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Impaired glymphatic system in genetic frontotemporal dementia: a GENFI study.
- Published in:
- Brain Communications, 2024, v. 6, n. 4, p. 1, doi. 10.1093/braincomms/fcae185
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- Publication type:
- Article
A "glympse" into neurodegeneration: Diffusion MRI and cerebrospinal fluid aquaporin‐4 for the assessment of glymphatic system in Alzheimer's disease and other dementias.
- Published in:
- Human Brain Mapping, 2024, v. 45, n. 12, p. 1, doi. 10.1002/hbm.26805
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- Publication type:
- Article
Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation.
- Published in:
- 2017
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- Publication type:
- case study
Quantitative susceptibility mapping of the normal-appearing white matter as a potential new marker of disability progression in multiple sclerosis.
- Published in:
- European Radiology, 2023, v. 33, n. 8, p. 5368, doi. 10.1007/s00330-022-09338-6
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- Publication type:
- Article
From Genotype to Phenotype: Two Cases of Genetic Frontotemporal Lobar Degeneration with Premorbid Bipolar Disorder.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 27, n. 4, p. 791, doi. 10.3233/JAD-2011-110788
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- Publication type:
- Article
Cerebrospinal Fluid Biomarkers in Progranulin Mutations Carriers.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 27, n. 4, p. 781, doi. 10.3233/JAD-2011-111046
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- Publication type:
- Article
A Novel MAPT Mutation Associated with the Clinical Phenotype of Progressive Nonfluent Aphasia.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 26, n. 1, p. 19, doi. 10.3233/JAD-2011-102124
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- Publication type:
- Article
Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 24, n. 2, p. 253, doi. 10.3233/JAD-2011-101704
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- Publication type:
- Article
An APOE Haplotype Associated with Decreased ε4 Expression Increases the Risk of Late Onset Alzheimer's Disease.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 24, n. 2, p. 235, doi. 10.3233/JAD-2011-101764
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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.
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 21, n. 2, p. 385, doi. 10.3233/JAD-2010-091516
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- Publication type:
- Article
Osteopontin is Increased in the Cerebrospinal Fluid of Patients with Alzheimer's Disease and Its Levels Correlate with Cognitive Decline.
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 19, n. 4, p. 1143, doi. 10.3233/JAD-2010-1309
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- Publication type:
- Article
FUS/TLS Genetic Variability in Sporadic Frontotemporal Lobar Degeneration.
- Published in:
- 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.
- Published in:
- 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.
- Published in:
- 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
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.
- Published in:
- 2009
- By:
- Publication type:
- journal article
The Serotonin Transporter Promoter Polymorphic Region is not a Risk Factor for Alzheimer's Disease Related Behavioral Disturbances.
- Published in:
- Journal of Alzheimer's Disease, 2009, v. 18, n. 1, p. 125, doi. 10.3233/JAD-2009-1129
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- Publication type:
- Article
Modulation of MAPK- and PI3/AKT-Dependent Autophagy Signaling by Stavudine (D4T) in PBMC of Alzheimer's Disease Patients.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 14, p. N.PAG, doi. 10.3390/cells11142180
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- Publication type:
- Article
miR-150-5p and let-7b-5p in Blood Myeloid Extracellular Vesicles Track Cognitive Symptoms in Patients with Multiple Sclerosis.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 9, p. N.PAG, doi. 10.3390/cells11091551
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- Publication type:
- Article
Extracellular Vesicles in Multiple Sclerosis: Role in the Pathogenesis and Potential Usefulness as Biomarkers and Therapeutic Tools.
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 7, p. 1733, doi. 10.3390/cells10071733
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- Publication type:
- Article
MiRNA Profiling in Plasma Neural-Derived Small Extracellular Vesicles from Patients with Alzheimer's Disease.
- Published in:
- Cells (2073-4409), 2020, v. 9, n. 6, p. 1443, doi. 10.3390/cells9061443
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- Publication type:
- Article
Untangling Extracellular Proteasome-Osteopontin Circuit Dynamics in Multiple Sclerosis.
- Published in:
- Cells (2073-4409), 2019, v. 8, n. 3, p. 262, doi. 10.3390/cells8030262
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- Publication type:
- Article
A Multimodal Approach for Clinical Diagnosis and Treatment of Primary Progressive Aphasia (MAINSTREAM): A Study Protocol.
- Published in:
- Brain Sciences (2076-3425), 2023, v. 13, n. 7, p. 1060, doi. 10.3390/brainsci13071060
- By:
- Publication type:
- Article
Alemtuzumab in multiple sclerosis during the COVID-19 pandemic: A mild uncomplicated infection despite intense immunosuppression.
- Published in:
- 2020
- By:
- Publication type:
- Letter
T cells producing GM-CSF and IL-13 are enriched in the cerebrospinal fluid of relapsing MS patients.
- Published in:
- Multiple Sclerosis Journal, 2020, v. 26, n. 10, p. 1172, doi. 10.1177/1352458519852092
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- Publication type:
- Article
CSF β-amyloid predicts prognosis in patients with multiple sclerosis.
