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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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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Relationship of substance P, 5-hydroxyindole acetic acid and tryptophan in serum of fibromyalgia patients von Schwarz, Marcus J, Späth, Michael, Müller-Bardorff, Hanns, Pongratz, Dieter E, Bondy, Brigitta, Ackenheil, Manfred

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The T102C Polymorphism of the 5-HT2A-Receptor Gene in Fibromyalgia von Bondy, Brigitta, Spaeth, Michael, Offenbaecher, Martin, Glatzeder, Karin, Stratz, Thomas, Schwarz, Markus, de Jonge, Sylvia, Krüger, Marc, Engel, Rolf R., Färber, Lothar, Pongratz, Dieter E., Ackenheil, Manfred

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Detection of elevated Nε-carboxymethyllysine levels in muscular tissue and in serum of patients with fibromyalgia von Rüster, M., Franke, S., Späth, M., Pongratz, D. E., Stein, G., Hein, G. E.

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Breaking the news in amyotrophic lateral sclerosis von Borasio, Gian Domenico, Sloan, Richard, Pongratz, Dieter E

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Magnetic resonance imaging of skeletal muscles in idiopathic inflammatory myopathies of adults von REIMERS, C. D, SCHEDEL, H, FLECKENSTEIN, J. L, NÄGELE, M, WITT, T. N, PONGRATZ, D. E, WOGL, T. J

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Muscular ultrasound in idiopathic inflammatory myopathies of adults von Reimers, Carl D., Fleckenstein, James L., Witt, Thomas N., Müller-Felber, Wolfgang, Pongratz, Dieter E.

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Altered pattern of insulin receptor isotypes in skeletal muscle membranes of type 2 (non-insulin-dependent) diabetic subjects von KELLERER, M, SESTI, G, SEFFER, E, OBERMAIER-KUSSER, B, PONGRATZ, D. E, MOSTHAF, L, HÄRING, H. U

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A defective Intramolecular Autoactivation Cascade May Cause the Reduced Kinase Activity of the Skeletal Muscle Insulin Receptor from Patients with Non-insulin-dependent Diabetes Me... von Obermaier-Kusser, B, White, M F, Pongratz, D E, Su, Z, Ermel, B, Muhlbacher, C, Haring, H U

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Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis von Müller-Felber, W, Ansevin, C.F, Ricker, K, Müller-Jenssen, A, Töpfer, M, Goebel, H.H, Pongratz, D.E

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Imaging techniques in myotonic dystrophy. A comparative study of ultrasound, computed tomography and magnetic resonance imaging of skeletal muscles von Schedel, H., Reimers, C.D., Nägele, M., Witt, Th.N., Pongratz, D.E., Vogl, Th

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Marinesco Sjögren Syndrome with Rhabdomyolysis. A New Subtype of the Disease von Müller-Felber, W., Zafiriou, D., Scheck, R., Pätzke, I., Toepfer, M., Pongratz, D. E., Walther, U.

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Morphologic aspects of fibromyalgia von Pongratz, D E, Späth, M

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Discrepant results for cardiac troponin T and troponin I in chronic myopathy, depending on instrument and assay generation von BRAUN, S. L, PONGRATZ, D. E, BIALK, P, LIEM, S, SCHLOTTER, B, VOGT, W

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Immunohistological analysis of sarcoid myopathy von Tews, D S, Pongratz, D E

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Mutational analysis of serotonin receptor genes: HTR3A and HTR3B in fibromyalgia patients von Frank, Bernd, Niesler, Beate, Bondy, Brigitta, Späth, Michael, Pongratz, Dieter E, Ackenheil, Manfred, Fischer, Christine, Rappold, Gudrun

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A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgro... von Jaksch, M, Hofmann, S, Kleinle, S, Liechti-Gallati, S, Pongratz, D E, Müller-Höcker, J, Jedele, K B, Meitinger, T, Gerbitz, K D

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Upregulation of utrophin in the myocardium of a carrier of Duchenne muscular dystrophy von BEHR, T. M., FISCHER, P., MUDRA, H., THEISEN, K., SPES, C., ÜBERFUHR, P., MÜLLER-FELBER, W., PONGRATZ, D. E., ANGERMANN, C.

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Fibromyalgia - symptom or diagnosis: A definition of the position von Sievers, Dieter Pongratz, Marcus

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