Found: 27
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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.
- Published in:
- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01121-w
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- Publication type:
- Article
Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 4, p. 1624, doi. 10.1093/brain/awac362
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- Publication type:
- Article
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.
- Published in:
- 2016
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- Publication type:
- journal article
Microtubule associated protein tau p.R406W patient carriers present with a nonconforming clinical phenotype.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 3, p. 1, doi. 10.1002/alz.067779
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- Publication type:
- Article
Extensive genetic and phenotypic description of MAPT p.R406W in the Flanders‐Belgian population.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.053069
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- Publication type:
- Article
In‐depth phenotypic description of pathogenic TBK1 mutations: A frequent cause of FTD and ALS in the Flanders‐Belgian population.
- Published in:
- 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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- Publication type:
- Article
P1‐210: INVESTIGATING THE INVOLVEMENT OF THE DPP6‐KV4.2 PROTEIN COMPLEX IN DEMENTIA.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P316, doi. 10.1016/j.jalz.2019.06.765
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- Publication type:
- Article
P3‐128: EXPLORING THE MOLECULAR MECHANISM OF NEURONAL HYPEREXCITABILITY IN DEMENTIA.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1116, doi. 10.1016/j.jalz.2018.06.1485
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- Publication type:
- Article
P3‐121: RARE FRAMESHIFT AND DIGENIC MUTATIONS CONTRIBUTE TO DISEASE ETIOLOGY IN BELGIAN ALZHEIMER AND FRONTOTEMPORAL DEMENTIA PATIENTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1113, doi. 10.1016/j.jalz.2018.06.1478
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- Publication type:
- Article
Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration.
- Published in:
- Alzheimer's Research & Therapy, 2018, v. 10, p. 1, doi. 10.1186/s13195-018-0364-0
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- Publication type:
- Article
Extended FTLD pedigree segregating a Belgian <italic>GRN</italic>-null mutation: neuropathological heterogeneity in one family.
- Published in:
- Alzheimer's Research & Therapy, 2018, v. 10, p. 1, doi. 10.1186/s13195-017-0334-y
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- Publication type:
- Article
A PROSPECTIVE NEUROGENETIC STUDY ON EARLY-ONSET DEMENTIA IN PATIENTS WITH UNCLEAR INITIAL DIAGNOSIS OF DEGENERATIVE DEMENTIA.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1284, doi. 10.1016/j.jalz.2017.06.1934
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- Publication type:
- Article
NEK1 GENETIC VARIABILITY IN A BELGIAN COHORT OF ALS AND FTD-ALS PATIENTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1284, doi. 10.1016/j.jalz.2017.06.1935
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- Publication type:
- Article
THE MAPT P.ARG406TRP IS A FOUNDER MUTATION IN BELGIUM AND PRESENTS WITH AN ALZHEIMER DISEASE DEMENTIA-LIKE PHENOTYPE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1286, doi. 10.1016/j.jalz.2017.06.1940
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- Publication type:
- Article
INCREASED CSF LEVELS OF BIOMARKERS FOR NEURODEGENERATION IN FTLD-GRN MUTATION CARRIERS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P1058, doi. 10.1016/j.jalz.2016.06.2211
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- Publication type:
- Article
DIAGNOSTIC PERFORMANCE OF NON-PHOSPHORYLATED TAU FRACTION (PTAU REL) IN CSF AS BIOMARKER FOR DIFFERENTIAL DEMENTIA DIAGNOSIS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P672, doi. 10.1016/j.jalz.2016.06.1320
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- Publication type:
- Article
CSF EXPLORATORY BIOMARKER STUDY FOR (DIFFERENTIAL) DIAGNOSIS OF FRONTOTEMPORAL LOBAR DEGENERATION.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P471, doi. 10.1016/j.jalz.2016.06.924
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- Publication type:
- Article
EEG DOMINANT FREQUENCY PEAK DIFFERENTIATES BETWEEN ALZHEIMER'S DISEASE AND FRONTOTEMPORAL LOBAR DEGENERATION.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P354, doi. 10.1016/j.jalz.2016.06.656
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- Publication type:
- Article
DISCORDANCE BETWEEN AMYLOID-PET AND CSF AMYLOID-β FOR DIAGNOSING ALZHEIMER’S DISEASE IN A CLINICAL SETTING.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P1154, doi. 10.1016/j.jalz.2016.07.057
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- Publication type:
- Article
CSF BIOMARKERS TO PREDICT RATE OF COGNITIVE DECLINE IN ALZHEIMER’S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P1157, doi. 10.1016/j.jalz.2016.07.066
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- Publication type:
- Article
Loss-of-function mutations in TBK1 are frequently associated with frontotemporal lobar degeneration in a belgian patient cohort.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P333, doi. 10.1016/j.jalz.2015.08.157
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- Publication type:
- Article
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.
- Published in:
- Acta Neuropathologica Communications, 2015, v. 3, p. 1, doi. 10.1186/s40478-015-0246-7
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- Publication type:
- Article
Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion.
- Published in:
- JAMA Neurology, 2017, v. 74, n. 4, p. 445, doi. 10.1001/jamaneurol.2016.4847
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- Publication type:
- Article
No added diagnostic value of non-phosphorylated tau fraction (p-tau<sub>rel</sub>) in CSF as a biomarker for differential dementia diagnosis.
- Published in:
- Alzheimer's Research & Therapy, 2017, v. 9, p. 1, doi. 10.1186/s13195-017-0275-5
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- Publication type:
- Article
Tacrolimus-induced cognitive impairment: a case report.
- Published in:
- 2024
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- Publication type:
- Letter
Validation of the Semiquantitative Static SUVR Method for <sup>18</sup>F-AV45 PET by Pharmacokinetic Modeling with an Arterial Input Function.
- Published in:
- Journal of Nuclear Medicine, 2017, v. 58, n. 9, p. 1483, doi. 10.2967/jnumed.116.184481
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- Publication type:
- Article
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.
- Published in:
- Acta Neuropathologica, 2019, v. 137, n. 6, p. 901, doi. 10.1007/s00401-019-01976-3
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- Publication type:
- Article