Epidemiology of myasthenia gravis with anti‐muscle specific kinase antibodies in the Netherlands

Tekijä Niks, Erik H, Kuks, Jan B M, Verschuuren, Jan J G M
Julkaistu 2007

Multi‐parametric MR in Becker muscular dystrophy patients

Tekijä Hooijmans, Melissa T., Froeling, Martijn, Koeks, Zaida, Verschuuren, Jan J.G.M., Webb, Andrew, Niks, Erik H., Kan, Hermien E.
Julkaisussa NMR Biomed (2020)

Decision-Making And Selection Bias in Four Observational Studies on Duchenne and Becker Muscular Dystrophy

Tekijä Naarding, Karin J., Doorenweerd, Nathalie, Koeks, Zaïda, Hendriksen, Ruben G.F., Chotkan, Kinita A., Krom, Yvonne D., de Groot, Imelda J.M., Straathof, Chiara S., Niks, Erik H., Kan, Hermien E.
Julkaisussa J Neuromuscul Dis (2020)

Age-Related Longitudinal Changes in Metabolic Energy Expenditure during Walking in Boys with Duchenne Muscular Dystrophy

Tekijä Brehm, Merel-Anne, Kempen, Jiska C. E., van der Kooi, Anneke J., de Groot, Imelda J. M., van den Bergen, Janneke C., Verschuuren, Jan J. G. M., Niks, Erik H., Harlaar, Jaap
Julkaisussa PLoS One (2014)

T(2) relaxation‐time mapping in healthy and diseased skeletal muscle using extended phase graph algorithms

Tekijä Keene, Kevin R., Beenakker, Jan‐Willem M., Hooijmans, Melissa T., Naarding, Karin J., Niks, Erik H., Otto, Louise A. M., van der Pol, W. Ludo, Tannemaat, Martijn R., Kan, Hermien E., Froeling, Martijn
Julkaisussa Magn Reson Med (2020)

The Effect of Plasma From Muscle-Specific Tyrosine Kinase Myasthenia Patients on Regenerating Endplates

Tekijä ter Beek, W. Pascale, Martínez-Martínez, Pilar, Losen, Mario, de Baets, Marc H., Wintzen, Axel R., Verschuuren, Jan J.G.M., Niks, Erik H., van Duinen, Sjoerd G., Vincent, Angela, Molenaar, Peter C.
Julkaistu 2009

MRI vastus lateralis fat fraction predicts loss of ambulation in Duchenne muscular dystrophy

Tekijä Naarding, Karin J., Reyngoudt, Harmen, van Zwet, Erik W., Hooijmans, Melissa T., Tian, Cuixia, Rybalsky, Irina, Shellenbarger, Karen C., Le Louër, Julien, Wong, Brenda L., Carlier, Pierre G., Kan, Hermien E., Niks, Erik H.
Julkaisussa Neurology (2020)

MuSK IgG4 autoantibodies cause myasthenia gravis by inhibiting binding between MuSK and Lrp4

Tekijä Huijbers, Maartje G., Zhang, Wei, Klooster, Rinse, Niks, Erik H., Friese, Matthew B., Straasheijm, Kirsten R., Thijssen, Peter E., Vrolijk, Hans, Plomp, Jaap J., Vogels, Pauline, Losen, Mario, Van der Maarel, Silvère M., Burden, Steven J., Verschuuren, Jan J.
Julkaistu 2013

Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy

Tekijä Doorenweerd, Nathalie, Mahfouz, Ahmed, van Putten, Maaike, Kaliyaperumal, Rajaram, t’ Hoen, Peter A. C., Hendriksen, Jos G. M., Aartsma-Rus, Annemieke M., Verschuuren, Jan J. G. M., Niks, Erik H., Reinders, Marcel J. T., Kan, Hermien E., Lelieveldt, Boudewijn P. F.
Julkaisussa Sci Rep (2017)

Author Correction: Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy

Tekijä Doorenweerd, Nathalie, Mahfouz, Ahmed, van Putten, Maaike, Kaliyaperumal, Rajaram, t’ Hoen, Peter A. C., Hendriksen, Jos G. M., Aartsma-Rus, Annemieke M., Verschuuren, Jan J. G. M., Niks, Erik H., Reinders, Marcel J. T., Kan, Hermien E., Lelieveldt, Boudewijn P. F.
Julkaisussa Sci Rep (2018)

Preserved thenar muscles in non‐ambulant Duchenne muscular dystrophy patients

Tekijä Naarding, Karin J., Keene, Kevin R., Sardjoe Mishre, Aashley S.D., Veeger, Thom T.J., van de Velde, Nienke M., Prins, Arina J., Burakiewicz, Jedrzej, Verschuuren, Jan J.G.M., van der Holst, Menno, Niks, Erik H., Kan, Hermien E.
Julkaisussa J Cachexia Sarcopenia Muscle (2021)

Tracking disease progression non‐invasively in Duchenne and Becker muscular dystrophies

