Michael David Geschwind
Affiliations: | University of California, San Francisco, San Francisco, CA |
Area:
prions, dementia, rapidly progressive dementia, Jakob-Creutzfeldt disease, autoimmune encephalopathyGoogle:
"Michael Geschwind"Mean distance: 106866
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Publications
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| Schmitz M, Villar-Piqué A, Hermann P, et al. (2022) Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases. Brain : a Journal of Neurology |
| Jones E, Hummerich H, Viré E, et al. (2020) Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study. The Lancet. Neurology. 19: 840-848 |
| Yang CY, Lai RY, Amokrane N, et al. (2020) Dysphagia in spinocerebellar ataxias type 1, 2, 3 and 6. Journal of the Neurological Sciences. 415: 116878 |
| Gan SR, Figueroa KP, Xu HL, et al. (2020) The impact of ethnicity on the clinical presentations of spinocerebellar ataxia type 3. Parkinsonism & Related Disorders. 72: 37-43 |
| Ngo KJ, Rexach JE, Lee H, et al. (2019) A Diagnostic Ceiling for Exome Sequencing in Cerebellar Ataxia and Related Neurological Disorders. Human Mutation |
| Aguilar-Calvo P, Sevillano AM, Bapat J, et al. (2019) Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions. Acta Neuropathologica |
| Minikel EV, Vallabh SM, Orseth MC, et al. (2019) Age at onset in genetic prion disease and the design of preventive clinical trials. Neurology |
| Staffaroni AM, Kramer AO, Casey M, et al. (2019) Association of Blood and Cerebrospinal Fluid Tau Level and Other Biomarkers With Survival Time in Sporadic Creutzfeldt-Jakob Disease. Jama Neurology |
| Vallabh SM, Nobuhara CK, Llorens F, et al. (2019) Prion protein quantification in human cerebrospinal fluid as a tool for prion disease drug development. Proceedings of the National Academy of Sciences of the United States of America |
| Vitali P, Palesi F, Cotta Ramusino M, et al. (2019) Early cortical and late striatal diffusion restriction on 3T MRI in a long-lived sporadic creutzfeldt-jakob disease case. Journal of Magnetic Resonance Imaging : Jmri |