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High Frequency of Mutations in Four Different Disease Genes in Early-Onset Dementia.
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- Annals of the New York Academy of Sciences, 2000, v. 920, n. 1, p. 100, doi. 10.1111/j.1749-6632.2000.tb06910.x
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- Article
Modulation of Presenilin-1 Processing by Nitric Oxide during Apoptosis Induced by Serum Withdrawal and Glucose Deprivation.
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- Annals of the New York Academy of Sciences, 1999, v. 893, n. 1, p. 294, doi. 10.1111/j.1749-6632.1999.tb07840.x
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- Article
Cerebrospinal Fluid Biomarkers in Progranulin Mutations Carriers.
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- Journal of Alzheimer's Disease, 2011, v. 27, n. 4, p. 781, doi. 10.3233/JAD-2011-111046
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- Article
Role of OLR1 and Its Regulating hsa-miR369-3p in Alzheimer's Disease: Genetics and Expression Analysis.
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- Journal of Alzheimer's Disease, 2011, v. 26, n. 4, p. 787, doi. 10.3233/JAD-2011-110074
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- Article
A Novel MAPT Mutation Associated with the Clinical Phenotype of Progressive Nonfluent Aphasia.
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- Journal of Alzheimer's Disease, 2011, v. 26, n. 1, p. 19, doi. 10.3233/JAD-2011-102124
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- Article
An APOE Haplotype Associated with Decreased ε4 Expression Increases the Risk of Late Onset Alzheimer's Disease.
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- Journal of Alzheimer's Disease, 2011, v. 24, n. 2, p. 235, doi. 10.3233/JAD-2011-101764
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- Article
BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease.
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- Journal of Alzheimer's Disease, 2011, v. 23, n. 4, p. 701, doi. 10.3233/JAD-2010-101416
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- Article
Free Copper Distinguishes Mild Cognitive Impairment Subjects from Healthy Elderly Individuals.
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- Journal of Alzheimer's Disease, 2011, v. 23, n. 2, p. 239, doi. 10.3233/JAD-2010-101098
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- Article
A Novel Progranulin Mutation Causing Frontotemporal Lobar Degeneration with Heterogeneous Phenotypic Expression.
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- Journal of Alzheimer's Disease, 2011, v. 23, n. 1, p. 7, doi. 10.3233/JAD-2010-101461
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- Publication type:
- Article
Plasma Cystatin C and Risk of Developing Alzheimer's Disease in Subjects with Mild Cognitive Impairment.
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- Journal of Alzheimer's Disease, 2010, v. 22, n. 3, p. 985, doi. 10.3233/JAD-2010-101095
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- Publication type:
- Article
Failure to Replicate an Association of rs5984894 SNP in the PCDH11X Gene in a Collection of 1,222 Alzheimer's Disease Affected Patients.
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- Journal of Alzheimer's Disease, 2010, v. 21, n. 2, p. 385, doi. 10.3233/JAD-2010-091516
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- Article
FUS/TLS Genetic Variability in Sporadic Frontotemporal Lobar Degeneration.
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- Journal of Alzheimer's Disease, 2010, v. 19, n. 4, p. 1317, doi. 10.3233/JAD-2010-1328
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- Publication type:
- Article
The H1 Haplotype of the Tau Gene (MAPT) is Associated with Mild Cognitive Impairment.
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- Journal of Alzheimer's Disease, 2010, v. 19, n. 3, p. 909, doi. 10.3233/JAD-2010-1285
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- Publication type:
- Article
GRN Variability Contributes to Sporadic Frontotemporal Lobar Degeneration.
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- Journal of Alzheimer's Disease, 2010, v. 19, n. 1, p. 171, doi. 10.3233/JAD-2010-1225
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- Publication type:
- Article
Novel T719P AβPP Mutation Unbalances the Relative Proportion of Amyloid-β Peptides.
