Результати пошуку - Matthis Synofzik
- Показ 1 - 20 результатів із 144
- На наступну сторінку
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Affective coding: the emotional dimension of agency за авторством Antje Gentsch, Matthis Synofzik
Опубліковано 2014Artigo -
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Overcoming the divide between ataxias and spastic paraplegias: Shared phenotypes, genes, and pathways за авторством Matthis Synofzik, Rebecca Schüle
Опубліковано 2017Revisão -
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The Cerebellum Updates Predictions about the Visual Consequences of One's Behavior за авторством Matthis Synofzik, Axel Lindner, Peter Thier
Опубліковано 2008Artigo -
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The experience of agency: an interplay between prediction and postdiction за авторством Matthis Synofzik, Gottfried Vosgerau, Martin Voss
Опубліковано 2013Artigo -
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I move, therefore I am: A new theoretical framework to investigate agency and ownership за авторством Matthis Synofzik, Gottfried Vosgerau, Albert Newen
Опубліковано 2008Artigo -
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The Cerebellum Optimizes Perceptual Predictions about External Sensory Events за авторством Manuel Jan Roth, Matthis Synofzik, Axel Lindner
Опубліковано 2013Artigo -
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Autosomal Recessive Cerebellar Ataxias: Paving the Way toward Targeted Molecular Therapies за авторством Matthis Synofzik, Hélène Puccio, Fanny Mochel, Lüdger Schöls
Опубліковано 2019Revisão -
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Scale for the Assessment and Rating of Ataxia (SARA): Development of a Training Tool and Certification Program за авторством Marcus Grobe‐Einsler, Arian Taheri Amin, Jennifer Faber, Hartmut Völkel, Matthis Synofzik, Thomas Klockgether
Опубліковано 2023Artigo -
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Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxia за авторством David Pellerin, Matt C. Danzi, M. Renaud, Henry Houlden, Matthis Synofzik, Stephan Züchner, Bernard Brais
Опубліковано 2024Revisão -
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Fampridine and Acetazolamide in EA2 and Related Familial EA за авторством Carolin Muth, Julian Teufel, Lüdger Schöls, Matthis Synofzik, Christiana Franke, Dagmar Timmann, Ulrich Mansmann, Michael Strupp
Опубліковано 2020Artigo -
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Brain activation in frontotemporal and Alzheimer’s dementia: a functional near-infrared spectroscopy study за авторством Florian G. Metzger, Betti Schopp, Florian B. Haeussinger, Katja Dehnen, Matthis Synofzik, Andreas J. Fallgatter, Ann‐Christine Ehlis
Опубліковано 2016Artigo -
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As Frequent as Polyglutamine Spinocerebellar Ataxias: <scp>SCA27B</scp> in a Large German Autosomal Dominant Ataxia Cohort за авторством Holger Hengel, David Pellerin, Carlo Wilke, Zofia Fleszar, Bernard Brais, Tobias B. Haack, Andreas Traschütz, Lüdger Schöls, Matthis Synofzik
Опубліковано 2023Carta -
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Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort за авторством Stefanie Krüger, Florian Battke, Andrea Sprecher, Marita Munz, Matthis Synofzik, Lüdger Schöls, Thomas Gasser, Torsten Grehl, Johannes Prudlo, Saskia Biskup
Опубліковано 2016Artigo -
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Systemic inflammation relates to neuroaxonal damage associated with long-term cognitive dysfunction in COVID-19 patients за авторством Harmke B. Duindam, David Mengel, Matthijs Kox, Jens Göpfert, Roy P. C. Kessels, Matthis Synofzik, Peter Pickkers, Wilson F. Abdo
Опубліковано 2024Artigo -
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Preparing n-of-1 Antisense Oligonucleotide Treatments for Rare Neurological Diseases in Europe: Genetic, Regulatory, and Ethical Perspectives за авторством Matthis Synofzik, Willeke M. C. van Roon‐Mom, Georg Marckmann, Hermine A. van Duyvenvoorde, Holm Graeßner, Rebecca Schüle, Annemieke Aartsma‐Rus
Опубліковано 2021Artigo -
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Real‐Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia за авторством Annika Thierfelder, Jens Seemann, Natalie John, Florian Harmuth, Martin A. Giese, Rebecca Schüle, Lüdger Schöls, Dagmar Timmann, Matthis Synofzik, Winfried Ilg
Опубліковано 2022Artigo
Інструменти для пошуку:
Пов'язані теми
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