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Language and Speech Markers of Primary Progressive Aphasia: A Systematic Review.
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- American Journal of Speech-Language Pathology, 2020, v. 29, n. 4, p. 2206, doi. 10.1044/2020_AJSLP-20-00008
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- Article
Therapy-Induced Electrophysiological Changes in Primary Progressive Aphasia: A Preliminary Study.
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- Frontiers in Human Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fnhum.2022.766866
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- Article
The Electrophysiological Correlates of Phoneme Perception in Primary Progressive Aphasia: A Preliminary Case Series.
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- Frontiers in Human Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnhum.2021.618549
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- Article
The genetics and neuropathology of frontotemporal lobar degeneration.
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- Acta Neuropathologica, 2012, v. 124, n. 3, p. 353, doi. 10.1007/s00401-012-1029-x
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- Article
A case series of verbal semantic processing in primary progressive aphasia: Evidence from the N400 effect.
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- International Journal of Language & Communication Disorders, 2021, v. 56, n. 6, p. 1165, doi. 10.1111/1460-6984.12658
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- Article
Geographical frequency of the FTLD-ALS causing C9orf72 repeat expansion mutation in an extended cohort ascertained within the European consortium on early-onset dementia
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- 2012
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- Abstract
Genomic characterization of the C9orf72 promoter repeat in FTLD and ALS patients
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- 2012
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- Abstract
The clinical presentation of C9orf72-associated frontotemporal lobar degeneration in an extended Flanders-Belgian cohort
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- 2012
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- Abstract
Association of intermediate-length polyQ expansions in ATXN2 with ALS but not FTLD in a flanders-belgian cohort
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- 2011
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- Abstract
TMEM106B the first common risk factor for FTLD: Replication in a clinically diagnosed cohort of FTLD patients
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- 2010
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- Abstract
Extended FTLD pedigree segregating a Belgian <italic>GRN</italic>-null mutation: neuropathological heterogeneity in one family.
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- Alzheimer's Research & Therapy, 2018, v. 10, p. 1, doi. 10.1186/s13195-017-0334-y
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- Article
Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia.
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- Human Brain Mapping, 2023, v. 44, n. 7, p. 2684, doi. 10.1002/hbm.26220
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- Article
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.
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- 2016
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- journal article
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort.
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- Brain: A Journal of Neurology, 2011, v. 134, n. 3, p. 808, doi. 10.1093/brain/awr007
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- Article
A Pan- European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats.
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- Human Mutation, 2013, v. 34, n. 2, p. 363, doi. 10.1002/humu.22244
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- Article
Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion.
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- JAMA Neurology, 2017, v. 74, n. 4, p. 445, doi. 10.1001/jamaneurol.2016.4847
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- Article
Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort.
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- JAMA Neurology, 2013, v. 70, n. 3, p. 365, doi. 10.1001/2013.jamaneurol.181
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- Article
In‐depth phenotypic description of pathogenic TBK1 mutations: A frequent cause of FTD and ALS in the Flanders‐Belgian population.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.052900
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- Article