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Frontotemporal dementia: a bridge between dementia and neuromuscular disease.
- Published in:
- Annals of the New York Academy of Sciences, 2015, v. 1338, n. 1, p. 71, doi. 10.1111/nyas.12638
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- Publication type:
- Article
Correction to: Loss of homeostatic microglial phenotype in CSF1R-related Leukoencephalopathy.
- Published in:
- 2020
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- Publication type:
- Correction Notice
Loss of homeostatic microglial phenotype in CSF1R-related Leukoencephalopathy.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-00947-0
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- Publication type:
- Article
Uncovering the distinct macro-scale anatomy of dysexecutive and behavioural degenerative diseases.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 4, p. 1483, doi. 10.1093/brain/awad356
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- Publication type:
- Article
C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypes.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4055, doi. 10.1093/brain/awad133
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- Publication type:
- Article
Shared brain transcriptomic signature in TDP-43 type A FTLD patients with or without GRN mutations.
- Published in:
- 2022
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- Publication type:
- journal article
Cortical and subcortical pathological burden and neuronal loss in an autopsy series of FTLD-TDP-type C.
- Published in:
- 2022
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- Publication type:
- journal article
Long-read targeted sequencing uncovers clinicopathological associations for C9orf72-linked diseases.
- Published in:
- 2021
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- Publication type:
- journal article
Reply: LATE to the PART-y.
- Published in:
- 2019
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- Publication type:
- Letter
Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report.
- Published in:
- 2019
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- Publication type:
- journal article
Ossified blood vessels in primary familial brain calcification elicit a neurotoxic astrocyte response.
- Published in:
- 2019
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- Publication type:
- journal article
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.
- Published in:
- 2018
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- Publication type:
- journal article
TMEM106B and myelination: rare leukodystrophy families reveal unexpected connections.
- Published in:
- 2017
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- Publication type:
- journal article
PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease.
- Published in:
- 2015
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- Publication type:
- commentary
Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion.
- Published in:
- 2014
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- Publication type:
- journal article
Familial relatedness in genetic frontotemporal dementia cohorts: findings from the international Frontotemporal Dementia Prevention Initiative.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.078637
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- Publication type:
- Article
Neurite‐based white matter alterations in MAPT mutation carriers: A multi‐shell diffusion MRI study in the ALLFTD consortium.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.076827
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- Publication type:
- Article
Assessing patterns of network degeneration in familial frontotemporal lobar degeneration using FDG‐PET and unsupervised machine learning.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.076725
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- Publication type:
- Article
Clinical value of CSF TMEM106B in familial and sporadic frontotemporal lobar degeneration.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.080210
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- Publication type:
- Article
Inferring genetic relatedness in a large, multisite frontotemporal dementia series: Data from the ALLFTD consortium.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.068040
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- Publication type:
- Article
Progression of neuropsychiatric symptoms in pre‐dementia GRN and C9orf72 mutation carriers.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, p. 1, doi. 10.1002/alz.056465
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- Publication type:
- Article
Quantitative TDP‐43 burden and distribution in old age: High and low probability of Alzheimer's disease and genetically confirmed FTLD‐TDP‐43.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.055704
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- Publication type:
- Article
MRI correlates of neuropsychiatric symptom progression in pre‐dementia GRN and C9orf72 mutation carriers.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, p. 1, doi. 10.1002/alz.056513
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- Publication type:
- Article
Neuroimaging and neuropsychological findings in MAPT N279K mutation phenoconverters: Neuropsychiatry and behavioral neurology/Behavioral neurology.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 6, p. 1, doi. 10.1002/alz.046759
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- Publication type:
- Article
Neuroimaging and neuropsychological findings in MAPT N279K mutation phenoconverters: Neuropsychiatry and behavioral neurology/Behavioral neurology.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.046759
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- Publication type:
- Article
P3‐364: RATES OF LOBAR ATROPHY IN ASYMPTOMATIC MAPT MUTATION CARRIERS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1085, doi. 10.1016/j.jalz.2019.06.3397
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- Publication type:
- Article
P2‐397: GYRIFICATION ABNORMALITIES IN PRESYMPTOMATIC C9ORF72 EXPANSION CARRIERS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P758, doi. 10.1016/j.jalz.2019.06.2804
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- Publication type:
- Article
O2‐10‐02: WHOLE EXOME SEQUENCING ANALYSIS IN EARLY ONSET ALZHEIMER REVEALS NOVEL CANDIDATE GENES.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P564, doi. 10.1016/j.jalz.2019.06.4506
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- Publication type:
- Article
O2‐09‐06: TRAJECTORY OF LOBAR ATROPHY IN ASYMPTOMATIC AND SYMPTOMATIC GRN MUTATION CARRIERS: A LONGITUDINAL TBM‐SYN STUDY.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P563, doi. 10.1016/j.jalz.2019.06.4504
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- Publication type:
- Article
F2‐01‐01: NEURODEVELOPMENTAL DIFFERENCES AND ENVIRONMENTAL INSULTS INVERSELY CORRELATE WITH AGE OF ONSET IN ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P515, doi. 10.1016/j.jalz.2019.06.4416
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- Publication type:
- Article
O3‐06‐02: POLYGENIC SCORE ANALYSIS OF EXONIC VARIANTS IN AN IMMUNE CO‐REGULATORY NETWORK IDENTIFIES NOVEL PROTEIN‐ALTERING VARIANTS THAT ASSOCIATE WITH ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1025, doi. 10.1016/j.jalz.2018.06.2801
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- Publication type:
- Article
P2‐430: MR SPECTROSCOPY FROM FRONTAL LOBE AND POSTERIOR CINGULATE GYRUS IN ASYMPTOMATIC AND SYMPTOMATIC MICROTUBULE‐ASSOCIATED PROTEIN TAU (MAPT) MUTATION CARRIERS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P876, doi. 10.1016/j.jalz.2018.06.1122
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- Publication type:
- Article
P1‐420: ACCELERATED NEUROCHEMICAL CHANGES PRIOR TO PHENOCONVERSION TO FRONTOTEMPORAL LOBAR DEGENERATION IN PRESYMPTOMATIC MICROTUBULE‐ASSOCIATED PROTEIN TAU (MAPT) MUTATION CARRIERS: A LONGITUDINAL MRS STUDY.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P466, doi. 10.1016/j.jalz.2018.06.429
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- Publication type:
- Article
Brain MR Spectroscopy Changes Precede Frontotemporal Lobar Degeneration Phenoconversion in Mapt Mutation Carriers.
