Matthis Synofzik

CSF Aβ42 and tau in Parkinson's disease with cognitive impairment

L. Schöls, M. Synofzik, C. Schulte, 2010, Movement disorders : official journal of the Movement Disorder Society.

Autosomal Recessive Cerebellar Ataxias: Paving the Way toward Targeted Molecular Therapies

L. Schöls, M. Synofzik, F. Mochel, 2019, Neuron.

Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia

J. Winkler, S. Klebe, P. Bauer, 2009, Journal of Neurology, Neurosurgery & Psychiatry.

I Move, Therefore I Am: a New Theoretical Framework to Investigate Agency and Ownership Consciousness and Cognition

A. Newen, G. Vosgerau, Matthis Synofzik, 2022 .

Advancing molecular, phenotypic and mechanistic insights of FGF14 pathogenic expansions (SCA27B)

S. Klebe, U. Roggenbuck, S. Pechlivanis, 2024, medRxiv.

PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

S. Züchner, Michael A. Gonzalez, E. Battaloğlu, 2017, Clinical genetics.

Scholarship@Western Scholarship@Western

M. Grosse-Wentrup, J. Gómez-Pilar, Shumei Cao, 2022 .

Coordination and timing deficits in speech and swallowing in autosomal recessive spastic ataxia of Charlevoix–Saguenay (ARSACS)

Elsdon Storey, Adam P Vogel, Matthis Synofzik, 2018, Journal of Neurology.