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Muscle & nerve, 2024-08, Vol.70 (2), p.257-264
2024
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European journal of neurology, 2021-08, Vol.28 (8), p.2582-2595
- Meyer, Thomas
- Maier, André
- Uzelac, Zeljko
- Hagenacker, Tim
- Günther, René
- Schreiber‐Katz, Olivia
- Weiler, Markus
- Steinbach, Robert
- Weyen, Ute
- Koch, Jan Christoph
- Kettemann, Dagmar
- Norden, Jenny
- Dorst, Johannes
- Wurster, Claudia
- Ludolph, Albert C.
- Stolte, Benjamin
- Freigang, Maren
- Osmanovic, Alma
- Petri, Susanne
- Grosskreutz, Julian
- Rödiger, Annekathrin
- Griep, Ramona
- Gaudlitz, Marcel
- Walter, Bertram
- Münch, Christoph
- Spittel, Susanne
2021
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PLoS genetics, 2015-11, Vol.11 (11), p.e1005655-e1005655
2015
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The Journal of pediatrics, 2022-07, Vol.246, p.251-265.e2
2022
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The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations
- Bladen, Catherine L.
- Salgado, David
- Monges, Soledad
- Foncuberta, Maria E.
- Kekou, Kyriaki
- Kosma, Konstantina
- Dawkins, Hugh
- Lamont, Leanne
- Roy, Anna J.
- Chamova, Teodora
- Guergueltcheva, Velina
- Chan, Sophelia
- Korngut, Lawrence
- Campbell, Craig
- Dai, Yi
- Wang, Jen
- Barišić, Nina
- Brabec, Petr
- Lahdetie, Jaana
- Walter, Maggie C.
- Schreiber-Katz, Olivia
- Karcagi, Veronika
- Garami, Marta
- Viswanathan, Venkatarman
- Bayat, Farhad
- Buccella, Filippo
- Kimura, En
- Koeks, Zaïda
- van den Bergen, Janneke C.
- Rodrigues, Miriam
- Roxburgh, Richard
- Lusakowska, Anna
- Kostera-Pruszczyk, Anna
- Zimowski, Janusz
- Santos, Rosário
- Neagu, Elena
- Artemieva, Svetlana
- Rasic, Vedrana Milic
- Vojinovic, Dina
- Posada, Manuel
- Bloetzer, Clemens
- Jeannet, Pierre-Yves
- Joncourt, Franziska
- Díaz-Manera, Jordi
- Gallardo, Eduard
- Karaduman, A. Ayşe
- Topaloğlu, Haluk
- El Sherif, Rasha
- Stringer, Angela
- Shatillo, Andriy V.
- Martin, Ann S.
- Peay, Holly L.
- Bellgard, Matthew I.
- Kirschner, Jan
- Flanigan, Kevin M.
- Straub, Volker
- Bushby, Kate
- Verschuuren, Jan
- Aartsma-Rus, Annemieke
- Béroud, Christophe
- Lochmüller, Hanns
2015
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Annals of clinical and translational neurology, 2021-05, Vol.8 (5), p.1049-1063
- Freigang, Maren
- Wurster, Claudia D.
- Hagenacker, Tim
- Stolte, Benjamin
- Weiler, Markus
- Kamm, Christoph
- Schreiber‐Katz, Olivia
- Osmanovic, Alma
- Petri, Susanne
- Kowski, Alexander
- Meyer, Thomas
- Koch, Jan C.
- Cordts, Isabell
- Deschauer, Marcus
- Lingor, Paul
- Aust, Elisa
- Petzold, Daniel
- Ludolph, Albert C.
- Falkenburger, Björn
- Hermann, Andreas
- Günther, René
2021
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BMC neurology, 2024-02, Vol.24 (1), p.67-67, Article 67
2024
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Orphanet journal of rare diseases, 2020-06, Vol.15 (1), p.1-149, Article 149
2020
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Scientific reports, 2023-04, Vol.13 (1), p.6240-6240, Article 6240
2023
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Annals of clinical and translational neurology, 2022-09, Vol.9 (9), p.1437-1448
2022
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Brain sciences, 2021-02, Vol.11 (3), p.296
2021
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American journal of medical genetics. Part C, Seminars in medical genetics, 2016-06, Vol.172C (2), p.92-101
2016
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Validity and reliability of the German multidimensional fatigue inventory in spinal muscular atrophy
- Binz, Camilla
- Osmanovic, Alma
- Thomas, Nele H.
- Stolte, Benjamin
- Freigang, Maren
- Cordts, Isabell
- Griep, Ramona
- Uzelac, Zeljko
- Wurster, Claudia D.
- Kamm, Christoph
- Siegler, Hannah A.
- Wieselmann, Gary
- Hermann, Andreas
- Lingor, Paul
- Deschauer, Marcus
- Ludolph, Albert C.
