TÜ DZNE

DZNE Tübingen Site Also known as:TUE DZNE; TÜ DZNE
IDI:(DE-2719)6000008

Recent Publications

All known publications ...
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The state-of-the-art of N-of-1 therapies and the IRDiRC N-of-1 development roadmap.
Nature reviews / Drug discovery 24(1), 40 - 56 () [10.1038/s41573-024-01059-3]  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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Subtypes of cognitive impairment in cerebellar disease identified by cross-diagnostic cluster-analysis: results from a German multicenter study.
Journal of neurology 272(1), 83 () [10.1007/s00415-024-12831-1] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3.
Journal of neurology 272(1), 54 () [10.1007/s00415-024-12829-9] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Frequency and neuropathology of HTT repeat expansions in FTD/ALS: co-existence rather than causation.
Journal of neurology 272(1), 58 () [10.1007/s00415-024-12822-2] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Myelin basic protein and TREM2 quantification in the CSF of patients with Multiple System Atrophy and other Parkinsonian conditions.
Journal of neurology 272(1), 52 () [10.1007/s00415-024-12747-w] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Postural control in episodic ataxia type 2: no evidence for increased vestibular excitability
European journal of neurology 32(1), e16520 () [10.1111/ene.16520] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.
Nature medicine 31(2), 478 - 489 () [10.1038/s41591-024-03420-w] OpenAccess  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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The novel p.A30G SNCA pathogenic variant in Greek patients with familial and sporadic Parkinson's disease.
European journal of neurology 32(2), e16562 () [10.1111/ene.16562] OpenAccess  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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Amyotrophic lateral sclerosis caused by FUS mutations: advances with broad implications.
The lancet 24(2), 166 - 178 () [10.1016/S1474-4422(24)00517-9]  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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Arrayed CRISPR libraries for the genome-wide activation, deletion and silencing of human protein-coding genes.
Nature biomedical engineering 9(1), 127 - 148 () [10.1038/s41551-024-01278-4] OpenAccess  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

All known publications ...
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 Record created 2020-02-18, last modified 2024-08-16



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