- Published in:
- Multiple Sclerosis Journal, 2019, v. 25, n. 9, p. 1223, doi. 10.1177/1352458518791709
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- Publication type:
- Article
The loss of macular ganglion cells begins from the early stages of disease and correlates with brain atrophy in multiple sclerosis patients.
- Published in:
- Multiple Sclerosis Journal, 2019, v. 25, n. 1, p. 31, doi. 10.1177/1352458517740214
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- Publication type:
- Article
Aquaporin-4 cerebrospinal fluid levels are higher in neurodegenerative dementia: looking at glymphatic system dysregulation.
- Published in:
- Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-022-01077-6
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- Publication type:
- Article
Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia.
- Published in:
- Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-022-01042-3
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- Publication type:
- Article
Amyloid PET imaging and dementias: potential applications in detecting and quantifying early white matter damage.
- Published in:
- Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-021-00933-1
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- Publication type:
- Article
Cognitive composites for genetic frontotemporal dementia: GENFI-Cog.
- Published in:
- Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-022-00958-0
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- Publication type:
- Article
The Revised Self-Monitoring Scale detects early impairment of social cognition in genetic frontotemporal dementia within the GENFI cohort.
- Published in:
- Alzheimer's Research & Therapy, 2021, v. 13, p. 1, doi. 10.1186/s13195-021-00865-w
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- Publication type:
- Article
Structural and metabolic cerebral alterations between elderly bipolar disorder and behavioural variant frontotemporal dementia: A combined MRI-PET study.
- Published in:
- Australian & New Zealand Journal of Psychiatry, 2019, v. 53, n. 5, p. 413, doi. 10.1177/0004867418815976
- By:
- Publication type:
- Article
Loss of function mutations in the progranulin gene are related to pro-inflammatory cytokine dysregulation in frontotemporal lobar degeneration patients.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series.
- Published in:
- Neurogenetics, 2008, v. 9, n. 3, p. 197, doi. 10.1007/s10048-008-0127-3
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- Publication type:
- Article
Comparison of arterial spin labeling registration strategies in the multi-center GENetic frontotemporal dementia initiative (GENFI).
- Published in:
- 2018
- By:
- Publication type:
- journal article
Association study to evaluate the serotonin transporter and apolipoprotein E genes in frontotemporal lobar degeneration in Italy.
- Published in:
- Journal of Human Genetics, 2008, v. 53, n. 11/12, p. 1029, doi. 10.1007/s10038-008-0344-5
- By:
- Publication type:
- Article
CSF β-amyloid as a putative biomarker of disease progression in multiple sclerosis.
- Published in:
- Multiple Sclerosis Journal, 2017, v. 23, n. 8, p. 1085, doi. 10.1177/1352458516674566
- By:
- Publication type:
- Article
Progranulin genetic polymorphisms influence progression of disability and relapse recovery in multiple sclerosis.
- Published in:
- Multiple Sclerosis Journal, 2016, v. 22, n. 8, p. 1007, doi. 10.1177/1352458515610646
- By:
- Publication type:
- Article
Brain temperature in multiple sclerosis.
- Published in:
- 2014
- By:
- Publication type:
- Letter to the Editor
Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis.
- Published in:
- Multiple Sclerosis Journal, 2013, v. 19, n. 14, p. 1938, doi. 10.1177/1352458513485654
- By:
- Publication type:
- Article
Consensus definitions and application guidelines for control groups in cerebrospinal fluid biomarker studies in multiple sclerosis.
- Published in:
- Multiple Sclerosis Journal, 2013, v. 19, n. 13, p. 1802, doi. 10.1177/1352458513488232
- By:
- Publication type:
- Article
Multiple sclerosis: BAFF and CXCL13 in cerebrospinal fluid.
- Published in:
- Multiple Sclerosis Journal, 2011, v. 17, n. 7, p. 819, doi. 10.1177/1352458511398887
- By:
- Publication type:
- Article
Hypermethylation of the CpG-island near the C9orf72 G4C2-repeat expansion in FTLD patients.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 21, p. 5630, doi. 10.1093/hmg/ddu279
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- Publication type:
- Article
Next generation sequencing in sporadic retinoblastoma patients reveals somatic mosaicism.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 11, p. 1523, doi. 10.1038/ejhg.2015.6
- By:
- Publication type:
- Article
Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there?
- Published in:
- Internal & Emergency Medicine, 2021, v. 16, n. 5, p. 1247, doi. 10.1007/s11739-021-02634-x
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- Publication type:
- Article
Altered plasma protein profiles in genetic FTD – a GENFI study.
- Published in:
- Molecular Neurodegeneration, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13024-023-00677-6
- By:
- Publication type:
- Article
Neurodevelopmental effects of genetic frontotemporal dementia in young adult mutation carriers.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 5, p. 2120, doi. 10.1093/brain/awac446
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- Publication type:
- Article
Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementia.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 1, p. 321, doi. 10.1093/brain/awac069
- By:
- Publication type:
- Article
A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Neurofilament light chain and oligoclonal bands are prognostic biomarkers in radiologically isolated syndrome.
- Published in:
- 2018
- By:
- Publication type:
- journal article