Selected Publications

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System Comparison for Gait and Balance Monitoring Used for the Evaluation of a Home-Based Training
Sensors 22(13), 4975 - () [10.3390/s22134975] OpenAccess  Download fulltext Files  Download fulltextFulltext by OpenAccess repository BibTeX | EndNote: XML, Text | RIS

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Regional changes of brain structure during progression of idiopathic Parkinson's disease – A longitudinal study using deformation based morphometry
Cortex 151, 188 - 210 () [10.1016/j.cortex.2022.03.009] OpenAccess  Download fulltext Files  Download fulltextFulltext by OpenAccess repository BibTeX | EndNote: XML, Text | RIS

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Spinocerebellar ataxia type 14: Refining clinico-genetic diagnosis in a rare adult-onset disorder
Annals of Clinical and Translational Neurology 8(4), 774-789 () [10.1002/acn3.51315] OpenAccess  Download fulltext Files  Download fulltextFulltext by OpenAccess repository BibTeX | EndNote: XML, Text | RIS

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Reference values for the Cerebellar Cognitive Affective / Schahmann Syndrome Scale: Age and education matter
Brain 144(2), e20 () [10.1093/brain/awaa417] Embargoed OpenAccess  Download fulltext Files  Download fulltextFulltext by OpenAccess repository BibTeX | EndNote: XML, Text | RIS

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Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
Brain 140(6), 1561 - 1578 () [10.1093/brain/awx095]  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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Cytoarchitectonic mapping of the human brain cerebellar nuclei in stereotaxic space and delineation of their co-activation patterns
Frontiers in neuroanatomy 09, 54 () [10.3389/fnana.2015.00054] OpenAccess  Download fulltext Files  Download fulltextFulltext by OpenAccess repository BibTeX | EndNote: XML, Text | RIS

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Autosomal Recessive Cerebellar Ataxia 3 Due to Homozygote c.132dupA Mutation Within the ANO10 Gene.
JAMA neurology 72(2), 238 -239 () [10.1001/jamaneurol.2014.3918] BibTeX | EndNote: XML, Text | RIS

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Progressive cognitive dysfunction in spinocerebellar ataxia type 3
Movement disorders 28(10), 1435–1438 () [10.1002/mds.25512]  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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The brain Myotonic Dystrophy 1 and 2: evidence for a predominant white matter disease
Brain 134, 3527 - 3543 () [10.1093/brain/awr299] pmc   Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Callosal tissue loss in Multiple System Atrophy - a follow-up study
Movement disorders 25, 2613- 2620 () [10.1002/mds.23318] pmc   Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

Last Modified: 13.02.2023