Vielhaber, Stefan

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients

Schüle, R., Wiethoff, S., Martus, P., Karle, K. N., Otto, S., Klebe, S., Klimpe, S., Gallenmüller, C., Kurzwelly, D., Henkel, D., et al. (2016) · Annals of Neurology

Hereditary Neurological DisordersGenetic Neurodegenerative Diseases

Cited by 315

Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis

Wiedemann, F. R., Winkler, K., Kuznetsov, A. V., Bartels, C., Vielhaber, S., Feistner, H., & Kunz, W. S. (1998) · Journal of the Neurological Sciences

Amyotrophic Lateral Sclerosis ResearchMitochondrial Function and Pathology

Cited by 262

Health-related quality of life in ALS, myasthenia gravis and facioscapulohumeral muscular dystrophy

Winter, Y., Schepelmann, K., Spottke, A. E., Claus, D., Grothe, C., Schröder, R., Heuss, D., Vielhaber, S., Tackenberg, B., Mylius, V., et al. (2010) · Journal of Neurology

Neurogenetic and Muscular Disorders ResearchHealth Systems, Economic Evaluations, Quality of Life

Cited by 86

Information needs and information-seeking preferences of ALS patients and their carers

Abdulla, S., Vielhaber, S., Machts, J., Heinze, H.-J., Dengler, R., & Petri, S. (2014) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Health Literacy and Information AccessibilityAmyotrophic Lateral Sclerosis Research

Cited by 42