Torthaí cuardaigh - Matthis Synofzik
- 1 - 20 toradh as 144 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Affective coding: the emotional dimension of agency de réir Antje Gentsch, Matthis Synofzik
Foilsithe / Cruthaithe 2014Artigo -
2
Motor Training in Degenerative Spinocerebellar Disease: Ataxia-Specific Improvements by Intensive Physiotherapy and Exergames de réir Matthis Synofzik, Winfried Ilg
Foilsithe / Cruthaithe 2014Revisão -
3
Overcoming the divide between ataxias and spastic paraplegias: Shared phenotypes, genes, and pathways de réir Matthis Synofzik, Rebecca Schüle
Foilsithe / Cruthaithe 2017Revisão -
4
The Cerebellum Updates Predictions about the Visual Consequences of One's Behavior de réir Matthis Synofzik, Axel Lindner, Peter Thier
Foilsithe / Cruthaithe 2008Artigo -
5
The experience of agency: an interplay between prediction and postdiction de réir Matthis Synofzik, Gottfried Vosgerau, Martin Voss
Foilsithe / Cruthaithe 2013Artigo -
6
I move, therefore I am: A new theoretical framework to investigate agency and ownership de réir Matthis Synofzik, Gottfried Vosgerau, Albert Newen
Foilsithe / Cruthaithe 2008Artigo -
7
The Cerebellum Optimizes Perceptual Predictions about External Sensory Events de réir Manuel Jan Roth, Matthis Synofzik, Axel Lindner
Foilsithe / Cruthaithe 2013Artigo -
8
Autosomal Recessive Cerebellar Ataxias: Paving the Way toward Targeted Molecular Therapies de réir Matthis Synofzik, Hélène Puccio, Fanny Mochel, Lüdger Schöls
Foilsithe / Cruthaithe 2019Revisão -
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Scale for the Assessment and Rating of Ataxia (SARA): Development of a Training Tool and Certification Program de réir Marcus Grobe‐Einsler, Arian Taheri Amin, Jennifer Faber, Hartmut Völkel, Matthis Synofzik, Thomas Klockgether
Foilsithe / Cruthaithe 2023Artigo -
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Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxia de réir David Pellerin, Matt C. Danzi, M. Renaud, Henry Houlden, Matthis Synofzik, Stephan Züchner, Bernard Brais
Foilsithe / Cruthaithe 2024Revisão -
14
Fampridine and Acetazolamide in EA2 and Related Familial EA de réir Carolin Muth, Julian Teufel, Lüdger Schöls, Matthis Synofzik, Christiana Franke, Dagmar Timmann, Ulrich Mansmann, Michael Strupp
Foilsithe / Cruthaithe 2020Artigo -
15
Brain activation in frontotemporal and Alzheimer’s dementia: a functional near-infrared spectroscopy study de réir Florian G. Metzger, Betti Schopp, Florian B. Haeussinger, Katja Dehnen, Matthis Synofzik, Andreas J. Fallgatter, Ann‐Christine Ehlis
Foilsithe / Cruthaithe 2016Artigo -
16
As Frequent as Polyglutamine Spinocerebellar Ataxias: <scp>SCA27B</scp> in a Large German Autosomal Dominant Ataxia Cohort de réir Holger Hengel, David Pellerin, Carlo Wilke, Zofia Fleszar, Bernard Brais, Tobias B. Haack, Andreas Traschütz, Lüdger Schöls, Matthis Synofzik
Foilsithe / Cruthaithe 2023Carta -
17
Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort de réir Stefanie Krüger, Florian Battke, Andrea Sprecher, Marita Munz, Matthis Synofzik, Lüdger Schöls, Thomas Gasser, Torsten Grehl, Johannes Prudlo, Saskia Biskup
Foilsithe / Cruthaithe 2016Artigo -
18
Systemic inflammation relates to neuroaxonal damage associated with long-term cognitive dysfunction in COVID-19 patients de réir Harmke B. Duindam, David Mengel, Matthijs Kox, Jens Göpfert, Roy P. C. Kessels, Matthis Synofzik, Peter Pickkers, Wilson F. Abdo
Foilsithe / Cruthaithe 2024Artigo -
19
Preparing n-of-1 Antisense Oligonucleotide Treatments for Rare Neurological Diseases in Europe: Genetic, Regulatory, and Ethical Perspectives de réir Matthis Synofzik, Willeke M. C. van Roon‐Mom, Georg Marckmann, Hermine A. van Duyvenvoorde, Holm Graeßner, Rebecca Schüle, Annemieke Aartsma‐Rus
Foilsithe / Cruthaithe 2021Artigo -
20
Real‐Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia de réir Annika Thierfelder, Jens Seemann, Natalie John, Florian Harmuth, Martin A. Giese, Rebecca Schüle, Lüdger Schöls, Dagmar Timmann, Matthis Synofzik, Winfried Ilg
Foilsithe / Cruthaithe 2022Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Medicine
Biology
Genetics
Neuroscience
Disease
Pathology
Psychology
Internal medicine
Ataxia
Gene
Psychiatry
Dementia
Frontotemporal dementia
Spinocerebellar ataxia
Cerebellar ataxia
Phenotype
Mutation
Cohort
Physical medicine and rehabilitation
Allele
C9orf72
Atrophy
Trinucleotide repeat expansion
Biomarker
Neurodegeneration
Pediatrics
Oncology
Cognition
Frontotemporal lobar degeneration
Missense mutation