Sigmoid cancer versus chronic diverticular disease: differentiating features at CT colonography von Lips, Leonie M J, Cremers, Pierre T J, Pickhardt, Perry J, Cremers, Simone E H, Janssen-Heijnen, Maryska L G, de Witte, Marcel T, Simons, Petra C G

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SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma von Hao, Huai-Xiang, Khalimonchuk, Oleh, Schraders, Margit, Dephoure, Noah, Bayley, Jean-Pierre, Kunst, Henricus, Devilee, Peter, Cremers, Cor W.R.J, Schiffman, Joshua D, Bentz, Brandon G, Gygi, Steven P, Winge, Dennis R, Kremer, Hannie, Rutter, Jared

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SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma von Bayley, Jean-Pierre, Dr, Kunst, Henricus PM, MD, Cascon, Alberto, PhD, Sampietro, Maria Lourdes, PhD, Gaal, José, MD, Korpershoek, Esther, BSc, Hinojar-Gutierrez, Adolfo, MD, Timmers, Henri JLM, MD, Hoefsloot, Lies H, PhD, Hermsen, Mario A, PhD, Suárez, Carlos, Prof, Hussain, A Karim, Ing, Vriends, Annette HJT, MD, Hes, Frederik J, MD, Jansen, Jeroen C, MD, Tops, Carli M, PhD, Corssmit, Eleonora P, MD, de Knijff, Peter, Prof, Lenders, Jacques WM, Prof, Cremers, Cor WRJ, Prof, Devilee, Peter, Prof, Dinjens, Winand NM, PhD, de Krijger, Ronald R, MD, Robledo, Mercedes, PhD

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SDHAF2 (PGL2-SDH5) and Hereditary Head and Neck Paraganglioma von KUNST, Henricus P. M, RUTTEN, Martijn H, DE MÖNNINK, Jan-Pieter, HOEFSLOOT, Lies H, TIMMERS, Henri J. L. M, MARRES, Henri A. M, JANSEN, Jeroen C, KREMER, Hannie, BAYLEY, Jean-Pierre, CREMERS, Cor W. R. J

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Implementation of erythroid lineage analysis by flow cytometry in diagnostic models for myelodysplastic syndromes von Cremers, Eline M P, Westers, Theresia M, Alhan, Canan, Cali, Claudia, Visser-Wisselaar, Heleen A, Chitu, Dana A, van der Velden, Vincent H J, Te Marvelde, Jeroen G, Klein, Saskia K, Muus, Petra, Vellenga, Edo, de Greef, Georgina E, Legdeur, Marie-Cecile C J C, Wijermans, Pierre W, Stevens-Kroef, Marian J P L, Silva-Coelho, Pedro da, Jansen, Joop H, Ossenkoppele, Gert J, van de Loosdrecht, Arjan A

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Adherence to Antihypertensive Treatment and the Blood Pressure–Lowering Effects of Renal Denervation in the Renal Denervation for Hypertension (DENERHTN) Trial von Azizi, Michel, Pereira, Helena, Hamdidouche, Idir, Gosse, Philippe, Monge, Matthieu, Bobrie, Guillaume, Delsart, Pascal, Mounier-Véhier, Claire, Courand, Pierre-Yves, Lantelme, Pierre, Denolle, Thierry, Dourmap-Collas, Caroline, Girerd, Xavier, Michel Halimi, Jean, Zannad, Faiez, Ormezzano, Olivier, Vaïsse, Bernard, Herpin, Daniel, Ribstein, Jean, Chamontin, Bernard, Mourad, Jean-Jacques, Ferrari, Emile, Plouin, Pierre-François, Jullien, Vincent, Sapoval, Marc, Chatellier, Gilles

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Genomic array as compared to karyotyping in myelodysplastic syndromes in a prospective clinical trial von Stevens‐Kroef, Marian J., Olde Weghuis, Daniel, ElIdrissi‐Zaynoun, Najat, van der Reijden, Bert, Cremers, Eline M. P., Alhan, Canan, Westers, Theresia M., Visser‐Wisselaar, Heleen A., Chitu, Dana A., Cunha, Sonia M., Vellenga, Edo, Klein, Saskia K., Wijermans, Pierre, de Greef, Georgine E., Schaafsma, M. Ron, Muus, Petra, Ossenkoppele, Gert J., van de Loosdrecht, Arjan A., Jansen, Joop H.

