Search Results - Zwarts, KY

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  1. 1
    Desmin-related myopathy

    Desmin-related myopathy by van Spaendonck-Zwarts, KY, van Hessem, L, Jongbloed, JDH, de Walle, HEK, Capetanaki, Y, van der Kooi, AJ, van Langen, IM, van den Berg, MP, van Tintelen, JP

    Published in Clinical genetics
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  2. 2
    RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling

    RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling by van den Hoogenhof, Maarten M.G, Beqqali, Abdelaziz, Amin, Ahmad S, van der Made, Ingeborg, Aufiero, Simona, Khan, Mohsin A.F, Schumacher, Cees A, Jansweijer, Joeri A, van Spaendonck-Zwarts, Karin Y, Remme, Carol Ann, Backs, Johannes, Verkerk, Arie O, Baartscheer, Antonius, Pinto, Yigal M, Creemers, Esther E

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  3. 3
    Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease

    Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease by CLEE, Susanne M, ZWINDERMAN, Aeilko H, BROOKS-WILSON, Angela, GENEST, Jacques JR, KASTELEIN, John J. P, HAYDEN, Michael R, ENGERT, James C, ZWARTS, Karin Y, MOLHUIZEN, Henri O. F, ROOMP, Kirsten, JUKEMA, J. Wouter, VAN WIJLAND, Michel, VAN DAM, Marjel, HUDSON, Thomas J

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  4. 4
    Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes

    Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes by Clee, S M, Kastelein, J J, van Dam, M, Marcil, M, Roomp, K, Zwarts, K Y, Collins, J A, Roelants, R, Tamasawa, N, Stulc, T, Suda, T, Ceska, R, Boucher, B, Rondeau, C, DeSouich, C, Brooks-Wilson, A, Molhuizen, H O, Frohlich, J, Genest, Jr, J, Hayden, M R

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  5. 5
    Renal cancer and pneumothorax risk in Birt―Hogg―Dubé syndrome; an analysis of II5 FLCN mutation carriers from 35 BHD families

    Renal cancer and pneumothorax risk in Birt―Hogg―Dubé syndrome; an analysis of II5 FLCN mutation carriers from 35 BHD families by HOUWELING, A. C, GIJEZEN, L. M, DE JONG, M. M, BONGERS, Emhf, JOHANNESMA, P. C, POSTMUS, P. E, VAN MOORSELAAR, Rja, VAN WAESBERGHE, J-Htm, STARINK, T. M, STEENSEL, Mam Van, GILLE, Jjp, MENKO, F. H, JONKER, M. A, VAN DOORN, Mba, OLDENBURG, R. A, SPAENDONCK-ZWARTS, Ky Van, LETER, E. M, OS, Ta Van, GRIEKEN, Nct Van, JASPARS, E. H

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  6. 6
    ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels

    ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels by Zwarts, KY, Clee, SM, Zwinderman, AH, Engert, JC, Singaraja, R, Loubser, O, James, E, Roomp, K, Hudson, TJ, Jukema, JW, Kastelein, JJP, Hayden, MR

    Published in Clinical genetics
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