Enzyme replacement therapy with alglucosidase alfa in 44 patients with late-onset glycogen storage disease type 2: 12-month results of an observational clinical trial von Strothotte, S., Strigl-Pill, N., Grunert, B., Kornblum, C., Eger, K., Wessig, C., Deschauer, M., Breunig, F., Glocker, F. X., Vielhaber, S., Brejova, A., Hilz, M., Reiners, K., Müller-Felber, W., Mengel, E., Spranger, M., Schoser, Benedikt

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Contrast-enhancement in the wall of a cerebral fusiform aneurysm in neuroborreliosis at 7 T MRI von Perosa, V., Bartels, C., Godenschweger, F., Speck, O., Heinze, H.J., Vielhaber, S., Schreiber, S.

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P316 Influence of transcranial direct current stimulation on electrophysiological and behavioral correlates of cognitive fatigue in multiple sclerosis von Fiene, M, Heinze, H.-J, Vielhaber, S, Zaehle, T

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Knockout of cyclophilin D in Ppif−/− mice increases stability of brain mitochondria against Ca2+ stress von Gainutdinov, T., Molkentin, J.D., Siemen, D., Ziemer, M., Debska-Vielhaber, G., Vielhaber, S., Gizatullina, Z., Orynbayeva, Z., Gellerich, F.N.

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Dyspnea in amyotrophic lateral sclerosis: The Dyspnea-ALS-Scale (DALS-15) essentially contributes to the diagnosis of respiratory impairment von Vogt, S., Schreiber, S., Kollewe, K., Körner, S., Heinze, H.-J., Dengler, R., Petri, S., Vielhaber, S.

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An integrative correlation of myopathology, phenotype and genotype in late onset Pompe disease von Kulessa, M., Weyer‐Menkhoff, I., Viergutz, L., Kornblum, C., Claeys, K. G., Schneider, I., Plöckinger, U., Young, P., Boentert, M., Vielhaber, S., Mawrin, C., Bergmann, M., Weis, J., Ziagaki, A., Stenzel, W., Deschauer, M., Nolte, D., Hahn, A., Schoser, B., Schänzer, A.

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Dysregulation of iron protein expression in the G93A model of amyotrophic lateral sclerosis von Hadzhieva, M, Kirches, E, Wilisch-Neumann, A, Pachow, D, Wallesch, M, Schoenfeld, P, Paege, I, Vielhaber, S, Petri, S, Keilhoff, G, Mawrin, C

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Modelling and shielding analysis of the neutral beam injector ports in ITER von Pereslavtsev, P., Fischer, U., Loughlin, M., Lu, Lei, Polunovskiy, E., Vielhaber, S.

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V14. Complementary use of central and peripheral non-invasive imaging to distinguish between subtypes in amyotrophic lateral sclerosis von Abdulla, S, Löwe, K, Schreiber, S, Kaufmann, J, Debska-Vielhaber, G, Machts, J, Dannhardt-Stieger, V, Petri, S, Kollewe, K, Schreiber, F, Heinze, H.-J, Dengler, R, Schoenfeld, A.M, Nestor, P.J, Vielhaber, S

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P23. Basal ganglia pathology in amyotrophic lateral sclerosis is associated with cognitive and behavioural changes von Machts, J, Loewe, K, Kaufmann, J, Jakubiczka, S, Abdulla, S, Petri, S, Dengler, R, Heinze, H.-J, Schoenfeld, M.A, Vielhaber, S, Bede, P

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Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis von Vielhaber, Stefan, Kunz, Dagmar, Winkler, Kirstin, Wiedemann, Falk R., Kirches, Elmar, Feistner, Helmut, Heinze, Hans-Jochen, Elger, Christian E., Schubert, Walter, Kunz, Wolfram S.

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Subtle cognitive dysfunction in adult onset myotonic dystrophy type 1 (DM1) and type 2 (DM2) von GAUL, C, SCHMIDT, T, WINDISCH, G, WIESER, T, MÜLLER, T, VIELHABER, S, ZIERZ, S, LEPLOW, B

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Functional motor compensation in amyotrophic lateral sclerosis von SCHOENFELD, Mircea Ariel, TEMPELMANN, C, GAUL, C, KÜHNEL, G. R, DUZEL, E, HOPF, J.-M, FEISTNER, H, ZIERZ, S, HEINZE, H.-J, VIELHABER, S

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Should a percutaneous dilational tracheostomy be guided with a bronchoscope? von Abdulla, S, Conrad, A, Vielhaber, S, Eckhardt, R, Abdulla, W

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In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient von NIESSEN, Heiko G, ANGENSTEIN, Frank, SANDER, Kerstin, KUNZ, Wolfram S, TEUCHERT, Marko, LUDOLPH, Albert C, HEINZE, Hans-Jochen, SCHEICH, Henning, VIELHABER, Stefan

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Bilateral idiopathic hypertrophy of the first dorsal interosseous muscles in a 43-year-old man von Boelmans, K, Fischbach, F, Mirastschijski, U, Vielhaber, S

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Cardiac involvement in limb-girdle muscular dystrophy 2I : conventional cardiac diagnostic and cardiovascular magnetic resonance von Gaul, C, Deschauer, M, Tempelmann, C, Vielhaber, S, Klein, H U, Heinze, H J, Zierz, S, Grothues, F

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Familial ALS in Germany: origin of the R115G SOD1 mutation by a founder effect von Niemann, S, Joos, H, Meyer, T, Vielhaber, S, Reuner, U, Gleichmann, M, Dengler, R, Müller, U

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P 44. Structural and functional brain alterations in patients with myasthenia gravis von Klaus, B., Müller, P., van Wickeren, N., Dordevic, M., Schmicker, M., Vielhaber, S., Schreiber, S., Müller, N.G.

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P 25 CSF biomarkers in CAA compared to AD von Pfister, M., Frantsev, R., Schreiber, F., Garz, C., Perosa, V., Assmann, A., Düzel, E., Butryn, M., Glanz, W., Vielhaber, S., Schreiber, S., John, A.C.

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