Motives and considerations regarding PGT in couples carrying a structural chromosomal abnormality: a qualitative exploration von De Krom, G., Severijns, Y., Vlieg, W. L., Arens, Y. H. J. M., Van Golde, R. J. T., De Die-Smulders, C. E. M., Van Osch, L. A. D. M.

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Lessons learned from unsolicited findings in clinical exome sequencing of 16,482 individuals von van der Schoot, Vyne, Haer-Wigman, Lonneke, Feenstra, Ilse, Tammer, Femke, Oerlemans, Anke J M, van Koolwijk, Martine P A, van Agt, Frans, Arens, Yvonne H J M, Brunner, Han G, Vissers, Lisenka E L M, Yntema, Helger G

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Improvement in exercise tolerance and symptoms of congestive heart failure during treatment with candesartan cilexetil von RIEGGER, G. A. J, BOUZO, H, PETR, P, MÜNZ, J, SPACEK, R, PETHIG, H, VON BEHREN, V, GEORGE, M, ARENS, H.-J

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Recurrent miscarriage in translocation carriers: no differences in clinical characteristics between couples who accept and couples who decline PGD von De Krom, G., Arens, Y.H.J.M., Coonen, E., Van Ravenswaaij-Arts, C.M.A., Meijer-Hoogeveen, M., Evers, J.L.H., Van Golde, R.J.T., De Die-Smulders, C.E.M.

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Reliability study of the sonographic measurement of the acromiohumeral distance in symptomatic patients von Pijls, B. G., Kok, F. P., Penning, L. I. F., Guldemond, N. A., Arens, H. J.

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Dose-finding study of candesartan cilexetil plus hydrochlorothiazide in patients with mild to moderate hypertension von Philipp, T, Letzel, H, Arens, H J

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The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes von Paulussen, Aimée DC, Schrander-Stumpel, Constance T, Tserpelis, Demis C J, Spee, Matteus K M, Stegmann, Alexander P A, Mancini, Grazia M, Brooks, Alice S, Collée, Margriet, Maat-Kievit, Anneke, Simon, Marleen E H, van Bever, Yolande, Stolte-Dijkstra, Irene, Kerstjens-Frederikse, Wilhelmina S, Herkert, Johanna C, van Essen, Anthonie J, Lichtenbelt, Klaske D, van Haeringen, Arie, Kwee, Mei L, Lachmeijer, Augusta M A, Tan-Sindhunata, Gita M B, van Maarle, Merel C, Arens, Yvonne H J M, Smeets, Eric E J G L, de Die-Smulders, Christine E, Engelen, John J M, Smeets, Hubertus J, Herbergs, Jos

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Control of the mutagenicity of aromatic amines by protein kinases and phosphatases. I. The protein phosphatase inhibitors okadaic acid and ortho-vanadate drastically reduce the mut... von OESCH-BARTLOMOWICZ, B, ARENS, H. J, RICHTER, B, HENGSTLER, J. G, OESCH, F

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Genotype-phenotype studies in three families with mutations in the polyglutamine-binding protein 1 gene (PQBP1) von Kleefstra, T, Franken, CE, Arens, YHJM, Ramakers, GJA, Yntema, HG, Sistermans, EA, Hulsmans, CFCH, Nillesen, WN, Van Bokhoven, H, De Vries, BBA, Hamel, BCJ

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Exercise related ventricular arrhythmias are related to cardiac fibrosis in hypertrophic cardiomyopathy mutation carriers von van Rijsingen, I. A. W., Bekkers, S. C. A. M., Schalla, S., Hermans-van Ast, J. F., Snoep, G., Alzand, B. S. N., Arens, Y. H. J. M., van den Wijngaard, A., Crijns, H. J. G. M., Pinto, Y. M.

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Molecular and cellular basis for adequate metabolic design of genotoxicity studies von Oesch, F., Oesch-Bartlomowicz, B., Arens, H.J., Friedberg, T., Utesch, D., Glatt, H.R., Platt, K.L.

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Subtelomeric chromosome aberrations: still a lot to learn von Moog, U, Arens, YHJM, Van Lent-Albrechts, JCM, Huijts, PEA, Smeets, EEJ, Schrander-Stumpel, CTRM, Engelen, JJM

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Hypertrophic cardiomyopathy family with double-heterozygous mutations; does disease severity suggest doubleheterozygosity? von van Rijsingen, I. A. W., Ast, J. F. Hermans-van, Arens, Y. H. J. M., Schalla, S. M., de Die-Smulders, C. E. M, van den Wijngaard, A., Pinto, Y. M.

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DIALYSIS MINERAL BONE DISEASE von Komaba, H., Taniguchi, M., Yamamoto, S., Nomura, T., Fukagawa, M., Pasch, A., De Francisco, A. L., Covic, A., Marzell, B., Arens, H. J., Passlick-Deetjen, J., Jahnen-Dechent, W., Castellano, A., Ruggiero, P., Pedrini, L. A., Barreto, F., Grassmann, A., Marcelli, D., Canaud, B., Kotanko, P., Silva, V. C., Usvyat, L., Pecoits-Filho, R., Consortium, M., Drueke, T. B., Moe, S. M., Abdalla, S., Parfrey, P. S., Chertow, G. M.

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Maturational differences between vascular and bladder smooth muscle during ovine development von Arens, Yvonne H. J. M, Rosenfeld, Charles R, Kamm, Kristine E

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Maturational differences between vascular and bladder smooth muscle during ovine development von ARENS, Y. H. J. M, ROSENFELD, C. R, KAMM, K. E

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Dialysis / Mineral bone disease 2 von Liu, F., Marzell, B., Arkossy, O., Gurevich, K., Kaufmann, P., Schoder, V., Arens, H.-J., Passlick-Deetjen, J., Bosticardo, G., Malberti, F., Basile, C., Libutti, P., Filiberti, O., Cozzolino, M., Brancaccio, D., Cannella, G., Messa, P., Mazzaferro, S., Fujii, N., Hamano, T., Taniguchi, M., Shoji, T., Shigematsu, T., Nakai, S., Iseki, K., Tsubakihara, Y.

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Long-QT mutation p.K557E-Kv7.1: dominant-negative suppression of IKs, but preserved cAMP-dependent up-regulation von Spätjens, Roel L H M G, Bébarová, Markéta, Seyen, Sandrine R M, Lentink, Viola, Jongbloed, Roselie J, Arens, Yvonne H J M, Heijman, Jordi, Volders, Paul G A

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Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers von Arens, Y.H.J.M., Engelen, J.J.M., Govaerts, L.C.P., van Ravenswaay, C.M., Loneus, W.H., van Lent-Albrechts, J.C.M., van der Blij-Philipsen, M., Hamers, A.J.H., Schrander-Stumpel, C.T.R.M.

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Comparison of ultrafast dipyridamole magnetic resonance imaging with dipyridamole sestamibi SPECT for detection of perfusion abnormalities in patients with one-vessel coronary arte... von Matheijssen, Niels A. A., Louwerenburg, Hans W., van Rugge, F. Paul, Arens, Ruud Pj. H., Kauer, Ben, de Roos, Albert, van der Wall, Ernst E.

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