at the interface between the chromium and the substrate. [ABSTRACT FROM AUTHOR]

Published
2002
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14. Treatment Response Assessment in IDH-Mutant Glioma Patients by Noninvasive 3D Functional Spectroscopic Mapping of 2-Hydroxyglutarate

Author

Koch Institute for Integrative Cancer Research at MIT, Vander Heiden, Matthew G., Andronesi, O. C., Loebel, F., Bogner, W., Marjanska, M., Iafrate, A. J., Dietrich, J., Batchelor, T. T., Gerstner, E. R., Kaelin, W. G., Chi, A. S., Rosen, B. R., Cahill, D. P., Koch Institute for Integrative Cancer Research at MIT, Vander Heiden, Matthew G., Andronesi, O. C., Loebel, F., Bogner, W., Marjanska, M., Iafrate, A. J., Dietrich, J., Batchelor, T. T., Gerstner, E. R., Kaelin, W. G., Chi, A. S., Rosen, B. R., and Cahill, D. P.

Abstract

Purpose: Measurements of objective response rates are critical to evaluate new glioma therapies. The hallmark metabolic alteration in gliomas with mutant isocitrate dehydrogenase (IDH) is the overproduction of oncometabolite 2-hydroxyglutarate (2HG), which plays a key role in malignant transformation. 2HG represents an ideal biomarker to probe treatment response in IDH-mutant glioma patients, and we hypothesized a decrease in 2HG levels would be measureable by in vivo magnetic resonance spectroscopy (MRS) as a result of antitumor therapy. Experimental Design: We report a prospective longitudinal imaging study performed in 25 IDH-mutant glioma patients receiving adjuvant radiation and chemotherapy. A newly developed 3D MRS imaging was used to noninvasively image 2HG. Paired Student t test was used to compare pre- and posttreatment tumor 2HG values. Test-retest measurements were performed to determine the threshold for 2HG functional spectroscopic maps (fSM). Univariate and multivariate regression were performed to correlate 2HG changes with Karnofsky performance score (KPS). Results: We found that mean 2HG (2HG/Cre) levels decreased significantly (median=48.1%; 95% confidence interval=27.3%-56.5%; P=0.007) in the posttreatment scan. The volume of decreased 2HG correlates (R2=0.88, P=0.002) with clinical status evaluated by KPS. Conclusions: We demonstrate that dynamic measurements of 2HG are feasible by 3D fSM, and the decrease of 2HG levels can monitor treatment response in patients with IDH-mutant gliomas. Our results indicate that quantitative in vivo 2HG imaging maybe used for precision medicine and early response assessment in clinical trials of therapies targeting IDH-mutant gliomas.

Published
2018

15. Consensus recommendations for a standardized Brain Tumor Imaging Protocol in clinical trials

Author

Ellingson, BM, Bendszus, M, Boxerman, J, Barboriak, D, Erickson, BJ, Smits, M, Nelson, SJ, Gerstner, E, Alexander, B, Goldmacher, G, Wick, W, Vogelbaum, M, Weller, M, Galanis, E, Kalpathy-Cramer, J, Shankar, L, Jacobs, P, Pope, WB, Yang, D, Chung, C, Knopp, MV, Cha, S, Van Den Bent, MJ, Chang, S, Al Yung, WK, Cloughesy, TF, Wen, PY, Gilbert, MR, Whitney, A, Sandak, D, Musella, A, Haynes, C, Wallace, M, Arons, DF, and Kingston, A

