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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Springe zu: 2017
Anzahl der Publikationen: 6
2017
Krause, S.; Reichert, S.; Donandt, T.; Kalbe, C.; Schmuck, M.; Klymiuk, N.; Kessler, B.; Blutke, A.; Wolf, E.; Schoser, B. und Walter, M.
(2017):
Molecular therapy in a novel translational large animal model for Duchenne muscular dystrophy.
In: Neuromuscular Disorders, Bd. 27:
S188-S189
Walter, M.; Reilich, P.; Krause, S.; Abicht, A. und Schoser, B.
(2017):
Congenital centronuclear myopathy and epidermolysis bullosa due to two novel mutations in the plectin gene.
In: Neuromuscular Disorders, Bd. 27:
S112-S112
James, M.; Jacobs, M.; Mayhew, A.; Feng, J.; Spuler, S.; Day, J.; Jones, K.; Bharucha-Göbel, D.; Salort-Campana, E.; Pestronk, A.; Walter, M.; Paradas, C.; Stojkovic, T.; Mori-Yoshimura, M.; Bravver, E.; Diaz-Manera, J.; Pegoraro, E.; Mendell, J.; Bushby, K. und Straub, V.
(2017):
Clinical outcome study of dysferlinopathy: what are the best outcome measures for dysferlinopathy patients?
In: Neuromuscular Disorders, Bd. 27:
S227-S227
Palmio, J.; Leonard, S.; Sacconi, S.; Savarese, M.; Semmler, A.; Bach, J.; Kress, W.; Mozaffar, T.; Lai, T.; Stojkovic, T.; Schoser, B.; Walter, M.; Reisin, R.; Berardo, A.; Attarian, S.; Urtizberea, A.; Fatehi, F.; Hackman, P. und Udd, B.
(2017):
Expanding importance of HMERF titinopathy: new mutations and clinical aspects.
In: Neuromuscular Disorders, Bd. 27:
S237-S237
Torron, R. Fernandez; Harris, E.; Bourke, J.; Bettinson, K.; Hilsden, H.; Spuler, S.; Day, J.; Jones, K.; Bharucha-Göbel, D.; Salort-Campana, E.; Pestronk, A.; Walter, M.; Paradas, C.; Stojkovic, T.; Mori-Yoshimura, M.; Bravver, E.; Diaz-Manera, J.; Pegoraro, E.; Mendell, J.; Bushby, K. und Straub, V.
(2017):
Is cardiac dysfunction a feature of dysferlinopathy? Data from the clinical outcome study of dysferlinopathy.
In: Neuromuscular Disorders, Bd. 27:
S145-S145
Schiffer, B.; Amelung, T.; Pohl, A.; Kärgel, C.; Tenbergen, G.; Gerwinn, H.; Mohnke, S.; Massau, C.; Matthias, W.; Weiss, S.; Marr, V.; Beier, K. M.; Walter, M.; Ponseti, J.; Krüger, T. H. C.; Schiltz, K. und Walter, H.
(2017):
Gray matter anomalies in pedophiles with and without a history of child sexual offending.
In: Translational Psychiatry, Bd. 7, e1129