A primary production deficit in the thrombocytopenia of equine infectious anemia von Crawford, T.B. (Washington State University, Pullman, WA.), Wardrop, K.J, Tornquist, S.J, Reilich, E, Meyers, K.M, McGuire, T.C

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A Morphometric Study of Bone Marrow Megakaryocytes in Foals Infected with Equine Infectious Anemia Virus von Wardrop, K. J., Baszler, T. V., Reilich, E., Crawford, T. B.

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Rotary vane type pump von REILICH GUSTAVE E

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Biallelic, Selectable, Knock-in Targeting of CCR5 via CRISPR-Cas9 Mediated Homology Directed Repair Inhibits HIV-1 Replication von Scheller, Stefan H, Rashad, Yasmine, Saleh, Fayez M, Willingham, Kurtis A, Reilich, Antonia, Lin, Dong, Izadpanah, Reza, Alt, Eckhard U, Braun, Stephen E

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G.P.166 von Schreiber, O, Klug, C, Thiele, S, Schorling, E, Zowe, J, Reilich, P, Nagels, K, Walter, M.C

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G.P.166: Comparative economic impact of therapeutic innovation on health care burden of Duchenne Muscular Dystrophy (DMD) using Becker Muscular Dystrophy (BMD) as a comparator for... von Schreiber, O., Klug, C., Thiele, S., Schorling, E., Zowe, J., Reilich, P., Nagels, K., Walter, M.C.

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Muscle pathology in 57 patients with myotonic dystrophy type 2 von Schoser, Benedikt G.H., Schneider-Gold, Christiane, Kress, Wolfram, Goebel, Hans-Hilmar, Reilich, Peter, Koch, Manuela C., Pongratz, Dieter E., Toyka, Klaus V., Lochmüller, Hanns, Ricker, Kenneth

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P64 Neutral lipid storage myopathy due to PNPLA2 mutations may respond to beta-adrenergic treatment von Horvath, R, Reilich, P, Krause, S, Turnbull, D.M, Trenell, M, Hollingsworth, K.G, Gorman, G.S, Czermin, B, Holinski-Feder, E, Walter, M.C, Schoser, B, Lochmüller, H

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Creatine monohydrate in myotonic dystrophy: A double-blind, placebo-controlled clinical study von WALTER, Maggie C, REILICH, Peter, LOCHMÜLLER, Hanns, KOHNEN, Ralph, SCHLOTTER, Beate, HAUTMANN, Hubert, DUNKL, Elmar, PONGRATZ, Dieter, MÜLLER-FELBER, Wolfgang

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FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients von Walter, M C, Petersen, J A, Stucka, R, Fischer, D, Schröder, R, Vorgerd, M, Schroers, A, Schreiber, H, Hanemann, C O, Knirsch, U, Rosenbohm, A, Huebner, A, Barisic, N, Horvath, R, Komoly, S, Reilich, P, Müller-Felber, W, Pongratz, D, Müller, J S, Auerswald, E A, Lochmüller, H

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FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients von Walter, M C, Petersen, J A, Stucka, R, Fischer, D, Schröder, R, Vorgerd, M, Schroers, A, Schreiber, H, Hanemann, C O, Knirsch, U, Rosenbohm, A, Huebner, A, Barisic, N, Horvath, R, Komoly, S, Reilich, P, Muller-Felber, W, Pongratz, D, Muller, J S, Auerswald, E A, Lochmuller, H

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Identification of a desmin gene mutation in scapuloperoneal syndrome von Walter, MC, Reilich, P, Huebner, A, Fischer, D, Vorgerd, M, Born, C, Schoser, BG, Klutzny, U, Frey, J, Kaeser, HE, Lochmüller, H

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Identification of a desmin gene mutation in scapuloperoneal syndrome von Walter, MC, Reilich, P, Huebner, A, Fischer, D, Vorgerd, M, Born, C, Schoser, BG, Klutzny, U, Frey, J, Kaeser, HE, Lochmüller, H

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Quantitative determination of cyclopropenoid fatty acids in cottonseed meal von Levi, R. S., Reilich, H. G., O舗Neill, H. J., Cucullu, Alva F., Skau, E. L.

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