Abstract

© 2015 The Author(s). A recent joint meeting was held on January 30, 2014, with the US Food and Drug Administration (FDA), National Cancer Institute (NCI), clinical scientists, imaging experts, pharmaceutical and biotech companies, clinical trials cooperative groups, and patient advocate groups to discuss imaging endpoints for clinical trials in glioblastoma. This workshop developed a set of priorities and action items including the creation of a standardized MRI protocol for multicenter studies. The current document outlines consensus recommendations for a standardized Brain Tumor Imaging Protocol (BTIP), along with the scientific and practical justifications for these recommendations, resulting from a series of discussions between various experts involved in aspects of neuro-oncology neuroimaging for clinical trials. The minimum recommended sequences include: (i) parameter-matched precontrast and postcontrast inversion recovery-prepared, isotropic 3D T1-weighted gradient-recalled echo; (ii) axial 2D T2-weighted turbo spin-echo acquired after contrast injection and before postcontrast 3D T1-weighted images to control timing of images after contrast administration; (iii) precontrast, axial 2D T2-weighted fluid-attenuated inversion recovery; and (iv) precontrast, axial 2D, 3-directional diffusion-weighted images. Recommended ranges of sequence parameters are provided for both 1.5 T and 3 T MR systems.

Published
2015
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16. Structural investigation of two carbon nitride solids produced by cathodic arc deposition and nitrogen implantation.

Author

Merchant, A. R., McCulloch, D. G., McKenzie, D. R., Yin, Y., Hall, L., and Gerstner, E. G.

Subjects
NITRIDES, SOLID state electronics, CATHODES
Abstract

Presents information on a study that found that the structures of the carbon nitride materials produced by cathodic arc deposition and nitrogen implantation of glassy carbon were similar. Experimental procedure; Results and discussion on the study; Conclusions.

Published
1996
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18. Consensus recommendations for a standardized Brain Tumor Imaging Protocol in clinical trials

Author

Ellingson, B.M. (Benjamin M.), Bendszus, M. (Martin), Boxerman, J. (Jerrold), Barboriak, D. (Daniel), Erickson, B.J. (Bradley J.), Smits, M. (Marion), Nelson, S.J. (Sarah J.), Gerstner, E. (Elizabeth), Alexander, B. (Brian), Goldmacher, G. (Gregory), Wick, W. (Wolfgang), Vogelbaum, M.A. (Michael), Weller, M. (Michael), Galanis, E. (Evanthia), Kalpathy-Cramer, J. (Jayashree), Shankar, L., Jacobs, P. (Paula), Pope, W.B. (Whitney B.), Yang, D. (Dewen), Chung, C. (Caroline), Knopp, R.H., Cha, S. (Soonme), Bent, M.J. (Martin) van den, Chang, S.M. (Susan), Al Yung, W.K., Cloughesy, T.F. (Timothy F.), Wen, P.Y. (Patrick Y.), Gilbert, M.R. (Mark R.), Whitney, A. (Andrew), Sandak, D. (David), Musella, A. (Al), Haynes, C. (Chas), Wallace, M. (Max), Arons, D.F. (David F.), Kingston, A. (Ann), Ellingson, B.M. (Benjamin M.), Bendszus, M. (Martin), Boxerman, J. (Jerrold), Barboriak, D. (Daniel), Erickson, B.J. (Bradley J.), Smits, M. (Marion), Nelson, S.J. (Sarah J.), Gerstner, E. (Elizabeth), Alexander, B. (Brian), Goldmacher, G. (Gregory), Wick, W. (Wolfgang), Vogelbaum, M.A. (Michael), Weller, M. (Michael), Galanis, E. (Evanthia), Kalpathy-Cramer, J. (Jayashree), Shankar, L., Jacobs, P. (Paula), Pope, W.B. (Whitney B.), Yang, D. (Dewen), Chung, C. (Caroline), Knopp, R.H., Cha, S. (Soonme), Bent, M.J. (Martin) van den, Chang, S.M. (Susan), Al Yung, W.K., Cloughesy, T.F. (Timothy F.), Wen, P.Y. (Patrick Y.), Gilbert, M.R. (Mark R.), Whitney, A. (Andrew), Sandak, D. (David), Musella, A. (Al), Haynes, C. (Chas), Wallace, M. (Max), Arons, D.F. (David F.), and Kingston, A. (Ann)

