Christoph Kamm

The natural history of multiple system atrophy: a prospective European cohort study

Gregor K. Wenning, Felix Geser, Florian Krismer et al. · The Lancet Neurology · 2013 · 518 citations · Full text

GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak

Yvonne Weber, Alexander Storch, Thomas V. Wuttke et al. · Journal of Clinical Investigation · 2008 · 354 citations · Full text

Electrolyte Disorder, Glut1 Mutations, Pathology +19

Nusinersen in adults with 5q spinal muscular atrophy: a non-interventional, multicentre, observational cohort study

Tim Hagenacker, Claudia D. Wurster, René Günther et al. · The Lancet Neurology · 2020 · 345 citations · Full text

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients

Rebecca Schüle, Sarah Wiethoff, Peter Martus et al. · Annals of Neurology · 2016 · 298 citations

Presentation, diagnosis, and management of multiple system atrophy in Europe: Final analysis of the European multiple system atrophy registry

Martin Köllensperger, Felix Geser, Jean‐Pierre Ndayisaba et al. · Movement Disorders · 2010 · 251 citations

Motor Dysfunction, Neurological Disorder, Multiple System Atrophy +25