Authors: Deschauer, M Muller, T Dreha, S Zierz, S

Citation: M. Deschauer et al., Familial mitochondrial chronic progressive external ophthalmoplegia. Five families with different genetics, NERVENARZT, 72(2), 2001, pp. 122-129

Authors: Deschauer, M Muller, T Wieser, T Schulte-Mattler, W Kornhuber, M Zierz, S

Citation: M. Deschauer et al., Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation, ARCH NEUROL, 58(11), 2001, pp. 1885-1888

Authors: Schulte-Mattler, WJ Deschauer, M Kornhuber, M Zierz, S

Citation: Wj. Schulte-mattler et al., Abnormal late responses upon transcranial magnetic stimulation in patientswith Stiff Man Syndrome, KLIN NEUROP, 31(2), 2000, pp. 59-64

Authors: Deschauer, M Neudecker, S Muller, T Gellerich, FN Zierz, S

Citation: M. Deschauer et al., Higher proportion of mitochondrial A3243G mutation in blood than in skeletal muscle in a patient with cardiomyopathy and hearing loss, MOL GEN MET, 70(3), 2000, pp. 235-237

Authors: Deschauer, M Stephan, M Stuhltrager, U Holzhausen, HJ Duncker, G Zierz, S

Citation: M. Deschauer et al., Bilateral inferior hemianopsia as initial symptom in Creutzfeldt-Jakob disease (Heidenhain type), KLIN MONATS, 216(4), 2000, pp. 227

Authors: Deschauer, M Wieser, T Neudecker, S Lindner, A Zierz, S

Citation: M. Deschauer et al., Mitochondrial 3243 A -> G mutation (MELAS mutation) associated with painful muscle stiffness, NEUROMUSC D, 9(5), 1999, pp. 305-307