Abstract

A recent joint meeting was held on January 30, 2014, with the US Food and Drug Administration (FDA), National Cancer Institute (NCI), clinical scientists, imaging experts, pharmaceutical and biotech companies, clinical trials cooperative groups, and patient advocate groups to discuss imaging endpoints for clinical trials in glioblastoma. This workshop developed a set of priorities and action items including the creation of a standardized MRI protocol for multicenter studies. The current document outlines consensus recommendations for a standardized Brain Tumor Imaging Protocol (BTIP), along with the s

Published
2015
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19. Consensus recommendations for a standardized Brain Tumor Imaging Protocol in clinical trials

Author

Ellingson, B M, Bendszus, M, Boxerman, J, Barboriak, D, Erickson, B J, Smits, M, Nelson, S J, Gerstner, E, Alexander, B, Goldmacher, G, Wick, W, Vogelbaum, M, Weller, M, Galanis, E, Kalpathy-Cramer, J, Shankar, L, Jacobs, P, Pope, W B, Yang, D, Chung, C, Knopp, M V, Cha, S, van den Bent, M J, Chang, S, Al Yung, W K, Cloughesy, T F, Wen, P Y, Gilbert, M R, Ellingson, B M, Bendszus, M, Boxerman, J, Barboriak, D, Erickson, B J, Smits, M, Nelson, S J, Gerstner, E, Alexander, B, Goldmacher, G, Wick, W, Vogelbaum, M, Weller, M, Galanis, E, Kalpathy-Cramer, J, Shankar, L, Jacobs, P, Pope, W B, Yang, D, Chung, C, Knopp, M V, Cha, S, van den Bent, M J, Chang, S, Al Yung, W K, Cloughesy, T F, Wen, P Y, and Gilbert, M R

Abstract

A recent joint meeting was held on January 30, 2014, with the US Food and Drug Administration (FDA), National Cancer Institute (NCI), clinical scientists, imaging experts, pharmaceutical and biotech companies, clinical trials cooperative groups, and patient advocate groups to discuss imaging endpoints for clinical trials in glioblastoma. This workshop developed a set of priorities and action items including the creation of a standardized MRI protocol for multicenter studies. The current document outlines consensus recommendations for a standardized Brain Tumor Imaging Protocol (BTIP), along with the scientific and practical justifications for these recommendations, resulting from a series of discussions between various experts involved in aspects of neuro-oncology neuroimaging for clinical trials. The minimum recommended sequences include: (i) parameter-matched precontrast and postcontrast inversion recovery-prepared, isotropic 3D T1-weighted gradient-recalled echo; (ii) axial 2D T2-weighted turbo spin-echo acquired after contrast injection and before postcontrast 3D T1-weighted images to control timing of images after contrast administration; (iii) precontrast, axial 2D T2-weighted fluid-attenuated inversion recovery; and (iv) precontrast, axial 2D, 3-directional diffusion-weighted images. Recommended ranges of sequence parameters are provided for both 1.5 T and 3 T MR systems.

Published
2015

26. INCREASED PERFUSION DUE TO VASCULAR NORMALIZATION IMPROVES OXYGENATION AND SURVIVAL IN GLIOBLASTOMA PATIENTS TREATED WITH CEDIRANIB WITH OR WITHOUT CHEMORADIATION

Author

Batchelor, T. T., primary, Gerstner, E. R., additional, Emblem, K. E., additional, Duda, D. G., additional, Kalpathy-Cramer, J., additional, Snuderl, M., additional, Ancukiewicz, M., additional, Polaskova, P., additional, Pinho, M. C., additional, Jennings, D., additional, Plotkin, S. R., additional, Chi, A. S., additional, Eichler, A. F., additional, Dietrich, J., additional, Hochberg, F. H., additional, Lu-Emerson, C., additional, Iafrate, A. J., additional, Ivy, S. P., additional, Rosen, B., additional, Loeffler, J. S., additional, Wen, P. Y., additional, Sorensen, A. G., additional, and Jain, R. K., additional