Tekijä Spitali, Pietro, Hettne, Kristina, Tsonaka, Roula, Charrout, Mohammed, van den Bergen, Janneke, Koeks, Zaïda, Kan, Hermien E., Hooijmans, Melissa T., Roos, Andreas, Straub, Volker, Muntoni, Francesco, Al‐Khalili‐Szigyarto, Cristina, Koel‐Simmelink, Marleen J.A., Teunissen, Charlotte E., Lochmüller, Hanns, Niks, Erik H., Aartsma‐Rus, Annemieke
Julkaisussa J Cachexia Sarcopenia Muscle (2018)

TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy

Tekijä Spitali, Pietro, Zaharieva, Irina, Bohringer, Stefan, Hiller, Monika, Chaouch, Amina, Roos, Andreas, Scotton, Chiara, Claustres, Mireille, Bello, Luca, McDonald, Craig M., Hoffman, Eric P., Koeks, Zaida, Eka Suchiman, H., Cirak, Sebahattin, Scoto, Mariacristina, Reza, Mojgan, ‘t Hoen, Peter A. C., Niks, Erik H., Tuffery-Giraud, Sylvie, Lochmüller, Hanns, Ferlini, Alessandra, Muntoni, Francesco, Aartsma-Rus, Annemieke
Julkaisussa Eur J Hum Genet (2020)

Risk for Myasthenia Gravis maps to (151)Pro→ Ala change in TNIP1 and to HLA-B*08

Tekijä Gregersen, Peter K., Kosoy, Roman, Lee, Annette T., Lamb, Janine, Sussman, Jon, McKee, David, Simpfendorfer, Kim R., Pirskanen-Matell, Ritva, Piehl, Frederik, Pan-Hammarstrom, Qiang, Verschuuren, J.J.G.M., Titulaer, Maarten J., Niks, Erik H., Marx, Alexander, Ströbel, Philipp, Tackenberg, Björn, Pütz, Michael, Maniaol, Angelina, Elsais, Ahmed, Tallaksen, Chantal, Harbo, Hanne. F., Lie, Benedicte A., Raychaudhuri, Soumya, de Bakker, Paul I.W., Melms, Arthur, Garchon, Henri-Jean, Willcox, Nicholas, Hammarstrom, Lennart, Seldin, Michael F.
Julkaistu 2012

Correction: The landscape of epilepsy-related GATOR1 variants

Tekijä Baldassari, Sara, Picard, Fabienne, Verbeek, Nienke E., van Kempen, Marjan, Brilstra, Eva H., Lesca, Gaetan, Conti, Valerio, Guerrini, Renzo, Bisulli, Francesca, Licchetta, Laura, Pippucci, Tommaso, Tinuper, Paolo, Hirsch, Edouard, de Saint Martin, Anne, Chelly, Jamel, Rudolf, Gabrielle, Chipaux, Mathilde, Ferrand-Sorbets, Sarah, Dorfmüller, Georg, Sisodiya, Sanjay, Balestrini, Simona, Schoeler, Natasha, Hernandez-Hernandez, Laura, Krithika, S., Oegema, Renske, Hagebeuk, Eveline, Gunning, Boudewijn, Deckers, Charles, Berghuis, Bianca, Wegner, Ilse, Niks, Erik H., Jansen, Floor E., Braun, Kees, de Jong, Daniëlle, Rubboli, Guido, Talvik, Inga, Sander, Valentin, Uldall, Peter, Jacquemont, Marie-Line, Nava, Caroline, Leguern, Eric, Julia, Sophie, Gambardella, Antonio, d’Orsi, Giuseppe, Crichiutti, Giovanni, Faivre, Laurence, Darmency, Veronique, Benova, Barbora, Krsek, Pavel, Biraben, Arnaud, Lebre, Anne-Sophie, Jennesson, Mélanie, Sattar, Shifteh, Marchal, Cécile, NordliJr, Douglas R, Lindstrom, Kristin, Striano, Pasquale, Lomax, Lysa Boissé, Kiss, Courtney, Bartolomei, Fabrice, Lepine, Anne Fabienne, Schoonjans, An-Sofie, Stouffs, Katrien, Jansen, Anna, Panagiotakaki, Eleni, Ricard-Mousnier, Brigitte, Thevenon, Julien, de Bellescize, Julitta, Catenoix, Hélène, Dorn, Thomas, Zenker, Martin, Müller-Schlüter, Karen, Brandt, Christian, Krey, Ilona, Polster, Tilman, Wolff, Markus, Balci, Meral, Rostasy, Kevin, Achaz, Guillaume, Zacher, Pia, Becher, Thomas, Cloppenborg, Thomas, Yuskaitis, Christopher J., Weckhuysen, Sarah, Poduri, Annapurna, Lemke, Johannes R., Møller, Rikke S., Baulac, Stéphanie
Julkaisussa Genet Med (2018)