 | Up a level |
2018
Schara, U., Fink, G. R. and von Moers, A. (2018). Transition from neuropediatrics to neurology in neuromuscular diseases. Nervenarzt, 89 (10). S. 1123 - 1131. NEW YORK: SPRINGER. ISSN 1433-0407
2017
Wang, H., Salter, S., Refai, O., Hardy, H., Sejersen, T., Wright, J., Zimmerman, H., Weis, J., Schara, U., Russell, M., Abdul-Rahman, O., Chilton, J., Blakely, R., Baple, E., Crosby, A. and Cirak, S. (2017). Recessively-acting choline transporter mutations associated with severe congenital myasthenia disrupt transporter surface trafficking in vitro and in vivo. Neuromusc. Disord., 27. S. S220 - 2. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364
2012
Trippe, H., Munteanu, M., Stehling, F., Mellies, U., Vincent, A., Schneider-Gold, C., Heller, R. and Schara, U. (2012). Myasthenic symptoms: From initial presentation to diagnosis. Neuromusc. Disord., 22 (9-10). S. 856 - 857. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0960-8966