Published
2014
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28. Regionaler Klimaatlas Deutschland der Helmholtz-Gemeinschaft informiert im Internet über möglichen künftigen Klimawandel

Author

Meinke, I., Gerstner, E., von Storch, H., Marx, Andreas, Schipper, H., Kottmeier, C., Treffeisen, R., Lemke, P., Meinke, I., Gerstner, E., von Storch, H., Marx, Andreas, Schipper, H., Kottmeier, C., Treffeisen, R., and Lemke, P.

Abstract

Wie unterschiedlich sich der Klimawandel in den einzelnen Bundesländern künftig auswirken kann, zeigt seit Februar 2010 der Regionale Klimaatlas Deutschland. Unter www.regionaler-klimaatlas.de sind mögliche Klimaszenarien für die deutschen Bundesländer im Internet abrufbar. Nach Vorbild des Norddeutschen Klimaatlas verfolgt der Regionale Klimaatlas Deutschland einen Ensembleansatz: Aus derzeit 12 regionalen Klimaprojektionen werden Spannbreiten für mögliche künftige Klimaänderungen bestimmt. Nutzer können dabei verschiedene Klimaelemente und daraus abgeleitete Größen auswählen und sich über mögliche künftige Änderungen zu unterschiedlichen Jahreszeiten in verschiedenen Bundesländern informieren. Der zu betrachtende Zeithorizont kann flexibel für individuelle Planungszwecke ausgewählt werden. Der Klimaatlas richtet sich an die interessierte Öffentlichkeit sowie an Entscheidungsträger aus Politik und Wirtschaft. Alternativ steht zusätzlich eine Darstellung für Modellnutzer zur Verfügung.

Published
2010

29. Increase in tumor-associated macrophages after antiangiogenic therapy is associated with poor survival among patients with recurrent glioblastoma

Author

Lu-Emerson, C., primary, Snuderl, M., additional, Kirkpatrick, N. D., additional, Goveia, J., additional, Davidson, C., additional, Huang, Y., additional, Riedemann, L., additional, Taylor, J., additional, Ivy, P., additional, Duda, D. G., additional, Ancukiewicz, M., additional, Plotkin, S. R., additional, Chi, A. S., additional, Gerstner, E. R., additional, Eichler, A. F., additional, Dietrich, J., additional, Stemmer-Rachamimov, A. O., additional, Batchelor, T. T., additional, and Jain, R. K., additional

Published
2013
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31. ANGIOGENESIS AND INVASION

