Bilaketaren emaitzak - Matthis Synofzik
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Affective coding: the emotional dimension of agency nork Antje Gentsch, Matthis Synofzik
Argitaratua 2014Artigo -
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The Cerebellum Updates Predictions about the Visual Consequences of One's Behavior nork Matthis Synofzik, Axel Lindner, Peter Thier
Argitaratua 2008Artigo -
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The experience of agency: an interplay between prediction and postdiction nork Matthis Synofzik, Gottfried Vosgerau, Martin Voss
Argitaratua 2013Artigo -
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The Cerebellum Optimizes Perceptual Predictions about External Sensory Events nork Manuel Jan Roth, Matthis Synofzik, Axel Lindner
Argitaratua 2013Artigo -
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As Frequent as Polyglutamine Spinocerebellar Ataxias: <scp>SCA27B</scp> in a Large German Autosomal Dominant Ataxia Cohort nork Holger Hengel, David Pellerin, Carlo Wilke, Zofia Fleszar, Bernard Brais, Tobias B. Haack, Andreas Traschütz, Lüdger Schöls, Matthis Synofzik
Argitaratua 2023Carta -
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Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort nork Stefanie Krüger, Florian Battke, Andrea Sprecher, Marita Munz, Matthis Synofzik, Lüdger Schöls, Thomas Gasser, Torsten Grehl, Johannes Prudlo, Saskia Biskup
Argitaratua 2016Artigo -
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Preparing n-of-1 Antisense Oligonucleotide Treatments for Rare Neurological Diseases in Europe: Genetic, Regulatory, and Ethical Perspectives nork Matthis Synofzik, Willeke M. C. van Roon‐Mom, Georg Marckmann, Hermine A. van Duyvenvoorde, Holm Graeßner, Rebecca Schüle, Annemieke Aartsma‐Rus
Argitaratua 2021Artigo -
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Real‐Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia nork Annika Thierfelder, Jens Seemann, Natalie John, Florian Harmuth, Martin A. Giese, Rebecca Schüle, Lüdger Schöls, Dagmar Timmann, Matthis Synofzik, Winfried Ilg
Argitaratua 2022Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
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