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- Journal of Alzheimer's Disease, 2009, v. 18, n. 2, p. 295, doi. 10.3233/JAD-2009-1142
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- Publication type:
- Article
Plasma Small Extracellular Vesicles with Complement Alterations in GRN / C9orf72 and Sporadic Frontotemporal Lobar Degeneration.
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- Cells (2073-4409), 2022, v. 11, n. 3, p. 488, doi. 10.3390/cells11030488
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- Article
Cerebrospinal Fluid EV Concentration and Size Are Altered in Alzheimer's Disease and Dementia with Lewy Bodies.
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- Cells (2073-4409), 2022, v. 11, n. 3, p. 462, doi. 10.3390/cells11030462
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- Article
A Multimodal Approach for Clinical Diagnosis and Treatment of Primary Progressive Aphasia (MAINSTREAM): A Study Protocol.
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- Brain Sciences (2076-3425), 2023, v. 13, n. 7, p. 1060, doi. 10.3390/brainsci13071060
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- Article
Long-lasting improvements in episodic memory among subjects with mild cognitive impairment who received transcranial direct current stimulation combined with cognitive treatment and telerehabilitation: a multicentre, randomized, active-controlled study.
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- Frontiers in Aging Neuroscience, 2024, p. 1, doi. 10.3389/fnagi.2024.1414593
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- Article
TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia.
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- Journal of Neurochemistry, 2013, v. 126, n. 6, p. 781, doi. 10.1111/jnc.12329
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- Article
Regional atrophy of transcallosal prefrontal connections in cognitively normal APOE ϵ4 carriers.
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- Journal of Magnetic Resonance Imaging, 2009, v. 29, n. 5, p. 1021, doi. 10.1002/jmri.21757
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- Article
HOXA1 A218G Polymorphism is Associated with Smaller Cerebellar Volume in Healthy Humans.
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- Journal of Neuroimaging, 2009, v. 19, n. 4, p. 353, doi. 10.1111/j.1552-6569.2008.00326.x
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- Publication type:
- Article
Blockade of the Tumor Necrosis Factor-Related Apoptosis Inducing Ligand Death Receptor DR5 Prevents β-Amyloid Neurotoxicity.
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- Neuropsychopharmacology, 2007, v. 32, n. 4, p. 872, doi. 10.1038/sj.npp.1301185
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- Article
Language training for oral and written naming impairment in primary progressive aphasia: a review.
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- Translational Neurodegeneration, 2021, v. 10, n. 1, p. 1, doi. 10.1186/s40035-021-00248-z
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- Article
Computed tomography in the detection of the vascular component in dementia.
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- 1995
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- Publication type:
- journal article
Behavioral and neurophysiological effects of transdermal rotigotine in atypical parkinsonism.
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- Frontiers in Neurology, 2014, v. 5, p. 1, doi. 10.3389/fneur.2014.00085
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- Article
Progranulin Mutations Affects Brain Oscillatory Activity in Fronto-Temporal Dementia.
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- Frontiers in Aging Neuroscience, 2016, p. 1, doi. 10.3389/fnagi.2016.00035
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- Article
Comparison of the effects of transdermal and oral rivastigmine on cognitive function and EEG markers in patients with Alzheimer's disease.
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- Frontiers in Aging Neuroscience, 2014, v. 6, p. 1, doi. 10.3389/fnagi.2014.00179
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- Article
Value of serum nonceruloplasmin copper for prediction of mild cognitive impairment conversion to Alzheimer disease.
