Mostrar 1 - 8 resultats de 8 per cerca 'De Visser, M', hora de la petició: 0.04sec
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Dystrophin muscle enhancer 1 is implicated in the activation of non-muscle isoforms in the skeletal muscle of patients with X-linked dilated cardiomyopathy. per Bastianutto, C, Bestard, J, Lahnakoski, K, Broere, D, De Visser, M, Zaccolo, M, Pozzan, T, Ferlini, A, Muntoni, F, Patarnello, T, Klamut, H
Publicat 2001Journal article -
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EFNS review on the role of muscle biopsy in the investigation of myalgia. per Kyriakides, T, Angelini, C, Schaefer, J, Mongini, T, Siciliano, G, Sacconi, S, Joseph, J, Burgunder, J, Bindoff, L, Vissing, J, de Visser, M, Hilton-Jones, D
Publicat 2013Journal article -
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EFNS review on the role of muscle biopsy in the investigation of myalgia per Kyriakides, T, Angelini, C, Schaefer, J, Mongini, T, Siciliano, G, Sacconi, S, Joseph, J, Burgunder, J, Bindoff, L, Vissing, J, De Visser, M, Hilton-Jones, D
Publicat 2013Journal article -
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205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28-30 March 2014, Naarden, The Netherlands. per De Bleecker, J, De Paepe, B, Aronica, E, de Visser, M, Amato, A, Aronica, E, Benveniste, O, De Bleecker, J, de Boer, O, De Paepe, B, de Visser, M, Dimachkie, M, Gherardi, R, Goebel, H, Hilton-Jones, D, Holton, J, Lundberg, I, Mammen, A, Mastaglia, F, Nishino, I, Rushing, E, Daa Schroder, H, Selcen, D, Stenzel, W
Publicat 2015Journal article -
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Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis. per Es, V, Van Vught, P, Veldink, J, Andersen, P, Birve, A, Lemmens, R, Cronin, S, Van Der Kooi, A, De Visser, M, Schelhaas, H, Hardiman, O, Ragoussis, I, Lambrechts, D, Robberecht, W, Wokke, J, Ophoff, R, Van Den Berg, L
Publicat 2009Journal article -
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NEK1 variants confer susceptibility to amyotrophic lateral sclerosis per Kenna, P, van Doormaal PTC, P, Dekker, A, Ticozzi, N, Kenna, B, Diekstra, F, van Rheenen, W, van Eijk, K, Jones, A, Keagle, P, Shatunov, A, Sproviero, W, Smith, B, van Es, M, Topp, S, Kenna, A, Miller, J, Fallini, C, Tiloca, C, McLaughlin, R, Vance, C, Troakes, C, Colombrita, C, Mora, G, Calvo, A, Verde, F, Al-Sarraj, S, King, A, Calini, D, de Belleroche, J, Baas, F, van der Kooi, A, de Visser, M, ten Asbroek, A, Sapp, P, McKenna-Yasek, D, Polak, M, Asress, S, Munoz-Blanco, J, SLAGEN Consortium, Lauria, G, Williams, K, Leigh, P, Nicholson, G, Blair, I, Leblond, C, Dion, P, Rouleau, G, Pall, H, Shaw, P, Turner, M, Talbot, K, Taroni, F, Boylan, K, Van Blitterswijk, M, Rademakers, R, Esteban-Perez, J, Garcia-Redondo, A, Van Damme, P, Robberecht, W, Chio, A, Gellera, C, Drepper, C, Sendtner, M, Ratti, A, Glass, J, Mora, J, Basak, A, Hardiman, O, Ludolph, A, Andersen, P, Wesihaupt, J, Brown, R, Al-Chalabi, A, Silani, V, Shaw, C, van den Berg, L, Veldink, J, Landers, J
Publicat 2016Journal article -
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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis per Lin, K, Pulit, SL, Van Rheenen, W, Shatunov, A, Dekker, AM, McLaughlin, RL, Diekstra, FP, Van Der Spek, RAA, Võsa, U, De Jong, S, Robinson, MR, Yang, J, Fogh, I, Van Doormaal, PT, Tazelaar, GHP, Koppers, M, Blokhuis, AM, Sproviero, W, Jones, AR, Kenna, KP, Van Eijk, KR, Harschnitz, O, Schellevis, RD, Brands, WJ, Medic, J, Menelaou, A, Vajda, A, Ticozzi, N, Rogelj, B, Vrabec, K, Ravnik-Glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Grošelj, LD, Millecamps, S, Salachas, F, Meininger, V, De Carvalho, M, Pinto, S, Mora, JS, Rojas-García, R, Polak, M, Chandran, S, Colville, S, Swingler, R, Morrison, KE, Shaw, PJ, Hardy, J, Orrell, RW, Pittman, A, Sidle, K, Fratta, P, Malaspina, A, Topp, S, Petri, S, Abdulla, S, Drepper, C, Sendtner, M, Meyer, T, Ophoff, RA, Staats, KA, Wiedau-Pazos, M, Lomen-Hoerth, C, Van Deerlin, VM, Trojanowski, JQ, Elman, L, McCluskey, L, Basak, AN, Tunca, C, Hamzeiy, H, Parman, Y, Meitinger, T, Lichtner, P, Radivojkov-Blagojevic, M, Andres, CR, Maurel, C, Bensimon, G, Landwehrmeyer, B, Brice, A, Payan, CAM, Saker-Delye, S, Dürr, A, Wood, NW, Tittmann, L, Lieb, W, Franke, A, Rietschel, M, Cichon, S, Nöthen, MM, Amouyel, P, Tzourio, C, Dartigues, J-F, Uitterlinden, AG, Rivadeneira, F, Estrada, K, Hofman, A, Curtis, C, Blauw, HM, Van Der Kooi, AJ, De Visser, M, Goris, A, Weber, M, Shaw, CE, Smith, BN, Pansarasa, O, Cereda, C, Del Bo, R, Comi, GP, D'Alfonso, S, Bertolin, C, Sorarù, G, Mazzini, L, Pensato, V, Gellera, C, Tiloca, C, Ratti, A, Calvo, A, Moglia, C, Brunetti, M, Arcuti, S, Capozzo, R, Zecca, C, Lunetta, C, Penco, S, Riva, N, Padovani, A, Filosto, M, Muller, B, Stuit, RJ, Registry, P, Slalom Group, Registry, S, Fals Sequencing Consortium, Slagen Consortium, Nnipps Study Group, Blair, I, Zhang, K, McCann, EP, Fifita, JA, Nicholson, GA, Rowe, DB, Pamphlett, R, Kiernan, MC, Grosskreutz, J, Witte, OW, Ringer, T, Prell, T, Stubendorff, B, Kurth, I, Hübner, CA, Leigh, PN, Casale, F, Chio, A, Beghi, E, Pupillo, E, Tortelli, R, Logroscino, G, Powell, J, Ludolph, AC, Weishaupt, JH, Robberecht, W, Van Damme, P, Franke, L, Pers, TH, Brown, RH, Glass, JD, Landers, JE, Hardiman, O, Andersen, PM, Corcia, P, Vourc'H, P, Silani, V, Wray, NR, Visscher, PM, De Bakker, PIW, Van Es, MA, Pasterkamp, RJ, Lewis, CM, Breen, G, Al-Chalabi, A, Van Den Berg, LH, Veldink, JH
Publicat 2016Journal article