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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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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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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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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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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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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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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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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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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Homozygosity for CCTG mutation in myotonic dystrophy type 2 von Schoser, Benedikt G. H., Kress, Wolfram, Walter, Maggie C., Halliger-Keller, Birgit, Lochmüller, Hanns, Ricker, Kenneth

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

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

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Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy von Horváth, R., Schoser, B.G.H., Müller-Höcker, J., Völpel, M., Jaksch, M., Lochmüller, H.

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Prediction of response to IVIg treatment in patients with lower motor neurone disorders von Strigl-Pill, N., König, A., Schröder, M., Beranek, H., Schoser, B.G.H., Spaeth, M., Pongratz, D., Müller-Felber, W.

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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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Immunolocalization of leukemia inhibitory factor in normal and denervated human muscle von Schoser, Benedikt G. H, Storjohann, Stefan, Kunze, Klaus

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Acute overdosage and intoxication with carbidopa/levodopa can be detected in the subacute stage by measurement of 3-o-methyldopa von STUERENBURG, H J, SCHOSER, B G H

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