Resultados da busca - Matthis Synofzik
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Affective coding: the emotional dimension of agency por Antje Gentsch, Matthis Synofzik
Publicado em 2014Artigo -
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As Frequent as Polyglutamine Spinocerebellar Ataxias: <scp>SCA27B</scp> in a Large German Autosomal Dominant Ataxia Cohort por Holger Hengel, David Pellerin, Carlo Wilke, Zofia Fleszar, Bernard Brais, Tobias B. Haack, Andreas Traschütz, Lüdger Schöls, Matthis Synofzik
Publicado em 2023Carta -
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Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort por Stefanie Krüger, Florian Battke, Andrea Sprecher, Marita Munz, Matthis Synofzik, Lüdger Schöls, Thomas Gasser, Torsten Grehl, Johannes Prudlo, Saskia Biskup
Publicado em 2016Artigo -
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Systemic inflammation relates to neuroaxonal damage associated with long-term cognitive dysfunction in COVID-19 patients por Harmke B. Duindam, David Mengel, Matthijs Kox, Jens Göpfert, Roy P. C. Kessels, Matthis Synofzik, Peter Pickkers, Wilson F. Abdo
Publicado em 2024Artigo -
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Preparing n-of-1 Antisense Oligonucleotide Treatments for Rare Neurological Diseases in Europe: Genetic, Regulatory, and Ethical Perspectives por Matthis Synofzik, Willeke M. C. van Roon‐Mom, Georg Marckmann, Hermine A. van Duyvenvoorde, Holm Graeßner, Rebecca Schüle, Annemieke Aartsma‐Rus
Publicado em 2021Artigo -
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Real‐Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia por Annika Thierfelder, Jens Seemann, Natalie John, Florian Harmuth, Martin A. Giese, Rebecca Schüle, Lüdger Schöls, Dagmar Timmann, Matthis Synofzik, Winfried Ilg
Publicado em 2022Artigo
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Medicine
Biology
Genetics
Neuroscience
Disease
Pathology
Psychology
Internal medicine
Ataxia
Gene
Psychiatry
Dementia
Frontotemporal dementia
Spinocerebellar ataxia
Cerebellar ataxia
Phenotype
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Cohort
Physical medicine and rehabilitation
Allele
C9orf72
Atrophy
Trinucleotide repeat expansion
Biomarker
Neurodegeneration
Pediatrics
Oncology
Cognition
Frontotemporal lobar degeneration
Missense mutation