- Published in:
- 2019
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- Publication type:
- journal article
MRS in Early and Presymptomatic Carriers of a Novel Octapeptide Repeat Insertion in the Prion Protein Gene.
- Published in:
- Journal of Neuroimaging, 2013, v. 23, n. 3, p. 409, doi. 10.1111/j.1552-6569.2012.00717.x
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- Publication type:
- Article
Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review.
- Published in:
- Alzheimer's Research & Therapy, 2018, v. 10, p. 1, doi. 10.1186/s13195-017-0330-2
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- Publication type:
- Article
Early Neuropsychological Characteristics of Progranulin Mutation Carriers.
- Published in:
- Journal of the International Neuropsychological Society, 2014, v. 20, n. 7, p. 694, doi. 10.1017/S1355617714000551
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- Publication type:
- Article
TDP-43 PATHOLOGY DISRUPTS NUCLEAR PORE COMPLEXES AND NUCLEOCYTOPLASMIC TRANSPORT IN ALS/FTD.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P602, doi. 10.1016/j.jalz.2017.07.247
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- Publication type:
- Article
ABNORMAL CHROMOSOME COPY NUMBER AND ASSOCIATED NEURONAL CELL DEATH IN FRONTOTEMPORAL LOBAR DEGENERATION.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P661, doi. 10.1016/j.jalz.2017.06.790
- By:
- Publication type:
- Article
PET TAU IMAGING WITH AV-1451 IN MICROTUBULE ASSOCIATED PROTEIN TAU (MAPT) MUTATION CARRIERS RELATIVE TO ALZHEIMER’S DISEASE DEMENTIA AND CONTROLS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P131, doi. 10.1016/j.jalz.2016.06.211
- By:
- Publication type:
- Article
PET TAU IMAGING WITH AV-1451 IN MICROTUBULE-ASSOCIATED PROTEIN TAU (MAPT) MUTATION CARRIERS RELATIVE TO ALZHEIMER’S DISEASE DEMENTIA AND CONTROLS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P927, doi. 10.1016/j.jalz.2016.06.1918
- By:
- Publication type:
- Article
NEUROPSYCHOLOGICAL AND MRI FINDINGS IN MAPT MUTATION CARRIERS IN THE EVOLUTION FROM THE ASYMPTOMATIC TO SYMPTOMATIC STATE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P720, doi. 10.1016/j.jalz.2016.06.1416
- By:
- Publication type:
- Article
Longitudinal evaluation of familial frontotemporal dementia subjects (LEFFTDS): Subject characteristics, aims, and methodology.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P318, doi. 10.1016/j.jalz.2015.07.457
- By:
- Publication type:
- Article
Longitudinal mri and neuropsychological changes in symptomatic frontotemporal lobar degeneration subjects with mutations in mapt, pgrn, and c9orf72.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, p. P213, doi. 10.1016/j.jalz.2014.04.284
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- Publication type:
- Article
The neuropsychology of normal aging and preclinical Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, n. 1, p. 84, doi. 10.1016/j.jalz.2013.01.004
- By:
- Publication type:
- Article
Longitudinal gray and white matter changes in progranulin mutation carriers at risk for FTD: A VBM study
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Differentiating clinicopathologic and genetic aspects of hippocampal sclerosis in Alzheimer's disease from limbic predominant Alzheimer's disease and “pure” hippocampal sclerosis
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Anteromedial temporal lobe DTI and structural MRI changes in presymptomatic and symptomatic MAPT mutation carriers
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Characterization of frontotemporal dementia +/- amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Anteromedial temporal lobe diffusion tensor imaging and structural MRI changes in presymptomatic and symptomatic microtubule-associated protein tau (MAPT) mutation carriers
- Published in:
- 2012
- By:
- Publication type:
- Abstract