Washout of sevoflurane from the GE Avance and Amingo Carestation anesthetic machines von BRÜNNER, H. W., POHL, S., GROND, S.

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The modular nature of genetic diseases von Oti, M, Brunner, HG

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Detection of large-scale X-ray bubbles in the Milky Way halo von Predehl, P., Sunyaev, R. A., Becker, W., Brunner, H., Burenin, R., Bykov, A., Cherepashchuk, A., Chugai, N., Churazov, E., Doroshenko, V., Eismont, N., Freyberg, M., Gilfanov, M., Haberl, F., Khabibullin, I., Krivonos, R., Maitra, C., Medvedev, P., Merloni, A., Nandra, K., Nazarov, V., Pavlinsky, M., Ponti, G., Sanders, J. S., Sasaki, M., Sazonov, S., Strong, A. W., Wilms, J.

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MICROSATELLITES CAN BE MISLEADING: AN EMPIRICAL AND SIMULATION STUDY von Balloux, François, Brünner, Harald, Lugon-Moulin, Nicolas, Hausser, Jacques, Goudet, Jérôme

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Impingement Syndrome of the Shoulder von Garving, Christina, Jakob, Sascha, Bauer, Isabel, Nadjar, Rudolph, Brunner, Ulrich H

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POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome von van Reeuwijk, J, Janssen, M, van den Elzen, C, Beltran-Valero de Bernabé, D, Sabatelli, P, Merlini, L, Boon, M, Scheffer, H, Brockington, M, Muntoni, F, Huynen, M A, Verrips, A, Walsh, C A, Barth, P G, Brunner, H G, van Bokhoven, H

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Predicting disease genes using protein–protein interactions von Oti, M, Snel, B, Huynen, M A, Brunner, H G

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THE CHANDRA COSMOS LEGACY SURVEY: OVERVIEW AND POINT SOURCE CATALOG von Civano, F., Marchesi, S., Comastri, A., Urry, M. C., Elvis, M., Cappelluti, N., Puccetti, S., Brusa, M., Zamorani, G., Hasinger, G., Aldcroft, T., Alexander, D. M., Allevato, V., Brunner, H., Capak, P., Finoguenov, A., Fiore, F., Fruscione, A., Gilli, R., Glotfelty, K., Griffiths, R. E., Hao, H., Harrison, F. A., Jahnke, K., Kartaltepe, J., Karim, A., LaMassa, S. M., Lanzuisi, G., Miyaji, T., Ranalli, P., Salvato, M., Sargent, M., Scoville, N. J., Schawinski, K., Schinnerer, E., Silverman, J., Smolcic, V., Stern, D., Toft, S., Trakhenbrot, B., Treister, E., Vignali, C.

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Angiotensin II receptor antagonists von Burnier, M, Brunner, HR

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Urban Mining A Contribution to Reindustrializing the City von Brunner, Paul H.

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DETAILED SHAPE AND EVOLUTIONARY BEHAVIOR OF THE X-RAY LUMINOSITY FUNCTION OF ACTIVE GALACTIC NUCLEI von Miyaji, T., Hasinger, G., Salvato, M., Brusa, M., Cappelluti, N., Civano, F., Puccetti, S., Elvis, M., Brunner, H., Fotopoulou, S., Ueda, Y., Griffiths, R. E., Koekemoer, A. M., Akiyama, M., Comastri, A., Gilli, R., Lanzuisi, G., Merloni, A., Vignali, C.

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Verbund-Simulation - Strategic Planning and Optimization of Integrated Production Networks von Viere, T., Brünner, H., Hedemann, J.

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CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene von Jongmans, M C J, Admiraal, R J, van der Donk, K P, Vissers, L E L M, Baas, A F, Kapusta, L, van Hagen, J M, Donnai, D, de Ravel, T J, Veltman, J A, Geurts van Kessel, A, De Vries, B B A, Brunner, H G, Hoefsloot, L H, van Ravenswaaij, C M A

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Effect of B-type natriuretic peptide-guided treatment of chronic heart failure on total mortality and hospitalization: an individual patient meta-analysis von Troughton, Richard W, Frampton, Christopher M, Brunner-La Rocca, Hans-Peter, Pfisterer, Matthias, Eurlings, Luc W M, Erntell, Hans, Persson, Hans, O'Connor, Christopher M, Moertl, Deddo, Karlström, Patric, Dahlström, Ulf, Gaggin, Hanna K, Januzzi, James L, Berger, Rudolf, Richards, A Mark, Pinto, Yigal M, Nicholls, M Gary

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De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype von Roifman, M., Marcelis, C.L.M., Paton, T., Marshall, C., Silver, R., Lohr, J.L., Yntema, H.G., Venselaar, H., Kayserili, H., van Bon, B., Seaward, G., Brunner, H.G., Chitayat, D.

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CHD7 mutations in patients initially diagnosed with Kallmann syndrome - the clinical overlap with CHARGE syndrome von Jongmans, MCJ, Van Ravenswaaij-Arts, CMA, Pitteloud, N, Ogata, T, Sato, N, Claahsen-van der Grinten, HL, Van Der Donk, K, Seminara, S, Bergman, JEH, Brunner, HG, Crowley Jr, WF, Hoefsloot, LH

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Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability von Reijnders, M. R. F., Kousi, M., van Woerden, G. M., Klein, M., Bralten, J., Mancini, G. M. S., van Essen, T., Proietti-Onori, M., Smeets, E. E. J., van Gastel, M., Stegmann, A. P. A., Stevens, S. J. C., Lelieveld, S. H., Gilissen, C., Pfundt, R., Tan, P. L., Kleefstra, T., Franke, B., Elgersma, Y., Katsanis, N., Brunner, H. G.

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Use of atorvastatin in systemic lupus erythematosus in children and adolescents von Schanberg, L. E., Sandborg, C., Barnhart, H. X., Ardoin, S. P., Yow, E., Evans, G. W., Mieszkalski, K. L., Ilowite, N. T., Eberhard, A., Imundo, L. F., Kimura, Y., von Scheven, E., Silverman, E., Bowyer, S. L., Punaro, M., Singer, N. G., Sherry, D. D., McCurdy, D., Klein-Gitelman, M., Wallace, C., Silver, R., Wagner-Weiner, L., Higgins, G. C., Brunner, H. I., Jung, L., Soep, J. B., Reed, A. M., Provenzale, J., Thompson, S. D.

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CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy von Friedman, J I, Vrijenhoek, T, Markx, S, Janssen, I M, van der Vliet, W A, Faas, B H W, Knoers, N V, Cahn, W, Kahn, R S, Edelmann, L, Davis, K L, Silverman, J M, Brunner, H G, van Kessel, A Geurts, Wijmenga, C, Ophoff, R A, Veltman, J A

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Renal effects of selective cyclooxygenase-2 inhibition in normotensive salt-depleted subjects von Rossat, Julien, Maillard, Marc, Nussberger, Jürg, Brunner, Hans R., Burnier, Michel

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