Universität zu Köln

Journal Article

Feldkirchner, S., Mueller, S., Kress, W., Hanisch, F. G., Schoser, B. and Schessl, J. (2011). Evaluation of standardized protein pattern of skeletal muscle fibers via laser microdissection. Neuromusc. Disord., 21 (9-10). S. 739 - 741. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0960-8966

Feldkirchner, S., Walter, M. C., Kubny, C., Mueller, S., Kress, W., Hanisch, F. G., Schoser, B. and Schessl, J. (2011). The C224W FHL1 mutation is causing a protein aggregation disorder of muscle: Two brothers revisited. Neuromusc. Disord., 21 (9-10). S. 740 - 741. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0960-8966

Geier, S., Heber, U., Tillich, A., Hirsch, H., Edelmann, H., Schaffenroth, V., Kupfer, T., Mueller, S., Maxted, P. F. L., Ostensen, R., Podsiadlowski, P., Marsh, T., Gaensicke, B., Morales-Rueda, L., Nelemans, G., Napiwotzki, R., Guenther, E. W. and Carone, L. (2010). Hot subdwarfs in binary systems and the nature of their unseen companions. Astrophys. Space Sci., 329 (1-2). S. 91 - 100. DORDRECHT: SPRINGER. ISSN 1572-946X

Schessl, J., Bach, E., Rost, S., Feldkirchner, S., Kubny, C., Mueller, S., Hanisch, F. G., Kress, W. and Schoser, B. (2014). Novel recessive myotilin mutation cause severe myofibrillar myopathy. Neuromusc. Disord., 24 (9-10). S. 832 - 833. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364

Syrbe, S., Hedrich, U., Riesch, E., Djemie, T., Mueller, S., Moller, R. S., Maher, B., Hernandez-Hernandez, L., Synofzik, M., Caglayan, H., Arslan, M., Serratosa, J., Nothnagel, M. ORCID: 0000-0001-8305-7114, May, P., Krause, R., Loeffler, H., Detert, K., Dorn, T., Vogt, H., Kraemer, G., Schoels, L., Mullis, P., Linnankivi, T., Lehesjoki, A. -E., Sterbova, K., Craiu, D., Hoffman-Zacharska, D., Korff, C., Weber, Y., Steinlin, M., Gallati, S., Bertsche, A., Bernhard, M., Merkenschlager, A., Kiess, W., Gonzalez, M., Zuechner, S., Palotie, A., Suls, A., De Jonghe, P., Helbig, I., Biskup, S., Wolff, M., Maljevic, S., Schuele, R., Sisodiya, S., Weckhuysen, S., Lerche, H. and Lemke, J. (2015). DE NOVO LOSS- OR GAIN-OF-FUNCTION MUTATIONS IN KCNA2 CAUSE EPILEPTIC ENCEPHALOPATHY. Epilepsia, 56. S. 77 - 78. HOBOKEN: WILEY-BLACKWELL. ISSN 1528-1167

Syrbe, S., Hedrich, U., Riesch, E., Djemie, T., Mueller, S., Moller, R. S., Maher, B., Hernandez-Hernandez, L., Synofzik, M., Caglayan, H., Arslan, M., Serratosa, J., Nothnagel, M. ORCID: 0000-0001-8305-7114, May, P., Krause, R., Loeffler, H., Detert, K., Dorn, T., Vogt, H., Kraemer, G., Schoels, L., Mullis, P., Linnankivi, T., Lehesjoki, A. -E., Sterbova, K., Craiu, D., Hoffman-Zacharska, D., Korff, C., Weber, Y., Steinlin, M., Gallati, S., Bertsche, A., Bernhard, M., Merkenschlager, A., Kiess, W., Gonzalez, M., Zuechner, S., Palotie, A., Suls, A., De Jonghe, P., Helbig, I., Biskup, S., Wolff, M., Maljevic, S., Schuele, R., Sisodiya, S., Weckhuysen, S., Lerche, H. and Lemke, J. (2015). DE NOVO LOSS- OR GAIN-OF-FUNCTION MUTATIONS IN KCNA2 CAUSE EPILEPTIC ENCEPHALOPATHY. Epilepsia, 56. S. 77 - 78. HOBOKEN: WILEY-BLACKWELL. ISSN 1528-1167