Author

Hu, Y.-L., primary, De Lay, M., additional, Rose, S. D., additional, Carbonell, W. S., additional, Aghi, M. K., additional, Hu, Y.-L., additional, Paquette, J., additional, Tokuyasu, T., additional, Tsao, S., additional, Chaumeil, M., additional, Ronen, S., additional, Matlaf, L. A., additional, Soroceanu, L., additional, Cobbs, C., additional, Matlaf, L., additional, Harkins, L., additional, Garzon-Muvdi, T., additional, Rhys, C. a., additional, Smith, C., additional, Kim, D.-H., additional, Kone, L., additional, Farber, H., additional, An, S., additional, Levchenko, A., additional, Quinones-Hinojosa, A., additional, Lemke, D., additional, Pfenning, P.-N., additional, Sahm, F., additional, Klein, A.-C., additional, Kempf, T., additional, Schnolzer, M., additional, Platten, M., additional, Wick, W., additional, Smith, S. J., additional, Rahman, R., additional, Rahman, C., additional, Barrow, J., additional, Macarthur, D., additional, Rose, F., additional, Grundy, R. G., additional, Kaley, T. J., additional, Huse, J., additional, Karimi, S., additional, Rosenblum, M., additional, Omuro, A., additional, DeAngelis, L. M., additional, de Groot, J. F., additional, Kong, L.-Y., additional, Wei, J., additional, Wang, T., additional, Piao, Y., additional, Liang, J., additional, Fuller, G. N., additional, Qiao, W., additional, Heimberger, A. B., additional, Jhaveri, N., additional, Cho, H., additional, Torres, S., additional, Wang, W., additional, Schonthal, A., additional, Petasis, N., additional, Louie, S. G., additional, Hofman, F., additional, Chen, T. C., additional, Yamada, R., additional, Sumual, S., additional, Buljan, V., additional, Bennett, M. R., additional, McDonald, K. L., additional, Weiler, M., additional, Thiepold, A.-L., additional, Jestaedt, L., additional, Gronych, J., additional, Dittmann, L. M., additional, Jugold, M., additional, Kosch, M., additional, Combs, S. E., additional, von Deimling, A., additional, Weller, M., additional, Bendszus, M., additional, Kwiatkowska, A., additional, Paulino, V., additional, Tran, N. L., additional, Symons, M., additional, Stockham, A. L., additional, Borden, E., additional, Peereboom, D., additional, Hu, Y., additional, Chaturbedi, A., additional, Hamamura, M., additional, Mark, E., additional, Zhou, Y.-H., additional, Abbadi, S., additional, Guerrero-Cazares, H., additional, Pistollato, F., additional, Smith, C. L., additional, Ruff, W., additional, Puppa, A. D., additional, Basso, G., additional, Monje, M., additional, Freret, M. E., additional, Masek, M., additional, Fisher, P. G., additional, Haddix, T., additional, Vogel, H., additional, Kijima, N., additional, Hosen, N., additional, Kagawa, N., additional, Hashimoto, N., additional, Fujimoto, Y., additional, Kinoshita, M., additional, Sugiyama, H., additional, Yoshimine, T., additional, Anneke, N., additional, Bob, H., additional, Pieter, W., additional, Arend, H., additional, William, L., additional, Eoli, M., additional, Calleri, A., additional, Cuppini, L., additional, Anghileri, E., additional, Pellegatta, S., additional, Prodi, E., additional, Bruzzone, M. G., additional, Bertolini, F., additional, Finocchiaro, G., additional, Zhu, D., additional, Hunter, S. B., additional, Vertino, P. M., additional, Van Meir, E. G., additional, Cork, S. M., additional, Kaur, B., additional, Cooper, L., additional, Saltz, J. H., additional, Sandberg, E. M., additional, Burrell, K., additional, Hill, R., additional, Zadeh, G., additional, Parker, J. J., additional, Dionne, K., additional, Massarwa, R., additional, Klaassen, M., additional, Niswander, L., additional, Kleinschmidt-DeMasters, B. K., additional, Waziri, A., additional, Jalali, S., additional, Wataya, T., additional, Salehi, F., additional, Croul, S., additional, Gentili, F., additional, Foltz, W., additional, Lee, J.-I., additional, Agnihorti, S., additional, Menard, C., additional, Chung, C., additional, Schonthal, A. H., additional, Hofman, F. M., additional, Elena, P., additional, Faivre, G., additional, Demopoulos, A., additional, Taillibert, S., additional, Kirsch, M., additional, Martin, K. D., additional, Bertram, A., additional, uckermann, O., additional, Leipnitz, E., additional, Weigel, P., additional, Temme, A., additional, Schackert, G., additional, Geiger, K., additional, Gerstner, E., additional, Jennings, D., additional, Chi, A. S., additional, Plotkin, S., additional, Kwon, S. J., additional, Pinho, M., additional, Polaskova, P., additional, Batchelor, T. T., additional, Sorensen, A. G., additional, Hossain, M. B., additional, Gururaj, A. E., additional, Cortes-Santiago, N., additional, Gabrusiewicz, K., additional, Yung, W. K. A., additional, Fueyo, J., additional, Gomez-Manzano, C., additional, Gil, O. D., additional, Noticewala, S., additional, Ivkovic, S., additional, Esencay, M., additional, Zagzagg, D., additional, Rosenfeld, S., additional, Bruce, J. N., additional, Canoll, P., additional, Chang, J. H., additional, Seol, H. J., additional, Weeks, A., additional, Smith, C. A., additional, Rutka, J. T., additional, Georges, J., additional, Samuelson, G., additional, Misra, A., additional, Joy, A., additional, Huang, Y., additional, McQuilkin, M., additional, Yoshihiro, A., additional, Carpenter, D., additional, Butler, L., additional, Feuerstein, B., additional, Murphy, S. F., additional, Vaghaiwalla, T., additional, Wotoczek-Obadia, M., additional, Albright, R., additional, Mack, D., additional, Lawn, S., additional, Henderson, F., additional, Jung, M., additional, Dakshanamurthy, S., additional, Brown, M., additional, Forsyth, P., additional, Brem, S., additional, Sadr, M. S., additional, Maret, D., additional, Sadr, E. S., additional, Siu, V., additional, Alshami, J., additional, Trinh, G., additional, Denault, J.-S., additional, Faury, D., additional, Jabado, N., additional, Nantel, A., additional, and Del Maestro, R., additional

