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Jump to: 2017
Number of items: 2.

2017

Malfatti, E.; Goillot, E.; Streichenberger, N.; Leonard-Louis, S.; Brochier, G.; Madelaine, A.; Labasse, C.; Nadaj-Pakleza, A.; Sacconi, S.; Schoser, B.; Oldfors, A.; Eymard, B.; Romero, N.; Vissing, J. und Laforet, P. (2017): Autophagy impairment in muscle biopsies from debranching enzyme deficiency (GSDIII) patients: pinpointing novel therapeutic perspectives. In: Neuromuscular Disorders, Vol. 27: S205-S206

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, Vol. 27: S237-S237

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