A new mutation of the fukutin gene causing late-onset limb girdle muscular dystrophy von Riisager, M, Duno, M, Hansen, F. Juul, Krag, T.O, Vissing, C.R, Vissing, J

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Skeletal muscle involvement in patients with truncations of titin and familial dilated cardiomyopathy von Vissing, C R, Skriver, S V, Krett, B, Poulsen, N S, Krag, T, Walas, H R, Christensen, A H, Bundgaard, H, Vissing, J

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Subclinical myocardial phenotype in genotype-positive relatives attending clinical and genetic screening for familial dilated cardiomyopathy von Tellefsen, S, Vissing, C R, Dybro, A M, Bundgaard, H, Poulsen, S H, Jensen, M S K, Christensen, A H, Rasmussen, T B

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Long-term follow-up in patients with hypertrophic cardiomyopathy after defibrillator implantation: analysis of appropriate and inappropriate therapy von Basse Christensen, E, Vissing, C R, Silajdzija, E, Mills, H L, Thune, J J, Bosselmann, H, Larroude, C E, Philbert, B T, Raja, A A, Christensen, A H, Bundgaard, H

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Family screening in dilated cardiomyopathy-qualifying screening and need for follow-up von Vissing, C R, Espersen, K, Mills, H L, Bartels, E D, Jurlander, R, Skriver, S V, Ghouse, J, Thune, J J, Axelsson Raja, A, Christensen, A H, Bundgaard, H

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P337Natural history, reversibility and arrhythmias associated with truncating titin variants in dilated cardiomyopathy von Vissing, C R, Rasmussen, T B, Olesen, M S, Pedersen, L N, Dybro, A, Bundgaard, H, Jensen, M, Christensen, A H

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Timing of cardioverter-defibrillator implantation in patients with cardiac laminopathies—External validation of the LMNA-risk ventricular tachyarrhythmia calculator von Rootwelt-Norberg, Christine, Christensen, Alex Hørby, Skjølsvik, Eystein T., Chivulescu, Monica, Vissing, Christoffer R., Bundgaard, Henning, Aabel, Eivind W., Bogsrud, Martin P., Hasselberg, Nina E., Lie, Øyvind H., Haugaa, Kristina H.

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G.P.115 Recurrent myoglobinuria and deranged acyl-carnitines due to mutation of the COII gene of mtDNA von Vissing, C.R, Duno, M, Wibrand, F, Vissing, J

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P.5.6 Aerobic training in patients with myopathy and hyperCKemia caused by anoctamin 5 deficiency von Vissing, C.R, Preisler, N.R, Husu, E, Prahm, K.P, Vissing, J

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Left Ventricular Systolic Dysfunction in Patients Diagnosed With Hypertrophic Cardiomyopathy During Childhood: Insights From the SHaRe Registry von Abou Alaiwi, S, Roston, TM, Marstrand, P, Claggett, BL, Parikh, VN, Helms, AS, Ingles, J, Lampert, R, Lakdawala, NK, Michels, M, Owens, AT, Rossano, JW, Saberi, S, Abrams, DJ, Ashley, EA, Semsarian, C, Stendahl, JC, Ware, JS, Miller, E, Ryan, TD, Russell, MW, Day, SM, Olivotto, I, Vissing, CR, Ho, CY

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Cardiac Outcomes in Adults With Mitochondrial Diseases von Savvatis, K, Vissing, CR, Klouvi, L, Florian, A, Rahman, M, Béhin, A, Fayssoil, A, Masingue, M, Stojkovic, T, Bécane, HM, Berber, N, Mochel, F, Duboc, D, Fontaine, B, Krett, B, Stalens, C, Lejeune, J, Pitceathly, RDS, Lopes, L, Saadi, M, Gossios, T, Procaccio, V, Spinazzi, M, Tard, C, De Groote, P, Dhaenens, CM, Douillard, C, Echaniz-Laguna, A, Quinlivan, R, Hanna, MG, Yilmaz, A, Vissing, J, Laforêt, P, Elliott, P, Wahbi, K

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Results of an open label feasibility study of sodium valproate in people with McArdle disease von Scalco, RS, Stemmerik, M, Løkken, N, Vissing, CR, Madsen, KL, Michalak, Z, Pattni, J, Godfrey, R, Samandouras, G, Bassett, P, Holton, JL, Krag, T, Haller, RG, Sewry, C, Wigley, R, Vissing, J, Quinlivan, R

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The burden of severe asthma in childhood and adolescence: results from the paediatric U-BIOPRED cohorts von Fleming, Louise, Murray, Clare, Bansal, Aruna T, Hashimoto, Simone, Bisgaard, Hans, Bush, Andrew, Frey, Urs, Hedlin, Gunilla, Singer, Florian, van Aalderen, Wim M, Vissing, Nadja H, Zolkipli, Zaraquiza, Selby, Anna, Fowler, Stephen, Shaw, Dominick, Chung, Kian Fan, Sousa, Ana R, Wagers, Scott, Corfield, Julie, Pandis, Ioannis, Rowe, Anthony, Formaggio, Elena, Sterk, Peter J, Roberts, Graham

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McArdle disease: a clinical review von Quinlivan, R, Buckley, J, James, M, Twist, A, Ball, S, Duno, M, Vissing, J, Bruno, C, Cassandrini, D, Roberts, M, Winer, J, Rose, M, Sewry, C

