AG Maetzler

Functional Neurogeriatrics Also known as:AG Maetzler; AG Mätzler
IDI:(DE-2719)5000024

TÜ DZNE

Recent Publications

All known publications ...
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Acute changes in systemic glycemia gate access and action of GLP-1R agonist on brain structures controlling energy homeostasis.
Cell reports 41(8), 111698 () [10.1016/j.celrep.2022.111698] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Detection of spinal long fiber tract degeneration in HSP: Improved diffusion tensor imaging.
NeuroImage: Clinical 36, 103213 () [10.1016/j.nicl.2022.103213] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Inertial Gait Sensors to Measure Mobility and Functioning in Hereditary Spastic Paraplegia: A Cross-Sectional Multicenter Clinical Study
Neurology 99(10), e1079 - e1089 () [10.1212/WNL.0000000000200819] BibTeX | EndNote: XML, Text | RIS

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Levels of Neurofilament Light at the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type 1
Neurology 98(20), e1985 - e1996 () [10.1212/WNL.0000000000200257] pmc   Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Preparing n-of-1 Antisense Oligonucleotide Treatments for Rare Neurological Diseases in Europe: Genetic, Regulatory, and Ethical Perspectives.
Nucleic acid therapeutics 32(2), 83 - 94 () [10.1089/nat.2021.0039] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Real-Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia.
Movement disorders 37(5), 1047-1058 () [10.1002/mds.28930] OpenAccess  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders.
eLife 10, e70905 () [10.7554/eLife.70905] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Correction: Solving unsolved rare neurological diseases-a Solve-RD viewpoint.
European journal of human genetics 29(9), 1462 - 1465 () [10.1038/s41431-021-00935-5] pmc   Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases.
European journal of human genetics 29(9), 1459 - 1461 () [10.1038/s41431-021-00936-4] pmc   Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Neurofilament light chain is a cerebrospinal fluid biomarker in hereditary spastic paraplegia.
Annals of Clinical and Translational Neurology 8(5), 1122 - 1131 () [10.1002/acn3.51358] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

All known publications ...
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 Record created 2020-03-10, last modified 2024-09-06



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