- Meyer, Thomas
- Günther, René
- Hagenacker, Tim
- Petri, Susanne
- Schreiber‐Katz, Olivia
2022
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Annals of clinical and translational neurology, 2020-05, Vol.7 (5), p.757-766
2020
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Orphanet journal of rare diseases, 2021-07, Vol.16 (1), p.330-330, Article 330
2021
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Orphanet journal of rare diseases, 2021-01, Vol.16 (1), p.10-10, Article 10
2021
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Brain sciences, 2021-03, Vol.11 (3), p.367
2021
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Journal of neuromuscular diseases, 2017-11, Vol.4 (4), p.293-306
- Koeks, Zaïda
- Bladen, Catherine L
- Salgado, David
- van Zwet, Erik
- Pogoryelova, Oksana
- McMacken, Grace
- Monges, Soledad
- Foncuberta, Maria E
- Kekou, Kyriaki
- Kosma, Konstantina
- Dawkins, Hugh
- Lamont, Leanne
- Bellgard, Matthew I
- Roy, Anna J
- Chamova, Teodora
- Guergueltcheva, Velina
- Chan, Sophelia
- Korngut, Lawrence
- Campbell, Craig
- Dai, Yi
- Wang, Jen
- Barišić, Nina
- Brabec, Petr
- Lähdetie, Jaana
- Walter, Maggie C
- Schreiber-Katz, Olivia
- Karcagi, Veronika
- Garami, Marta
- Herczegfalvi, Agnes
- Viswanathan, Venkatarman
- Bayat, Farhad
- Buccella, Filippo
- Ferlini, Alessandra
- Kimura, En
- van den Bergen, Janneke C
- Rodrigues, Miriam
- Roxburgh, Richard
- Lusakowska, Anna
- Kostera-Pruszczyk, Anna
- Santos, Rosário
- Neagu, Elena
- Artemieva, Svetlana
- Rasic, Vedrana Milic
- Vojinovic, Dina
- Posada, Manuel
- Bloetzer, Clemens
- Klein, Andrea
- Díaz-Manera, Jordi
- Gallardo, Eduard
- Karaduman, A Ayşe
- Oznur, Tunca
- Topaloğlu, Haluk
- El Sherif, Rasha
- Stringer, Angela
- Shatillo, Andriy V
- Martin, Ann S
- Peay, Holly L
- Kirschner, Jan
- Flanigan, Kevin M
- Straub, Volker
- Bushby, Kate
- Béroud, Christophe
- Verschuuren, Jan J
- Lochmüller, Hanns
2017
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Experimental neurology, 2015-09, Vol.271, p.189-197
2015
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American journal of medical genetics. Part A, 2019-06, Vol.179 (6), p.1080-1090
- Kline, Antonie D.
- Krantz, Ian D.
- Bando, Masashige
- Shirahige, Katsuhiko
- Chea, Stephenson
- Sakata, Toyonori
- Rao, Suhas
- Dorsett, Dale
- Singh, Vijay Pratap
- Gerton, Jennifer L.
- Horsfield, Julia A.
- Calof, Anne L.
- Katz, Olivia
- Grados, Marco
- Raible, Sarah
- Barañano, Kristin
- Lyon, Gholson
- Musio, Antonio
- Carrico, Cheri S.
- Clemens, Douglas K.
- Caudill, Patti
- Massa, Valentina
- McGill, Bryan E.
- Dommestrup, Aila
- O'Connor, Julia
- Haaland, Richard E.
2019
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Orphanet journal of rare diseases, 2014-12, Vol.9 (1), p.210-210, Article 210
2014
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American journal of medical genetics. Part A, 2017-05, Vol.173 (5), p.1172-1185
- Kline, Antonie D.
- Krantz, Ian D.
- Deardorff, Matthew A.
- Shirahige, Katsuhiko
- Dorsett, Dale
- Gerton, Jennifer L.
- Wu, Meng
- Mehta, Devanshi
- Mills, Jason A.
- Carrico, Cheri S.
- Noon, Sarah
- Herrera, Pamela S.
- Horsfield, Julia A.
- Bettale, Chiara
- Morgan, Jeremy
- Huisman, Sylvia A.
- Moss, Jo
- McCleery, Joseph
- Grados, Marco
- Hansen, Blake D.
- Srivastava, Siddharth
- Taylor‐Snell, Emily
- Kerr, Lynne M.
- Katz, Olivia
- Calof, Anne L.
- Musio, Antonio
- Egense, Alena
- Haaland, Richard E.
2017
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Therapeutic advances in neurological disorders, 2021, Vol.14, p.1756286421998902-1756286421998902
2021
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Brain sciences, 2021-06, Vol.11 (6), p.748
- Schischlevskij, Pavel
- Cordts, Isabell
- Günther, René
- Stolte, Benjamin
- Zeller, Daniel
- Schröter, Carsten
- Weyen, Ute
- Regensburger, Martin
- Wolf, Joachim
- Schneider, Ilka
- Hermann, Andreas
- Metelmann, Moritz
- Kohl, Zacharias
- Linker, Ralf A.
- Koch, Jan Christoph
- Stendel, Claudia
- Müschen, Lars H.
- Osmanovic, Alma
- Binz, Camilla
- Klopstock, Thomas
- Dorst, Johannes
- Ludolph, Albert C.
- Boentert, Matthias
- Hagenacker, Tim
- Deschauer, Marcus
- Lingor, Paul
- Petri, Susanne
- Schreiber-Katz, Olivia
2021
Volltextzugriff (PDF)
Genes, 2022-01, Vol.13 (1), p.84
2022
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