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A Novel Ribosomal S6-Kinase (RSK4; RPS6KA6) Is Commonly Deleted in Patients with Complex X-Linked Mental Retardation von Yntema, Helger G., van den Helm, Bellinda, Kissing, Johan, van Duijnhoven, Gerard, Poppelaars, Francis, Chelly, Jamel, Moraine, Claude, Fryns, Jean-Pierre, Hamel, Ben C.J., Heilbronner, Helmut, Pander, Hans-Jürgen, Brunner, Han G., Ropers, Hans-Hilger, Cremers, Frans P.M., van Bokhoven, Hans

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Abdominal Aortic Calcifications Influences the Systemic and Renal Hemodynamic Response to Renal Denervation in the DENERHTN (Renal Denervation for Hypertension) Trial von Courand, Pierre‐Yves, Pereira, Helena, Del Giudice, Costantino, Gosse, Philippe, Monge, Matthieu, Bobrie, Guillaume, Delsart, Pascal, Mounier‐Vehier, Claire, Lantelme, Pierre, Denolle, Thierry, Dourmap, Caroline, Halimi, Jean Michel, Girerd, Xavier, Rossignol, Patrick, Zannad, Faiez, Herpin, Daniel, Ribstein, Jean, Bouhanick, Beatrice, Mourad, Jean‐Jacques, Ferrari, Emile, Chatellier, Gilles, Sapoval, Marc, Azarine, Arshid, Azizi, Michel, Amar, L., Bobrie, G., Lorthioir, A., Lorthioir, A., Monge, M., Pagny, J.‐Y., Pagny, J.‐Y., Plouin, P. F., Plouin, P. F., Sapoval, M., Claisse, G., Delsart, P., Midulla, M., Midulla, M., Mounier‐Vehier, C., Courand, P. Y., Dauphin, R., Dauphin, R., Fauvel, J. P., Fauvel, J. P., Lantelme, P., Rouvière, O., Rouvière, O., Cremer, A., Gosse, P., Grenier, N., Lebras, Y., Lebras, Y., Trillaud, H., Trillaud, H., Dourmap‐Collas, C., Dourmap‐Collas, C., Heautot, J. F., Heautot, J. F., Larralde, A., Larralde, A., Paillard, F., Paillard, F., Cluzel, P., Girerd, X., Rosenbaum, D., Halimi, J. M., Claudon, M., Popovic, B., Rossignol, P., Zannad, F., Baguet, J. P., Ormezzano, O., Thony, F., Bartoli, J. M., Vaïsse, B., Drouineau, J., Herpin, D., Sosner, P., Tasu, J. P., Velasco, S., Ribstein, J., Kovacsik, H., Bouhanick, B., Chamontin, B., Rousseau, H., Le Jeune, S., Lopez‐Sublet, M., Mourad, J. J., Bellmann, L., Esnault, V., Ferrari, E., Sapoval, M., Bobrie, G., Chatellier, G., Zannad, F., Baguet, J. P., Kovacsik, H., Durand‐Zaleski, I., Beregi, J. P., Persu, A.

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Cohort Profile Update: The Swiss Inflammatory Bowel Disease Cohort Study (SIBDCS) von Pittet, Valérie, Michetti, Pierre, Mueller, Christoph, Braegger, Christian P, von Känel, Roland, Schoepfer, Alain, Macpherson, Andrew J, Rogler, Gerhard

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Genetic polymorphisms associated with smoking behaviour predict the risk of surgery in patients with Crohn's disease von Biedermann, L., Vallière, C., Schuurmans, M., Begré, S., Zeitz, J., Scharl, M., Schreiner, P., Kuntzen, T., Vavricka, S. R., Bauerfeind, Peter, Beglinger, Christoph, Begré, Stefan, Bengoa, José M., Biedermann, Luc, Blattmann, Mirjam, Boehm, Stephan, Braegger, Christian P., Bühr, Patrick, Burri, Emanuel, Doerig, Christopher, Dora, Barbara, Dorta, Gian, Egger, Mara, Ehmann, Tobias, Fliegner, Markus, Fraga, Montserrat, Frei, Pascal, Furlano, Raoul Ivano, Geyer, Martin, Girardin, Marc, Grandinetti, Tanja, Gysi, Beat, Haarer, Johannes, Helbling, Beat, Hengstler, Peter, Herzog, Denise, Hinterleitner, Thomas, Hiroz, Philippe, Jost, Res, Juillerat, Pascal, Knellwolf, Christina, Knoblauch, Christoph, Koller, Rebekka, Kullak‐Ublick, Gerd, Landolt, Markus, Macpherson, Andrew, Maerten, Philippe, Manser, Christine, Manz, Michael, Matter, Christoph, McLin, Valérie, Mendanova, Martina, Meyenberger, Christa, Michetti, Pierre, Mosler, Patrick, Mottet, Christian, Müller, Christoph, Münger‐Beyeler, Claudia, Musso, Leilla, Nagy, Andreas, Neagu, Michaela, Niess, Jan, Noël, Natacha, Nydegger, Andreas, Obialo, Nicole, Peter, Ueli, Peternac, Daniel, Piccoli‐Gfeller, Franziska, Pilz, Julia Beatrice, Restellini, Sophie, Richterich, Jean‐Pierre, Rihs, Sylvia, Ritz, Marc Alain, Rogler, Daniela, Rogler, Gerhard, Rossel, Jean‐Benoît, Sagmeister, Markus, Sauter, Bernhard, Sawatzki, Mikael, Schelling, Martin, Uebelhart, Sybille Schmid, Schoepfer, Alain, Seibold, Frank, Senning, Arne, Sokollik, Christiane, Spalinger, Johannes, Steuerwald, Michael, Straumann‐Funk, Bigna, Sulz, Michael, Thorens, Joël, Tutuian, Radu, Vavricka, Stephan, Von Känel, Roland, Vonlaufen, Alain, Vulliamy, Rachel, Wermuth, Jürg, Werner, Helene, Wiesel, Paul, Wiest, Reiner, Zimmermann, Dorothee

