Amyloid deposits and inflammatory infiltrates in sporadic inclusion body myositis: the inflammatory egg comes before the degenerative chicken by Benveniste, Olivier, Stenzel, Werner, Hilton-Jones, David, Sandri, Marco, Boyer, Olivier, van Engelen, Baziel G. M.

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The clinical spectrum of neuralgic amyotrophy in 246 cases by van Alfen, Nens, van Engelen, Baziel G. M.

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Quantitative muscle MRI and ultrasound for facioscapulohumeral muscular dystrophy: complementary imaging biomarkers by Mul, Karlien, Horlings, Corinne G. C., Vincenten, Sanne C. C., Voermans, Nicol C., van Engelen, Baziel G. M., van Alfen, Nens

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Three‐dimensional quantitative muscle ultrasound in patients with facioscapulohumeral dystrophy and myotonic dystrophy by Jong, Leon, Greco, Anna, Nikolaev, Anton, Weijers, Gert, Engelen, Baziel G. M., Korte, Chris L., Fütterer, Jurgen J.

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Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials by Stunnenberg, Bas C, Raaphorst, Joost, Groenewoud, Hans M, Statland, Jeffrey M, Griggs, Robert C, Woertman, Willem, Stegeman, Dick F, Timmermans, Janneke, Trivedi, Jaya, Matthews, Emma, Saris, Christiaan G. J, Schouwenberg, Bas J, Drost, Gea, van Engelen, Baziel G. M, van der Wilt, Gert Jan

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A 5‐year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical... by Kools, Joost, Vincenten, Sanne, Engelen, Baziel G. M., Voet, Nicoline B. M., Merkies, Ingemar, Horlings, Corinne G. C., Voermans, Nicol C., Mul, K.

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Strength training and aerobic exercise training for muscle disease by Voet, Nicoline B M, van der Kooi, Elly L, Riphagen, Ingrid I, Lindeman, Eline, van Engelen, Baziel G M, Geurts, Alexander C H

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KBTBD13 is an actin-binding protein that modulates muscle kinetics by de Winter, Josine M, Molenaar, Joery P, Yuen, Michaela, van der Pijl, Robbert, Shen, Shengyi, Conijn, Stefan, van de Locht, Martijn, Willigenburg, Menne, Bogaards, Sylvia Jp, van Kleef, Esmee Sb, Lassche, Saskia, Persson, Malin, Rassier, Dilson E, Sztal, Tamar E, Ruparelia, Avnika A, Oorschot, Viola, Ramm, Georg, Hall, Thomas E, Xiong, Zherui, Johnson, Christopher N, Li, Frank, Kiss, Balazs, Lozano-Vidal, Noelia, Boon, Reinier A, Marabita, Manuela, Nogara, Leonardo, Blaauw, Bert, Rodenburg, Richard J, Küsters, Benno, Doorduin, Jonne, Beggs, Alan H, Granzier, Henk, Campbell, Ken, Ma, Weikang, Irving, Thomas, Malfatti, Edoardo, Romero, Norma B, Bryson-Richardson, Robert J, van Engelen, Baziel Gm, Voermans, Nicol C, Ottenheijm, Coen Ac

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Distinct disease phases in muscles of facioscapulohumeral dystrophy patients identified by MR detected fat infiltration by Janssen, Barbara H, Voet, Nicoline B M, Nabuurs, Christine I, Kan, Hermien E, de Rooy, Jacky W J, Geurts, Alexander C, Padberg, George W, van Engelen, Baziel G M, Heerschap, Arend

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Myotonic dystrophy type 1: A comparison between the adult‐ and late‐onset subtype by Joosten, Isis B.T., Horlings, Corinne G. C., Vosse, Bettine A. H., Wagner, Anouk, Bovenkerk, David S. H., Evertz, Reinder, Vernooy, Kevin, Engelen, Baziel G. M., Faber, Catharina G.

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Muscle ultrasound is a sensitive biomarker in oculopharyngeal muscular dystrophy by Kroon, Rosemarie H. M. J. M., Kalf, Johanna G., Meijers, Rutger L., Swart, Bert J. M., Cameron, Ian G. M., Doorduin, Jonne, Alfen, Nens, Engelen, Baziel G. M., Horlings, Corinne G. C.

