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Journal Article
Balke, M., Sprenger, A., Wunderlich, G., Stettner, M., Fink, G. R. and Lehmann, H. C. (2017). PREVALENCE OF PERIPHERAL NEUROPATHY AMONG FREQUENT FLYERS - IS THERE A LINK TO AEROTOXIC SYNDROME? J. Peripher. Nerv. Syst., 22 (3). S. 238 - 239. HOBOKEN: WILEY. ISSN 1529-8027
Balke, M., Wunderlich, G., Brunn, A., Fink, G. R. and Lehmann, H. C. (2016). Chronic Inflammatory Demyelinating Polyneuropathy. Forschritte Neurol. Psychiatr., 84 (12). S. 756 - 769. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-3522
Bobylev, I., Elter, T., Schneider, C., Wunderlich, G., Zimmer, P., Streckmann, F., Fink, G. R. and Lehmann, H. C. (2015). Chemotherapy-induced Peripheral Neuropathy. Forschritte Neurol. Psychiatr., 83 (8). S. 427 - 437. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-3522
Ceccon, G., Lehmann, H. C., Neuen-Jacob, E., Meng, G., Fink, G. R. and Wunderlich, G. (2017). Therapy-resistant polymyositis - is the diagnosis correct? Z. Rheumatol., 76 (7). S. 640 - 644. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1435-1250
Ferreira, N. Mendoza, Karakaya, M., Cengiz, N., Beijer, D., Fuhrmann, N., Hoelker, I., Schrank, B., Brigatti, K., Gonzaga-Jauregui, C., Puffenberger, E., Wunderlich, G., De Jonghe, P., Deconinck, T., Strauss, K., Baets, J. and Wirth, B. (2020). Mutations in the Golgi protein GBF1 as a novel cause of distal hereditary motor neuropathy. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 99 - 100. LONDON: SPRINGERNATURE. ISSN 1476-5438
Huber, C. A., Wunderlich, G., Brunn, A., Blau, T., Fink, G. R. and Lehmann, H. C. (2015). 25-year old Patient with anginal Symptoms during the muslim Fasting Month. Dtsch. Med. Wochenschr., 140 (3). S. 202 - 206. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-4413
Karakaya, M., Keller, N., Altmueller, J., Motameny, S., Thiele, H., Wunderlich, G., Kirschner, J., Schrank, B., Maroofian, R., Paketci, C., Yis, U., Nuernberg, P. and Wirth, B. (2020). Variants causing mitochondrial dysfunction are not rare in non-5q SMA: Re-evaluation of thirty families by exome sequencing. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 442 - 443. LONDON: SPRINGERNATURE. ISSN 1476-5438
Rabenstein, M., Weis, J., Abicht, A., Fink, G. R., Lehmann, H. C. and Wunderlich, G. (2020). Multiple acyl-CoA dehydrogenase deficiency/glutaric aciduria type 2: difficult diagnosis, easy to treat. Nervenarzt, 91 (4). S. 349 - 353. NEW YORK: SPRINGER. ISSN 1433-0407
Ritter, C., Wunderlich, G., Macht, S., Schroeter, M., Fink, G. R. and Lehmann, H. C. (2014). Differential diagnostics of diseases of the brachial plexus. Nervenarzt, 85 (2). S. 176 - 188. NEW YORK: SPRINGER. ISSN 1433-0407
Wunderlich, G., Abicht, A., Brunn, A., Daimagueler, H. -S., Schroeter, M., Fink, G. R., Lehmann, H. C. and Cirak, S. (2019). Congenitalmyasthenic syndromes in adulthood. Challenging, rare but treatable. Nervenarzt, 90 (2). S. 148 - 160. NEW YORK: SPRINGER. ISSN 1433-0407