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Treatable traits in the European U‐BIOPRED adult asthma cohorts von Simpson, Andrew J., Hekking, Pieter‐Paul, Shaw, Dominick E., Fleming, Louise J., Roberts, Graham, Riley, John H., Bates, Stewart, Sousa, Ana R., Bansal, Aruna T., Pandis, Ioannis, Sun, Kai, Bakke, Per S., Caruso, Massimo, Dahlén, Barbro, Dahlén, Sven‐Erik, Horvath, Ildiko, Krug, Norbert, Montuschi, Paolo, Sandstrom, Thomas, Singer, Florian, Adcock, Ian M., Wagers, Scott S., Djukanovic, Ratko, Chung, Kian Fan, Sterk, Peter J., Fowler, Stephen J., Ahmed, H, Auffray, C, Baribaud, F, Bel, E. H, Bisgaard, H, Bønnelykke, K, Brandsma, J, Brinkman, P, Bucchioni, E, Burg, D, Bush, A, Chaiboonchoe, A, Chanez, P, Compton, C. H, Corfield, J, D'Amico, A, De Meulder, B, Erpenbeck, V. J, Erzen, D, Fichtner, K, Fleming, L. J, Formaggio, E, Frey, U, Gahlemann, M, Geiser, T, Goss, V, Guo, Y, Hashimoto, S, Haughney, J, Hedlin, G, Hekking, P. W, Higenbottam, T, Hohlfeld, J. M, Holweg, C, Horváth, I, Howarth, P, James, A. J, Knowles, R, Knox, A. J, Lefaudeux, D, Lutter, R, Manta, A, Masefield, S, Matthews, J. G, Mazein, A, Meiser, A, Middelveld, R. J. M, Miralpeix, M, Mores, N, Murray, C. S, Myles, D, Pahus, L, Pavlidis, S, Postle, A, Powel, P, Praticò, G, Rao, N, Roberts, A, Roberts, G, Rowe, A, Sandström, T, Schofield, J. P. R, Selby, A, Sigmund, R, Skipp, P. J, Thornton, B, Aalderen, W. M, Geest, M, Vestbo, J, Vissing, N. H, Wagener, A. H, Weiszhart, Z, Wheelock, C. E, Wilson, S. J

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Tranexamic Acid Decreases Incidence of Blood Transfusion in Simultaneous Bilateral Total Knee Arthroplasty von Bagsby, Deren T., MD, Samujh, Christopher A., MD, Vissing, Jacqueline L., BS, Empson, Janene A., RN, ONC, Pomeroy, Donald L., MD, Malkani, Arthur L., MD

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Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N‐related myopathies von Bachmann, Christoph, Noreen, Faiza, Voermans, Nicol C., Schär, Primo L., Vissing, John, Fock, Johanna M., Bulk, Saskia, Kusters, Benno, Moore, Steven A., Beggs, Alan H., Mathews, Katherine D., Meyer, Megan, Genetti, Casie A., Meola, Giovanni, Cardani, Rosanna, Mathews, Emma, Jungbluth, Heinz, Muntoni, Francesco, Zorzato, Francesco, Treves, Susan

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A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy von Vissing, John, Barresi, Rita, Witting, Nanna, Van Ghelue, Marijke, Gammelgaard, Lise, Bindoff, Laurence A, Straub, Volker, Lochmüller, Hanns, Hudson, Judith, Wahl, Christoph M, Arnardottir, Snjolaug, Dahlbom, Kathe, Jonsrud, Christoffer, Duno, Morten

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European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10‐year experience von Ploeg, A. T., Kruijshaar, M. E., Toscano, A., Laforêt, P., Angelini, C., Lachmann, R. H., Pascual Pascual, S. I., Roberts, M., Rösler, K., Stulnig, T., Doorn, P. A., Van den Bergh, P. Y. K., Vissing, J., Schoser, B., Bembi, Bruno, Broomfield, Alexander, Boentert, Matthias, Desnuelle, Claude, Findling, Oliver, Hahn, Andreas, Díaz‐Manera, Jordi, Hundsberger, Thomas, Kornblum, Cornelia, Labarthé, Franҫois, Laforet, Pascal, Mengel, Karl‐Eugen, Mongini, Tiziana, Muller‐Felber, Wolfgang, Parenti, Giancarlo, Pijnappel, W. Pim, Preisler, Nicolai, Sacconi, Sabrina, Talim, Beril, Tardieu, Marine, Beek, Nadine A.M.E, Wenninger, Stephan

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Asthma and Wheeze Severity and the Oropharyngeal Microbiota in Children and Adolescents von Thorsen, Jonathan, Stokholm, Jakob, Rasmussen, Morten Arendt, Roggenbuck-Wedemeyer, Michael, Vissing, Nadja H, Mortensen, Martin S, Brejnrod, Asker D, Fleming, Louise, Bush, Andrew, Roberts, Graham, Singer, Florian, Frey, Urs, Hedlin, Gunilla, Nordlund, Björn, Murray, Clare S, Abdel-Aziz, Mahmoud I, Hashimoto, Simone, van Aalderen, Wim, Maitland-van der Zee, Anke H, Shaw, Dominick, Fowler, Stephen J, Sousa, Ana, Sterk, Peter J, Chung, Kian Fan, Adcock, Ian M, Djukanovic, Ratko, Auffray, Charles, Bansal, Aruna T, Wagers, Scott, Chawes, Bo, Bønnelykke, Klaus, Sørensen, Søren Johannes, Bisgaard, Hans

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