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LF 16.0335, a novel potent and selective nonpeptide antagonist of the human bradykinin B 2 receptor von Pruneau, Didier, Luccarini, Jean‐Michel, Fouchet, Chantal, Defrêne, Evelyne, Franck, Rose‐Marie, Loillier, Bruno, Duclos, Hervé, Robert, Claude, Cremers, Béatrice, Bélichard, Pierre, Paquet, Jean‐Luc

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NH2- and COOH-Terminal Truncations of Murine Granulocyte Chemotactic Protein-2 Augment the In Vitro and In Vivo Neutrophil Chemotactic Potency von Wuyts, Anja, D'Haese, Anne, Cremers, Valerie, Menten, Patricia, Lenaerts, Jean-Pierre, De Loof, Arnold, Heremans, Hubertine, Proost, Paul, Van Damme, Jo

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Session-state Reveal Is Stronger Than Ephemeral Key Reveal: Attacking the NAXOS Authenticated Key Exchange Protocol von Cremers, Cas J. F.

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Erythroid Lineage Analysis By Flow Cytometry Is of Highly Additive Value for MDS Diagnosis: A Study on Behalf of the HOVON89 Study Group von Cremers, Eline MP, Westers, Theresia M, Alhan, Canan, Cali, Claudia, Visser-Wisselaar, Heleen A, Chitu, Dana A, Stevens-Kroef, Marian JPL, Silva Coelho, Pedro, Vellenga, Edo, Klein, Saskia K., Wijermans, Pierre W., De Greef, Georgine E, Legdeur, Marie-Cecile, Muus, Petra, Ossenkoppele, Gert J, Jansen, Joop H, Van de Loosdrecht, Arjan A

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Identification Of Chromosomal Abnormalities By Microarray-Based Genomic Profiling As Compared To Karyotyping In Patients With Low and Intermediate-1 Risk Myelodysplastic Syndromes... von Stevens-Kroef, Marian J.P.L., Simons, Annet, El Idrissi-Zaynoun, Najat, van der Reijden, Bert A., Cremers, Eline M.P., Alhan, Canan, Westers, Theresia M., Visser-Wisselaar, Heleen A., Chitu, Dana, Vellenga, Edo, Klein, S.K., Wijermans, Pierre W., De Greef, Georgine E., Schaafsma, Martyn R., van Marwijk Kooy, M., Muus, Petra, Ossenkoppele, Gert J., van de Loosdrecht, Arjan A., Jansen, Joop H.

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Validation Of a Multi-Diagnostic Approach Including Flow Cytometry To Identify Specific Risk Categories Within Low and Intermediate-1 Risk Myelodysplastic Syndromes Within a Prospe... von Cremers, Eline M.P., Westers, Theresia M., Alhan, Canan, Cali, Claudia, Visser-Wisselaar, Heleen A., Chitu, Dana A, Stevens-Kroef, Marian J.P.L., Coelho, Pedro Silva, Vellenga, Edo, Klein, Saskia K., Wijermans, Pierre W., de Greef, Georgine E., Schaafsma, Martijn R., Kooy, M Marwijk, Muus, Petra, Ossenkoppele, Gert J., Jansen, Joop H., van de Loosdrecht, Arjan A.

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Longitudinal Phenotypic Analysis in Patients with Connexin 26 (GJB2) (DFNB1) and Connexin 30 (GJB6) Mutations von Stinckens, Christel, Kremer, Hannie, van Wijk, Erwin, Standaert, Lieve, Hoefsloot, Lies H., Fryns, Jean Pierre, Huygen, Patrick L. M., Cremers, Cor W. R. J.

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Bedside adherence to clinical practice guidelines in the intensive care unit: the TECLA study von Quenot, Jean-Pierre, Mentec, Hervé, Feihl, François, Annane, Djillali, Melot, Christian, Vignon, Philippe, Brun-Buisson, Christian

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Congenital aural atresia in 18q deletion or de Grouchy syndrome von NUIJTEN, Inge, ADMIRAAL, Ronald, VAN BUGGENHOUT, Griet, CREMERS, Cor, FRIJNS, Jean-Pierre, SMEETS, Dominique, VAN RAVENSWAAIJ-ARTS, Conny

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