Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited von Schoser, B. G. H., Müller-Höcker, J., Horvath, R., Gempel, K., Pongratz, D., Lochmüller, H., Müller-Felber, W.

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Serum Levels of Matrix Metalloproteinases-2 and -9 and Their Tissue Inhibitors in Inflammatory Neuromuscular Disorders von Hurnaus, S., Mueller-Felber, W., Pongratz, D., Schoser, B.G.H.

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Coenzyme Q10 deficiency and isolated myopathy von HORVATH, R, SCHNEIDERAT, P, LOCHMÜLLER, H, SCHOSER, B. G. H, GEMPEL, K, NEUEN-JACOB, E, PLÖGER, H, MÜLLER-HÖCKER, J, PONGRATZ, D. E, NAINI, A, DIMAURO, S

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Molecular biomarkers monitoring human skeletal muscle fibres and microvasculature following long‐term bed rest with and without countermeasures von Salanova, M., Schiffl, G., Püttmann, B., Schoser, B. G., Blottner, D.

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Matrix metalloproteinases MMP-2, MMP-7 and MMP-9 in denervated human muscle von Schoser, Benedikt G. H, Blottner, D

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Matrix metalloproteinases in inflammatory myopathies: enhanced immunoreactivity near atrophic myofibers von Schoser, B. G. H., Blottner, D., Stuerenburg, H.-J.

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Sudden cardiac death in myotonic dystrophy type 2 von SCHOSER, B. G. H, RICKER, K, SCHNEIDER-GOLD, C, HENGSTENBERG, C, DÜRRE, J, BÜLTMANN, B, KRESS, W, DAY, J. W, RANUM, L. P. W

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Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P von Walter, M. C., Reilich, P., Huebner, A., Fischer, D., Schröder, R., Vorgerd, M., Kress, W., Born, C., Schoser, B. G., Krause, K. H., Klutzny, U., Bulst, S., Frey, J. R., Lochmüller, H.

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Outcome and effect of pregnancy in myotonic dystrophy type 2 von RUDNIK-SCHÖNEBORN, S, SCHNEIDER-GOLD, C, RAABE, U, KRESS, W, ZERRES, K, SCHOSER, B. G. H

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McLeod myopathy revisited: more neurogenic and less benign von Hewer, Ekkehard, Danek, Adrian, Schoser, Benedikt G., Miranda, Marcelo, Reichard, Ross, Castiglioni, Claudia, Oechsner, Matthias, Goebel, Hans H., Heppner, Frank L., Jung, Hans H.

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Autoimmune hyperthyroidism in multiple sclerosis under treatment with glatiramer acetate - a case report von Heesen, C., Gbadamosi, J., Schoser, B.-G.-H., Pöhlau, D.

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Spontaneous recovery of a childhood onset mitochondrial myopathy caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene von Horváth, R, Lochmüller, H, Hoeltzenbein, M, Müller-Höcker, J, Schoser, B G, Pongratz, D, Jaksch, M

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A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation von VORGERD, M, RICKER, K, ZIEMSSEN, F, KRESS, W, GOEBEL, H. H, NIX, W. A, KUBISCH, C, SCHOSER, B. G. H, MORTIER, W

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Mutations in the acid α-glucosidase gene (M. Pompe) in a patient with an unusual phenotype von ANNESER, J. M. H, PONGRATZ, D. E, PODSKARBI, T, SHIN, Y. S, SCHOSER, B. G. H

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Cerebral hyperperfusion injury after percutaneous transluminal angioplasty of extracranial arteries von SCHOSER, B. G. H, HEESEN, C, ECKERT, B, THIE, A

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A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy von Horváth, R, Lochmüller, H, Scharfe, C, Do, B H, Oefner, P J, Müller-Höcker, J, Schoser, B G, Pongratz, D, Auer, D P, Jaksch, M

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CD95-mediated apoptosis and DNA fragmentation in MS von Heesen, C., Georghiu, S., Gbadamosi, J., Schoser, B. G. H.

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Pathological consequences of VCP mutations on human striated muscle von Hübbers, Christian U., Clemen, Christoph S., Kesper, Kristina, Böddrich, Annett, Hofmann, Andreas, Kämäräinen, Outi, Tolksdorf, Karen, Stumpf, Maria, Reichelt, Julia, Roth, Udo, Krause, Sabine, Watts, Giles, Kimonis, Virginia, Wattjes, Mike P., Reimann, Jens, Thal, Dietmar R., Biermann, Katharina, Evert, Bernd O., Lochmüller, Hanns, Wanker, Erich E., Schoser, Benedikt G. H., Noegel, Angelika A., Schröder, Rolf

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Novel missense mutation in the caveolin-3 gene in a Belgian family with rippling muscle disease von Van den Bergh, P Y K, Gérard, J M, Elosegi, J A, Manto, M U, Kubisch, C, Schoser, B G H

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Subacute onset of oculogyric crises and generalized dystonia following intranasal administration of heroin von Schoser, Benedikt G.H., Groden, Christoph

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