Jung, Hans H.

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Moss, D. J. H., Pardiñas, A. F., Langbehn, D., Lo, K., Leavitt, B. R., Roos, R., Durr, A., Mead, S., Coleman, A., Santos, R. D., et al. (2017) · The Lancet Neurology

Genetic Neurodegenerative DiseasesGenetic Associations and Epidemiology

Cited by 312

Biochemical diagnosis of Alzheimer disease by measuring the cerebrospinal fluid ratio of phosphorylated tau protein to β-amyloid peptide42

Maddalena, A., Papassotiropoulos, A., Müller-Tillmanns, B., Jung, H. H., Hegi, T., Nitsch, R. M., & Hock, C. (2003) · Archives of Neurology

Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatments

Cited by 204

Exercise effects in Huntington disease

Frese, S., Petersen, J. A., Ligon-Auer, M., Mueller, S. M., Mihaylova, V., Gehrig, S. M., Kana, V., Rushing, E. J., Unterburger, E., Kägi, G., et al. (2017) · Journal of Neurology

Genetic Neurodegenerative DiseasesPhysical Activity and Health

Cited by 46

Exercise in Huntington’s Disease: Current State and Clinical Significance

Mueller, S. M., Petersen, J. A., & Jung, H. H. (2019) · Tremor and Other Hyperkinetic Movements

Genetic Neurodegenerative DiseasesPhysical Activity and Health

Cited by 40