Home > Authorities > Institutes > Record #141778 |
AG Maetzler
Functional Neurogeriatrics Also known as:AG Maetzler; AG MätzlerID | I:(DE-2719)5000024 |
All known publications ...
Download: BibTeX | EndNote XML, Text | RIS |
Journal Article
Acute changes in systemic glycemia gate access and action of GLP-1R agonist on brain structures controlling energy homeostasis.
Cell reports 41(8), 111698 (2022) [10.1016/j.celrep.2022.111698]
Files
Fulltext by Pubmed Central
BibTeX |
EndNote:
XML,
Text |
RIS
Journal Article
Detection of spinal long fiber tract degeneration in HSP: Improved diffusion tensor imaging.
NeuroImage: Clinical 36, 103213 (2022) [10.1016/j.nicl.2022.103213]
Files
Fulltext by Pubmed Central
BibTeX |
EndNote:
XML,
Text |
RIS
Journal Article
Inertial Gait Sensors to Measure Mobility and Functioning in Hereditary Spastic Paraplegia: A Cross-Sectional Multicenter Clinical Study
Neurology 99(10), e1079 - e1089 (2022) [10.1212/WNL.0000000000200819]
BibTeX |
EndNote:
XML,
Text |
RIS
Journal Article
Levels of Neurofilament Light at the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type 1
Neurology 98(20), e1985 - e1996 (2022) [10.1212/WNL.0000000000200257]
Fulltext by Pubmed Central
BibTeX |
EndNote:
XML,
Text |
RIS
Journal Article
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 (2022) [10.1089/nat.2021.0039]
Files
Fulltext by Pubmed Central
BibTeX |
EndNote:
XML,
Text |
RIS
Journal Article
Real-Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia.
Movement disorders 37(5), 1047-1058 (2022) [10.1002/mds.28930]
Files
BibTeX |
EndNote:
XML,
Text |
RIS
Journal Article
Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders.
eLife 10, e70905 (2021) [10.7554/eLife.70905]
Files
Fulltext by Pubmed Central
BibTeX |
EndNote:
XML,
Text |
RIS
Journal Article (Erratum/Correction)
Correction: Solving unsolved rare neurological diseases-a Solve-RD viewpoint.
European journal of human genetics 29(9), 1462 - 1465 (2021) [10.1038/s41431-021-00935-5]
Fulltext by Pubmed Central
BibTeX |
EndNote:
XML,
Text |
RIS
Journal Article (Erratum/Correction)
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 (2021) [10.1038/s41431-021-00936-4]
Fulltext by Pubmed Central
BibTeX |
EndNote:
XML,
Text |
RIS
Journal Article
Neurofilament light chain is a cerebrospinal fluid biomarker in hereditary spastic paraplegia.
Annals of Clinical and Translational Neurology 8(5), 1122 - 1131 (2021) [10.1002/acn3.51358]
Files
Fulltext by Pubmed Central
BibTeX |
EndNote:
XML,
Text |
RIS
All known publications ...
Download: BibTeX | EndNote XML, Text | RIS |