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Cognitive behavioural therapy with optional graded exercise therapy in patients with severe fatigue with myotonic dystrophy type 1: a multicentre, single-blind, randomised trial by Okkersen, Kees, Jimenez-Moreno, Cecilia, Wenninger, Stephan, Daidj, Ferroudja, Glennon, Jeffrey, Cumming, Sarah, Littleford, Roberta, Monckton, Darren G, Lochmüller, Hanns, Catt, Michael, Faber, Catharina G, Hapca, Adrian, Donnan, Peter T, Gorman, Gráinne, Bassez, Guillaume, Schoser, Benedikt, Knoop, Hans, Treweek, Shaun, van Engelen, Baziel G M, Kierkegaard, Marie, Okkersen, Kees, Jimenez-Moreno, Cecilia, Wenninger, Stephan, Daidj, Ferroudja, Glennon, Jeffrey, Cumming, Sarah, Littleford, Roberta, Monckton, Darren, Lochmüller, Hanns, Catt, Michael, Faber, Catharina, Hapca, Adrian, Donnan, Peter, Gorman, Gráinne, Bassez, Guillaume, Schoser, Benedikt, Knoop, Hans, Treweek, Shaun, van Engelen, Baziel, Maas, Daphne, Nikolaus, Stephanie, Cornelissen, Yvonne, van Nimwegen, Marlies, Klerks, Ellen, Bouman, Sacha, Heskamp, Linda, Heerschap, Arend, Rahmadi, Ridho, Groot, Perry, Heskes, Tom, Kapusta, Katarzyna, Abghari, Shaghayegh, Aschrafi, Armaz, Poelmans, Geert, Raaphorst, Joost, Trenell, Michael, van Laar, Sandra, Wood, Libby, Cassidy, Sophie, Newman, Jane, Charman, Sarah, Steffaneti, Renae, Taylor, Louise, Brownrigg, Allan, Day, Sharon, Atalaya, Antonio, Hogarth, Fiona, Schüller, Angela, Stahl, Kristina, Künzel, Heike, Wolf, Martin, Jelinek, Anna, Lignier, Baptiste, Couppey, Florence, Delmas, Stéphanie, Deux, Jean-François, Hankiewicz, Karolina, Dogan, Celine, Minier, Lisa, Chevalier, Pascale, Hamadouche, Amira, Adam, Berit, Hannah, Michael, McKenzie, Emma, Rauchhaus, Petra, Van Hees, Vincent, Catt, Sharon, Schwalber, Ameli, Merkies, Ingemar, Dittrich, Juliane

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The other face of facioscapulohumeral muscular dystrophy: Exploring orofacial weakness using muscle ultrasound by Vincenten, Sanne C. C., van Doorn, Jeroen L. M., Teeselink, Sjan, Rasing, Nathaniel B., Padberg, George W., Voermans, Nicol C., Engelen, Baziel G. M., van Alfen, Nens, Mul, Karlien

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Quantitative muscle analysis in facioscapulohumeral muscular dystrophy using whole‐body fat‐referenced MRI: Protocol development, multicenter feasibility, and repeatability by Widholm, Per, Ahlgren, André, Karlsson, Markus, Romu, Thobias, Tawil, Rabi, Wagner, Kathryn R., Statland, Jeffrey M., Wang, Leo H., Shieh, Perry B., Engelen, Baziel G. M., Cadavid, Diego, Ronco, Lucienne, Odueyungbo, Adefowope O., Jiang, John G., Mellion, Michelle L., Dahlqvist Leinhard, Olof

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Autoantibodies to cytosolic 5′-nucleotidase 1A in inclusion body myositis by Pluk, Helma, van Hoeve, Bas J. A., van Dooren, Sander H. J., Stammen-Vogelzangs, Judith, van der Heijden, Annemarie, Schelhaas, Helenius J., Verbeek, Marcel M., Badrising, Umesh A., Arnardottir, Snjolaug, Gheorghe, Karina, Lundberg, Ingrid E., Boelens, Wilbert C., van Engelen, Baziel G., Pruijn, Ger J. M.

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Pain in Ehlers-Danlos Syndrome Is Common, Severe, and Associated with Functional Impairment by Voermans, Nicol C., MD, Knoop, Hans, PhD, Bleijenberg, Gijs, PhD, van Engelen, Baziel G., MD, PhD

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Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy with Cores by Sambuughin, Nyamkhishig, Yau, Kyle S., Olivé, Montse, Duff, Rachael M., Bayarsaikhan, Munkhuu, Lu, Shajia, Gonzalez-Mera, Laura, Sivadorai, Padma, Nowak, Kristen J., Ravenscroft, Gianina, Mastaglia, Frank L., North, Kathryn N., Ilkovski, Biljana, Kremer, Hannie, Lammens, Martin, van Engelen, Baziel G.M., Fabian, Vicki, Lamont, Phillipa, Davis, Mark R., Laing, Nigel G., Goldfarb, Lev G.

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Guidelines on clinical presentation and management of nondystrophic myotonias by Stunnenberg, Bas C., LoRusso, Samantha, Arnold, W. David, Barohn, Richard J., Cannon, Stephen C., Fontaine, Bertrand, Griggs, Robert C., Hanna, Michael G., Matthews, Emma, Meola, Giovanni, Sansone, Valeria A., Trivedi, Jaya R., van Engelen, Baziel G.M., Vicart, Savine, Statland, Jeffrey M.

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Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients by Demirdas, S., Dulfer, E., Robert, L., Kempers, M., van Beek, D., Micha, D., van Engelen, B.G., Hamel, B., Schalkwijk, J., Loeys, B., Maugeri, A., Voermans, N.C.

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Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD by Krom, Yvonne D, Thijssen, Peter E, Young, Janet M, den Hamer, Bianca, Balog, Judit, Yao, Zizhen, Maves, Lisa, Snider, Lauren, Knopp, Paul, Zammit, Peter S, Rijkers, Tonnie, van Engelen, Baziel G M, Padberg, George W, Frants, Rune R, Tawil, Rabi, Tapscott, Stephen J, van der Maarel, Silvère M

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