Failure of calcitriol treatment in a patient with malignant osteopetrosis von VAN LIE PETERS, E. M, ARONSON, D. C, EVERTS, V, DOOREN, L. J

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NADH:Q1 oxidoreductase deficiency without lactic acidosis in a patient with leigh syndrome: Implications for the diagnosis of inborn errors of the respiratory chain von Wijburg, F. A., Wanders, R. J. A., Lie Peters, E. M., Vos, G. D., Loggers, H. G., Bolhuis, P. A., Herzberg, N. H., Ruitenbeek, W., Wilsem, A., Houten, R., Barth, P. G.

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Megadose methylprednisolone treatment for malignant osteopetrosis von van Lie Peters, E M, Aronson, D C, Everts, V, Dooren, L J

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NADH:Q 1 oxidoreductase deficiency without lactic acidosis in a patient with leigh syndrome: Implications for the diagnosis of inborn errors of the respiratory chain von Wijburg, F. A., Wanders, R. J. A., van Lie Peters, E. M., Vos, G. D., Loggers, H. G., Bolhuis, P. A., Herzberg, N. H., Ruitenbeek, W., van Wilsem, A., ten Houten, R., Barth, P. G.

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Chronic Airway Diseases Early Stratification (CADSET): a new ERS Clinical Research Collaboration von Agusti, Alvar, Faner, Rosa, Donaldson, Gavin, Heuvelin, Elise, Breyer-Kohansal, Robab, Melén, Erik, Maitland-van der Zee, Anke H, Vestbo, Jørgen, Allinson, James P, Vanfleteren, Lowie E G W, van den Berge, Maarten, Adcock, Ian M, Lahousse, Lies, Brusselle, Guy, Wedzicha, Jadwiga A

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Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci von Cortes, Adrian, Hadler, Johanna, Pointon, Jenny P, Robinson, Philip C, Karaderi, Tugce, Leo, Paul, Cremin, Katie, Pryce, Karena, Harris, Jessica, Lee, Seunghun, Joo, Kyung Bin, Shim, Seung-Cheol, Weisman, Michael, Ward, Michael, Zhou, Xiaodong, Garchon, Henri-Jean, Chiocchia, Gilles, Nossent, Johannes, Lie, Benedicte A, Førre, Øystein, Tuomilehto, Jaakko, Laiho, Kari, Jiang, Lei, Liu, Yu, Wu, Xin, Bradbury, Linda A, Elewaut, Dirk, Burgos-Vargas, Ruben, Stebbings, Simon, Appleton, Louise, Farrah, Claire, Lau, Jonathan, Kenna, Tony J, Haroon, Nigil, Ferreira, Manuel A, Yang, Jian, Mulero, Juan, Fernandez-Sueiro, Jose Luis, Gonzalez-Gay, Miguel A, Lopez-Larrea, Carlos, Deloukas, Panos, Donnelly, Peter, Bowness, Paul, Gafney, Karl, Gaston, Hill, Gladman, Dafna D, Rahman, Proton, Maksymowych, Walter P, Xu, Huji, Crusius, J Bart A, van der Horst-Bruinsma, Irene E, Chou, Chung-Tei, Valle-Oñate, Raphael, Romero-Sánchez, Consuelo, Hansen, Inger Myrnes, Pimentel-Santos, Fernando M, Inman, Robert D, Videm, Vibeke, Martin, Javier, Breban, Maxime, Reveille, John D, Evans, David M, Kim, Tae-Hwan, Wordsworth, Bryan Paul, Brown, Matthew A

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Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies von Lal, Dennis, Ruppert, Ann-Kathrin, Trucks, Holger, Schulz, Herbert, de Kovel, Carolien G, Kasteleijn-Nolst Trenité, Dorothée, Sonsma, Anja C M, Koeleman, Bobby P, Lindhout, Dick, Weber, Yvonne G, Lerche, Holger, Kapser, Claudia, Schankin, Christoph J, Kunz, Wolfram S, Surges, Rainer, Elger, Christian E, Gaus, Verena, Schmitz, Bettina, Helbig, Ingo, Muhle, Hiltrud, Stephani, Ulrich, Klein, Karl M, Rosenow, Felix, Neubauer, Bernd A, Reinthaler, Eva M, Zimprich, Fritz, Feucht, Martha, Møller, Rikke S, Hjalgrim, Helle, De Jonghe, Peter, Suls, Arvid, Lieb, Wolfgang, Franke, Andre, Strauch, Konstantin, Gieger, Christian, Schurmann, Claudia, Schminke, Ulf, Nürnberg, Peter, Sander, Thomas

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Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy von Lal, Dennis, Trucks, Holger, Møller, Rikke S., Hjalgrim, Helle, Koeleman, Bobby P. C., Kovel, Carolien G. F., Visscher, Frank, Weber, Yvonne G., Lerche, Holger, Becker, Felicitas, Schankin, Christoph J., Neubauer, Bernd A., Surges, Rainer, Kunz, Wolfram S., Zimprich, Fritz, Franke, Andre, Illig, Thomas, Ried, Janina S., Leu, Costin, Nürnberg, Peter, Sander, Thomas

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Investigation of GRIN2A in common epilepsy phenotypes von Lal, Dennis, Steinbrücker, Sandra, Schubert, Julian, Sander, Thomas, Becker, Felicitas, Weber, Yvonne, Lerche, Holger, Thiele, Holger, Krause, Roland, Lehesjoki, Anna-Elina, Nürnberg, Peter, Palotie, Aarno, Neubauer, Bernd A, Muhle, Hiltrud, Stephani, Ulrich, Helbig, Ingo, Becker, Albert J, Schoch, Susanne, Hansen, Jörg, Dorn, Thomas, Hohl, Christin, Lüscher, Nicole, von Spiczak, Sarah, Lemke, Johannes R

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Conjugated Equine Estrogens and Colorectal Cancer Incidence and Survival: The Women's Health Initiative Randomized Clinical Trial von RITENBAUGH, Cheryl, STANFORD, Janet L, MASON, Ellen, MCNEELEY, S. Gene, ASCENSAO, Joao, CHLEBOWSKI, Rowan T, LIELING WU, SHIKANY, James M, SCHOEN, Robert E, STEFANICK, Marcia L, TAYLOR, Vicky, GARLAND, Cedric, FRANK, Gail, LANE, Dorothy

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Kawasaki Disease: A Maturational Defect in Immune Responsiveness von Kuijpers, T. W., Wiegman, A., van Lier, R. A. W., Roos, M. T. L., Wertheim-van Dillen, P. M. E., Pinedo, S., Ottenkamp, J.

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Hyperemic coronary flow after optimized intravascular ultrasound-guided balloon angioplasty and stent implantation von van Liebergen, Rob A.M, Piek, Jan J, Koch, Karel T, Peters, Ron J.G, de Winter, Robbert J, Schotborgh, Carl E, Lie, Kong I

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Hyperemic coronary flow After optimized intravascular ultrasound-guided balloon angioplasty and stent implantation. Commentary von VAN LIEBERGEN, R. A. M, PIEK, J. J, KOCH, K. T, PETERS, R. J. G, DE WINTER, R. J, SCHOTBORGH, C. E, LIE, K. I, COLOMBO, A, BRIGUORI, C

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De Nieuwe Taalgids. Jaargang 86 von [tijdschrift] Nieuwe Taalgids, De

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