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Single-cell multimodal analysis in a case with reduced penetrance of Progranulin-Frontotemporal Dementia.
- Published in:
- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01234-2
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- Article
Association of novel CSF biomarker candidates with cortical thickness in genetic frontotemporal dementia.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.082525
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- Article
Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.
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- European Journal of Human Genetics, 2013, v. 21, n. 11, p. 1260, doi. 10.1038/ejhg.2013.37
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- Article
Novel CSF biomarkers in genetic frontotemporal dementia identified by proteomics.
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- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 4, p. 698, doi. 10.1002/acn3.745
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- Article
Neurofilament light chain: a biomarker for genetic frontotemporal dementia.
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- Annals of Clinical & Translational Neurology, 2016, v. 3, n. 8, p. 623, doi. 10.1002/acn3.325
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- Article
Repeated cognitive assessments show stable function over time in patients with ALS.
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- Journal of Neurology, 2024, v. 271, n. 8, p. 5267, doi. 10.1007/s00415-024-12479-x
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- Article
TBK1 haploinsufficiency results in changes in the K63-ubiquitination profiles in brain and fibroblasts from affected and presymptomatic mutation carriers.
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- Journal of Neurology, 2022, v. 269, n. 6, p. 3037, doi. 10.1007/s00415-021-10887-x
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- Article
Altered levels of CSF proteins in patients with FTD, presymptomatic mutation carriers and non-carriers.
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- Translational Neurodegeneration, 2020, v. 9, n. 1, p. 1, doi. 10.1186/s40035-020-00198-y
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- Article
The usage of population and disease registries as pre-screening tools for clinical trials, a systematic review.
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- Systematic Reviews, 2024, v. 13, p. 1, doi. 10.1186/s13643-024-02533-0
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- Article
Altered plasma protein profiles in genetic FTD – a GENFI study.
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- Molecular Neurodegeneration, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13024-023-00677-6
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- Article
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study.
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- Molecular Neurodegeneration, 2021, v. 16, n. 1, p. 1, doi. 10.1186/s13024-021-00499-4
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- Article