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31. Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegia. (December 2020)

32. Levels of Neurofilament Light at the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type 1. (17th May 2022)

33. Levels of Neurofilament Light at the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type 1. (17th May 2022)

34. Linkage and Association Analysis Identifies TRAF1 Influencing Common Carotid Intima–Media Thickness. Issue 12 (December 2016)

36. Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study. Issue 11 (November 2015)

37. Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with SPG7. (4th June 2019)