 | Up a level |
2014
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
2013
Rachwalski, M., Wollnik, B. and Kress, W. (2013). Clinical course and genetics of syndromic and non-syndromic craniosynostosis. Med. Genet., 25 (3). S. 373 - 386. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1863-5490
2011
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