Physiological Evaluation of Solvent‐Treated Cottonseed Meals in Rations for Laying Hens von Proctor, J., O’Neill, H. J., Reilich, H. G., Levi, R. S., Pons, W. A.

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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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Classification of corn odor by statistical analysis of gas chromatographic patterns of headspace volatiles von Dravnieks, A, Reilich, H.G, Whitfield, J, Watson, C.A

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Development of a phosphate‐free home laundry detergent von Linfield, W. M., Roseman, K. A., Reilich, H. G., Adlaf, P. C., Harlin, C. C.

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Chemical inactivation of cyclopropenoid fatty acids in cottonseed meals and their physiological evaluation von Reilich, H. G., O'neill, H. J., Levi, R. S., Proctor, J., Pons, W. A.

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Removal of cyclopropenoid fatty acids from cottonseed meals by solvent extraction von Reilich, H. G., O’Neill, H. J., Levi, R. S., Yamauchi, T., Pons, W. A.

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The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene von Reilich, Peter, Horvath, Rita, Krause, Sabine, Schramm, Nicolai, Turnbull, Doug M., Trenell, Michael, Hollingsworth, Kieren G., Gorman, Grainne S., Hans, Volkmar H., Reimann, Jens, MacMillan, Andrée, Turner, Lesley, Schollen, Annette, Witte, Gregor, Czermin, Birgit, Holinski-Feder, Elke, Walter, Maggie C., Schoser, Benedikt, Lochmüller, Hanns

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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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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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Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery–Dreifuss muscular dystrophy von Walter, Maggie C., Witt, Thomas N., Weigel, Beate Schlotter, Reilich, Peter, Richard, Pascale, Pongratz, Dieter, Bonne, Gisèle, Wehnert, Manfred S., Lochmüller, Hanns

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Accuracy of botulinum toxin injections in myofascial pain. Response to Gobel et al. Pain 2006;125:82–8 von Reilich, Peter, Schoser, Benedikt G.H.

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De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy von Durling, H.J, Reilich, P, Müller-Höcker, J, Mendel, B, Pongratz, D, Wallgren-Pettersson, C, Gunning, P, Lochmüller, H, Laing, N.G

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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. Commentary von WALTER, M. C, REILICH, P, KLUTZNY, U, BULST, S, FREY, J. R, LOCHMÜLLER, H, LAING, Nigel G, BLOCK, B, HUEBNER, A, FISCHER, D, SCHRÖDER, R, VORGERD, M, KRESS, W, BORN, C, SCHOSER, B. G, KRAUSE, K. H

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Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy von Müller, Juliane S., Piko, Henriett, Schoser, Benedikt G.H., Schlotter-Weigel, Beate, Reilich, Peter, Gürster, Stefanie, Born, Christine, Karcagi, Veronika, Pongratz, Dieter, Lochmüller, Hanns, Walter, Maggie C.

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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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