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- Annals of Neurology, 2014, v. 75, n. 4, p. 574, doi. 10.1002/ana.24136
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- Article
Autophagy Markers Are Altered in Alzheimer's Disease, Dementia with Lewy Bodies and Frontotemporal Dementia.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 2, p. 1125, doi. 10.3390/ijms25021125
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- Article
The PINK1 p.Asn521Thr Variant Is Associated with Earlier Disease Onset in GRN/C9orf72 Frontotemporal Lobar Degeneration.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 21, p. 12847, doi. 10.3390/ijms232112847
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- Article
Plasma Small Extracellular Vesicle Cathepsin D Dysregulation in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 18, p. N.PAG, doi. 10.3390/ijms231810693
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- Article
Investigating the Endo-Lysosomal System in Major Neurocognitive Disorders Due to Alzheimer's Disease, Frontotemporal Lobar Degeneration and Lewy Body Disease: Evidence for SORL1 as a Cross-Disease Gene.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 24, p. 13633, doi. 10.3390/ijms222413633
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- Article
The Missing Heritability of Sporadic Frontotemporal Dementia: New Insights from Rare Variants in Neurodegenerative Candidate Genes.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 16, p. 3903, doi. 10.3390/ijms20163903
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- Article
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease.
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- Acta Neuropathologica, 2016, v. 132, n. 2, p. 213, doi. 10.1007/s00401-016-1566-9
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- Article
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.
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- Acta Neuropathologica, 2014, v. 128, n. 3, p. 397, doi. 10.1007/s00401-014-1298-7
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- Publication type:
- 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
H1 haplotype of the MAPT gene is associated with lower regional gray matter volume in healthy carriers.
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- European Journal of Human Genetics, 2009, v. 17, n. 3, p. 287, doi. 10.1038/ejhg.2008.185
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- Publication type:
- Article
Optimal Plasma Progranulin Cutoff Value for Predicting Null Progranulin Mutations in Neurodegenerative Diseases: A Multicenter Italian Study.
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- Neurodegenerative Diseases, 2012, v. 9, n. 3, p. 121, doi. 10.1159/000333132
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- Publication type:
- Article
Cerebrospinal Fluid Biomarkers for Alzheimer's Disease: The Present and the Future.
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- Neurodegenerative Diseases, 2011, v. 8, n. 6, p. 413, doi. 10.1159/000327756
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- Publication type:
- Article
Serum Beta-Secretase 1 Activity Is a Potential Marker for the Differential Diagnosis between Alzheimer's Disease and Frontotemporal Dementia: A Pilot Study.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 15, p. 8354, doi. 10.3390/ijms25158354
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- Publication type:
- Article
Unveiling New Genetic Variants Associated with Age at Onset in Alzheimer's Disease and Frontotemporal Lobar Degeneration Due to C9orf72 Repeat Expansions.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 13, p. 7457, doi. 10.3390/ijms25137457
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- Article
Incidence of young‐onset dementia in Italy: The Brescia register study.
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- Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2024, v. 16, n. 1, p. 1, doi. 10.1002/dad2.12544
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- Publication type:
- Article
Rotigotine is safe and efficacious in Atypical Parkinsonism Syndromes induced by both α-synucleinopathy and tauopathy.
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- Neuropsychiatric Disease & Treatment, 2014, v. 10, p. 1003, doi. 10.2147/NDT.S64015
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- Publication type:
- Article
Pattern of structural and functional brain abnormalities in asymptomatic granulin mutation carriers.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, n. 5, p. S354, doi. 10.1016/j.jalz.2013.09.009
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- Publication type:
- Article
The SIRT2 polymorphism rs10410544 and risk of Alzheimer’s disease in two Caucasian case–control cohorts.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2013, v. 9, n. 4, p. 392, doi. 10.1016/j.jalz.2012.02.003
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- Publication type:
- Article
Distribution of beta-amyloid peptides in leptomeningeal amyloid deposits and cerebrospinal fluid in patients with Alzheimer's disease: A mirror image
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- 2012
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- Abstract
Phenotypic heterogeneity of Alzheimer's disease: Toward the identification of molecular determinants underlying distinct clinicopathological subgroups
- Published in:
- 2012
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- Publication type:
- Abstract
Role of OLR1 and Its Regulating hsa-miR369-3p in Alzheimer’s Disease: Genetic and Expression Analysis
- Published in:
- 2011
- By:
- Publication type:
- Abstract
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
- Published in:
- 2011
- By:
- Publication type:
- Abstract