Frontotemporal dementia
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Publisher
Elsevier
Reference269 articles.
1. One family, one gene and three phenotypes: a novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia;Abrahao;J Neurol Sci,2016
2. Cerebrovascular risk factors and triggers in transient global amnesia patients with and without jugular valve incompetence: results from a sample of 243 patients;Agosti;Eur Neurol,2010
3. Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy;Ajroud-Driss;Neurogenetics,2015
4. No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden;Akimoto;Amyotroph Lateral Scler Frontotemporal Degener,2013
5. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories;Akimoto;J Med Genet,2014
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1. A Peculiar Tau Accumulation Pattern Identified Via 18F-Florzolotau PET Imaging in a Patient With Frontotemporal Dementia Caused by a Mutation in the MAPT Gene;Clinical Nuclear Medicine;2024-07-15
2. Tau fibrils evade autophagy by excessive p62 coating and TAX1BP1 exclusion;Science Advances;2024-06-14
3. Human Endogenous Retroviruses in Neurodegenerative Diseases;Genes;2024-06-05
4. Identifying risk loci for FTD and shared genetic component with ALS: A large-scale multitrait association analysis;Neurobiology of Aging;2024-02
5. Lipid Dysregulation Unveil the Intricate Interplay of Lysosomal and Mitochondrial Changes in Frontotemporal Dementia with GRN Haploinsufficiency;2024-01-22
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