Published
2011
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32. MEDICAL AND NEURO-ONCOLOGY

Author

Prithviraj, G. K., primary, Sommers, S. R., additional, Jump, R. L., additional, Halmos, B., additional, Chambless, L. B., additional, Parker, S. L., additional, Hassam-Malani, L., additional, McGirt, M. J., additional, Thompson, R. C., additional, Hunter, K., additional, Chamberlain, M. C., additional, Le, E. M., additional, Lee, E. L. T., additional, Sadighi, Z. S., additional, Pearlman, M. L., additional, Slopis, J. M., additional, Vats, T. S., additional, Khatua, S., additional, DeVito, N. C., additional, Yu, M., additional, Chen, R., additional, Pan, E., additional, Cloughesy, T., additional, Raizer, J., additional, Drappatz, J., additional, Gerena-Lewis, M., additional, Rogerio, J., additional, Yacoub, S., additional, Desjardin, A., additional, Groves, M. D., additional, DeGroot, J., additional, Loghin, M., additional, Conrad, C. A., additional, Hess, K., additional, Ni, J., additional, Ictech, S., additional, Yung, W. A., additional, Porter, A. B., additional, Dueck, A. C., additional, Karlin, N. J., additional, Olson, J., additional, Silber, J., additional, Reiner, A. S., additional, Panageas, K. S., additional, Iwamoto, F. M., additional, Cloughesy, T. F., additional, Aldape, K. D., additional, Rivera, A. L., additional, Eichler, A. F., additional, Louis, D. N., additional, Paleologos, N. A., additional, Fisher, B. J., additional, Ashby, L. S., additional, Cairncross, J. G., additional, Roldan, G. B., additional, Wen, P. Y., additional, Ligon, K. L., additional, Shiff, D., additional, Robins, H. I., additional, Rocque, B. G., additional, Mason, W. P., additional, Weaver, S. A., additional, Green, R. M., additional, Kamar, F. G., additional, Abrey, L. E., additional, DeAngelis, L. M., additional, Jhanwar, S. C., additional, Rosenblum, M. K., additional, Lassman, A. 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A., additional, Ganji, S., additional, DeBerardinis, R., additional, Hatanpaa, K., additional, Rakheja, D., additional, Yang, X.-L., additional, Mashimo, T., additional, Raisanen, J., additional, Madden, C., additional, Mickey, B., additional, Malloy, C., additional, Bachoo, R., additional, Choi, C., additional, Ranjan, T., additional, Yono, N., additional, Han, S. J., additional, Sun, M., additional, Berger, M. S., additional, Aghi, M., additional, Gupta, N., additional, and Parsa, A. T., additional

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